Skip to main content
Advertisement

Main menu

  • Home
  • Content
    • Current Issue
    • Accepted Manuscripts
    • Article Preview
    • Past Issue Archive
    • Video Articles
    • AJNR Case Collection
    • Case of the Week Archive
    • Case of the Month Archive
    • Classic Case Archive
  • Special Collections
    • AJNR Awards
    • Low-Field MRI
    • Alzheimer Disease
    • ASNR Foundation Special Collection
    • Photon-Counting CT
    • View All
  • Multimedia
    • AJNR Podcasts
    • AJNR SCANtastic
    • Trainee Corner
    • MRI Safety Corner
    • Imaging Protocols
  • For Authors
    • Submit a Manuscript
    • Submit a Video Article
    • Submit an eLetter to the Editor/Response
    • Manuscript Submission Guidelines
    • Statistical Tips
    • Fast Publishing of Accepted Manuscripts
    • Graphical Abstract Preparation
    • Imaging Protocol Submission
    • Author Policies
  • About Us
    • About AJNR
    • Editorial Board
    • Editorial Board Alumni
  • More
    • Become a Reviewer/Academy of Reviewers
    • Subscribers
    • Permissions
    • Alerts
    • Feedback
    • Advertisers
    • ASNR Home

User menu

  • Alerts
  • Log in

Search

  • Advanced search
American Journal of Neuroradiology
American Journal of Neuroradiology

American Journal of Neuroradiology

ASHNR American Society of Functional Neuroradiology ASHNR American Society of Pediatric Neuroradiology ASSR
  • Alerts
  • Log in

Advanced Search

  • Home
  • Content
    • Current Issue
    • Accepted Manuscripts
    • Article Preview
    • Past Issue Archive
    • Video Articles
    • AJNR Case Collection
    • Case of the Week Archive
    • Case of the Month Archive
    • Classic Case Archive
  • Special Collections
    • AJNR Awards
    • Low-Field MRI
    • Alzheimer Disease
    • ASNR Foundation Special Collection
    • Photon-Counting CT
    • View All
  • Multimedia
    • AJNR Podcasts
    • AJNR SCANtastic
    • Trainee Corner
    • MRI Safety Corner
    • Imaging Protocols
  • For Authors
    • Submit a Manuscript
    • Submit a Video Article
    • Submit an eLetter to the Editor/Response
    • Manuscript Submission Guidelines
    • Statistical Tips
    • Fast Publishing of Accepted Manuscripts
    • Graphical Abstract Preparation
    • Imaging Protocol Submission
    • Author Policies
  • About Us
    • About AJNR
    • Editorial Board
    • Editorial Board Alumni
  • More
    • Become a Reviewer/Academy of Reviewers
    • Subscribers
    • Permissions
    • Alerts
    • Feedback
    • Advertisers
    • ASNR Home
  • Follow AJNR on Twitter
  • Visit AJNR on Facebook
  • Follow AJNR on Instagram
  • Join AJNR on LinkedIn
  • RSS Feeds

AJNR Awards, New Junior Editors, and more. Read the latest AJNR updates

OtherNeuroimaging Physics/Functional Neuroimaging/CT and MRI Technology

Recommended Resting-State fMRI Acquisition and Preprocessing Steps for Preoperative Mapping of Language and Motor and Visual Areas in Adult and Pediatric Patients with Brain Tumors and Epilepsy

V.A. Kumar, J. Lee, H.-L. Liu, J.W. Allen, C.G. Filippi, A.I. Holodny, K. Hsu, R. Jain, M.P. McAndrews, K.K. Peck, G. Shah, J.S. Shimony, S. Singh, M. Zeineh, J. Tanabe, B. Vachha, A. Vossough, K. Welker, C. Whitlow, M. Wintermark, G. Zaharchuk and H.I. Sair
American Journal of Neuroradiology February 2024, 45 (2) 139-148; DOI: https://doi.org/10.3174/ajnr.A8067
V.A. Kumar
aFrom the The University of Texas MD Anderson Cancer Center (V.A.K., J.L., H.-L.L., M.W.), Houston, Texas
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for V.A. Kumar
J. Lee
aFrom the The University of Texas MD Anderson Cancer Center (V.A.K., J.L., H.-L.L., M.W.), Houston, Texas
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for J. Lee
H.-L. Liu
aFrom the The University of Texas MD Anderson Cancer Center (V.A.K., J.L., H.-L.L., M.W.), Houston, Texas
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for H.-L. Liu
J.W. Allen
bEmory University (J.W.A.), Atlanta, Georgia
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for J.W. Allen
C.G. Filippi
cTufts University (C.G.F.), Boston, Massachusetts
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for C.G. Filippi
A.I. Holodny
dMemorial Sloan Kettering Cancer Center (A.I.H., K.K.P.), New York, New York
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for A.I. Holodny
K. Hsu
eNew York University (K.H., R.J.), New York, New York
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for K. Hsu
R. Jain
eNew York University (K.H., R.J.), New York, New York
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
M.P. McAndrews
fUniversity of Toronto (M.P.M.), Toronto, Ontario, Canada
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
K.K. Peck
dMemorial Sloan Kettering Cancer Center (A.I.H., K.K.P.), New York, New York
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for K.K. Peck
G. Shah
gUniversity of Michigan (G.S.), Ann Arbor, Michigan
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for G. Shah
J.S. Shimony
hWashington University School of Medicine (J.S.S.), St. Louis, Missouri
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for J.S. Shimony
S. Singh
iUniversity of Texas Southwestern Medical Center (S.S.), Dallas, Texas
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
M. Zeineh
jStanford University (M.Z., G.Z.), Palo Alto, California
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for M. Zeineh
J. Tanabe
kUniversity of Colorado (J.T.), Aurora, Colorado
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for J. Tanabe
B. Vachha
lUniversity of Massachusetts (B.V.), Worcester, Massachusetts
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for B. Vachha
A. Vossough
mChildren’s Hospital of Philadelphia, University of Pennsylvania (A.V.), Philadelphia, Pennsylvania
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for A. Vossough
K. Welker
nMayo Clinic (K.W.), Rochester, Minnesota
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for K. Welker
C. Whitlow
oWake Forest University (C.W.), Winston-Salem, North Carolina
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for C. Whitlow
M. Wintermark
aFrom the The University of Texas MD Anderson Cancer Center (V.A.K., J.L., H.-L.L., M.W.), Houston, Texas
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for M. Wintermark
G. Zaharchuk
jStanford University (M.Z., G.Z.), Palo Alto, California
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for G. Zaharchuk
H.I. Sair
pJohns Hopkins University (H.I.S.), Baltimore, Maryland.
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • ORCID record for H.I. Sair
  • Article
  • Figures & Data
  • Info & Metrics
  • Responses
  • References
  • PDF
Loading

Abstract

Resting-state (rs) fMRI has been shown to be useful for preoperative mapping of functional areas in patients with brain tumors and epilepsy. However, its lack of standardization limits its widespread use and hinders multicenter collaboration. The American Society of Functional Neuroradiology, American Society of Pediatric Neuroradiology, and the American Society of Neuroradiology Functional and Diffusion MR Imaging Study Group recommend specific rs-fMRI acquisition approaches and preprocessing steps that will further support rs-fMRI for future clinical use. A task force with expertise in fMRI from multiple institutions provided recommendations on the rs-fMRI steps needed for mapping of language, motor, and visual areas in adult and pediatric patients with brain tumor and epilepsy. These were based on an extensive literature review and expert consensus.

Following rs-fMRI acquisition parameters are recommended: minimum 6-minute acquisition time; scan with eyes open with fixation; obtain rs-fMRI before both task-based fMRI and contrast administration; temporal resolution of ≤2 seconds; scanner field strength of 3T or higher. The following rs-fMRI preprocessing steps and parameters are recommended: motion correction (seed-based correlation analysis [SBC], independent component analysis [ICA]); despiking (SBC); volume censoring (SBC, ICA); nuisance regression of CSF and white matter signals (SBC); head motion regression (SBC, ICA); bandpass filtering (SBC, ICA); and spatial smoothing with a kernel size that is twice the effective voxel size (SBC, ICA).

The consensus recommendations put forth for rs-fMRI acquisition and preprocessing steps will aid in standardization of practice and guide rs-fMRI program development across institutions. Standardized rs-fMRI protocols and processing pipelines are essential for multicenter trials and to implement rs-fMRI as part of standard clinical practice.

ABBREVIATIONS:

BOLD
blood oxygenation level–dependent
EC
eyes closed
EO-F
eyes open with fixation
EO
eyes open without fixation
FC
functional connectivity
GSR
global signal regression
ICA
independent component analysis
rs
resting-state
rs-FC
rs-functional connectivity
RSN
resting-state networks
SBC
seed-based correlation analysis
STC
slice timing correction
tb
task-based
TR
repetition time

Resting-state (rs) fMRI has been found promising for presurgical mapping of eloquent brain areas for brain tumor and epilepsy surgery.1 For example, rs-fMRI is beneficial in localizing language areas when task-based (tb) fMRI cannot be performed due to cognitive impairment or limited tb-fMRI.2 However, more studies are needed to validate the clinical utility of rs-fMRI for preoperative localization of language in adults and pediatric patients.

Rs-fMRI can be performed while the patient is at rest, and it can be acquired without the need for highly trained personnel. However, rs-fMRI is more susceptible to head motion than tb-fMRI.3,4 It is critical to specify rs-fMRI acquisition and preprocessing steps and parameters to isolate the blood oxygen level-dependent (BOLD) signal corresponding to networks of interest. Additionally, not all preprocessing steps may be needed because some potentially carry the risk of removing the intrinsic BOLD signal.3

Yet, there is no standardization of rs-fMRI acquisition and preprocessing steps across institutions, hindering data sharing, comparison of results, and scientific transparency. Therefore, an expert task force consisting of 16 neuroradiologists, 2 pediatric neuroradiologists, 2 imaging physicists, and 1 clinical neuropsychologist with expertise in fMRI was formed to provide recommendations for specific rs-fMRI acquisition and preprocessing steps based on literature review and expert consensus for presurgical mapping of language, motor, and visual areas in patients with brain tumor and epilepsy. This task force hopes to encourage multicenter studies to implement rs-fMRI for widespread clinical use. Unlike tb-fMRI,5 our recommendations can be used for both adult and pediatric patients.

LITERATURE SEARCH STRATEGY AND REVIEW PROCESS

References were identified through a literature search on PubMed and the Web of Science using the following keywords: (functional connectivity OR resting state OR resting-state) AND (fMRI OR functional MR imaging OR functional MR imaging) AND (brain neoplasm OR brain tumor OR epilepsy) AND (motor OR sensorimotor OR language OR visual OR vision) in July 2022. Although in some publications, the terms are used interchangeably, for the purpose of this article, rs-fMRI refers to BOLD signal acquisition during rest and rs-functional connectivity (rs-FC) refers to postprocessed resting-state correlation results. Rs-FC data are often represented as resting-state networks (RSN) of closely connected areas across the brain (eg, language).

From the total of 1291 articles that were identified from the initial keyword search, 305 duplicate articles were removed. The abstracts of the remaining 986 articles were evaluated and further subselected for the following criteria: rs-fMRI studies written in English that localized and/or lateralized individual language, motor, and/or visual areas in patients with brain tumor and/or epilepsy for preoperative planning from January 2008 until July 2022. Studies that used rs-fMRI to localize seizure-onset zones to examine connectome or local properties of the rs-fMRI signal with an amplitude of low-frequency fluctuation and regional homogeneity analysis without localizing functional areas were excluded. A total of 75 articles met the inclusion criteria.

All the acquisition and preprocessing steps that each article used were recorded. For articles that used >1 parameter for a step, they would be counted more than once for analysis. For example, if an article used 2 different temporal resolutions, this article would be counted as 2 different studies. Articles that used a near-equivalent number of patients with brain tumor and epilepsy would also be counted as 2 distinct studies. Additionally, when we recorded the number of studies that used specific preprocessing steps, they were separated on the basis of whether they used seed-based correlation analysis (SBC), independent component analysis (ICA), and/or other algorithms such as multilayer perceptron, cortical parcellation, or deep learning analysis. If articles used >1 type of algorithm, they would be included in the analysis more than once. Thus, a total of 86 studies were used for the literature review. In addition, for articles that did not report the length of the scan, this was calculated by multiplying the temporal resolution used by the number of volumes scanned.

Individuals with expertise in fMRI were invited to form a task force to reach expert consensus on the specific rs-fMRI acquisition and preprocessing steps for presurgical planning in patients with brain tumors and epilepsy (Tables 1 and 2). Across a total of 4 Webinar meetings, the task force members anonymously voted on every acquisition and preprocessing step after presentation of the literature review and after the ensuing group discussion. On the basis of a Delphi method, expert consensus was reached when ≥60% of the members recommended a specific acquisition/preprocessing step.6 The parameters that were not recommended were deemed optional. Subsequently, 2 American Society of Pediatric Neuroradiology neuroradiologists with expertise in pediatric fMRI were invited to provide additional input as it related to pediatric rs-fMRI.

View this table:
  • View inline
  • View popup
Table 1:

Resting-state fMRI acquisition parameters

View this table:
  • View inline
  • View popup
Table 2:

Resting-state fMRI preprocessing steps

RECOMMENDATIONS OF ACQUISITION AND PREPROCESSING STEPS

Acquisition Steps

Length of Scan: Recommend Minimum of 6 Minutes.

Because the scan acquisition time for rs-fMRI can influence the sensitivity, reliability, and stability for detecting rs-FC, determining the appropriate scan length is important. The task force recommends a minimum rs-fMRI scan time of 6 minutes for preoperative mapping of the motor, language, and visual areas in patients with brain tumor and epilepsy.

The reliability, consistency, and strength of rs-fMRI increases with scan duration. Birn et al7 have shown that the reliability across the 153 rs-FCs increased with scan duration and demonstrated improvement in the intrasession reliability of rs-fMRI FC by 20% at 12 versus 6 minutes. An even greater improvement in intrasession reliability was noted at 6 minutes (intraclass correlation coefficient = 0.4) compared with 3 minutes (intraclass correlation coefficient = 0.2).7 Stronger reliability of the functional connectivity (FC) was noted with increased scan acquisition, but this improvement plateaued at around 13 minutes.7 However, these studies were conducted on healthy subjects.

For patients with neurologic deficits who need mapping of large cortical areas, shorter scan duration may be more clinically optimal.8 In most preoperative MR imaging examinations, patients need to undergo scanning for extended periods of time to include anatomic registration images, tb-fMRI, DTI, and other clinical sequences, and lying still in a scanner will likely be tiring and uncomfortable, especially for patients who are claustrophobic.8 Furthermore, longer scan times could increase the chance of excessive head motion and patients falling asleep. Six minutes of scanning time was shown to be sufficient for the correlation strengths within and between major RSNs to stabilize in healthy participants, with only minimal benefits beyond this duration.9 Even shorter scan times, approximately 3–4 minutes, have been shown to reliably detect motor and language areas, using a high-speed multiband acquisition with a very short (eg, <500 ms) temporal resolution in patients with glioma.10

For the purposes of presurgical mapping of motor, language, and visual areas, we thus recommend a minimum of 6 minutes of scan time, acknowledging that more scan time may be needed to map other rs-fMRI networks. From our literature review, 79/86 (92%) studies reported the scan length per session that they used. The mean, mode, and median scan lengths per session were the following: 7, 6, and 6.1 minutes with the scan length ranging from 4.3 to 28 minutes. In addition to reporting the total length of the scan, we chose to report the scanning time by the length of scan per session: 67/79 (85%) studies had 1 rs-fMRI acquisition session, 9/79 (11%) studies had 2 rs-fMRI sessions, and 3/79 (4%) had 4 rs-fMRI sessions. Thus, on the basis of the literature review, most of the studies used only 1 rs-fMRI acquisition session.

Eye Status: Recommend Eyes Open with Fixation.

Three eye status conditions during presurgical rs-fMRI were considered: eyes closed (EC), eyes open with fixation (EO-F), and eyes open without fixation (EO). The specific eye status condition can impact the strength, reliability, and consistency of rs-FC.11 As discussed below, the task force recommends EO-F, typically to a crosshair. At institutions that cannot accommodate EO-F, the EC is considered acceptable for presurgical planning.

Patients closing their eyes during a rs-fMRI scan increases their risk of falling asleep.12,13 Tagliazucchi et al13 demonstrated in 71 healthy subjects with EC during a rs-fMRI scan that after 4 minutes of scanning, one-third of the participants fell asleep, and within 10 minutes, one-half were asleep. However, in EO-F, they stayed awake longer compared with either EC or EO.13 Most importantly, Tagliazucchi et al showed changes in rs-FC in various brain areas, including the sensorimotor and visual areas, during sleep compared with the awake state.13 Furthermore, Wang et al14 showed that being awake increased test-retest reliability across various RSNs, including the somatomotor and visual networks. Furthermore, Agcaoglu et al15 noted that the EC condition likely led to subjects being drowsy and daydreaming, which led to more variability and no interactions with demographic covariates in contrast to the EO-F condition.

Conversely, the EC and EO states are considered true resting states and not as cognitively demanding as EO-F.16 Additionally, multiple studies have shown that variability in the strength or reliability of the FC of sensorimotor15,17,18 and visual11,16,17 networks to other networks depends on the eye status condition. While this result would be a factor to consider if we were to quantify or analyze FC, for the purpose of preoperative mapping of cortical areas, ensuring that the patients are awake and minimizing movement should be emphasized. In this regard, both the EC and EO are less favorable because of potential excess eye movement during the scan compared with EO-F.11 In EC, patients falling asleep could lead to excessive head motion.

From our literature review, 70/86 (81%) studies reported the eye status condition of their patients. Thirty-five of 70 (50%) studies had their patients close their eyes, 24/70 (34%) studies had patients fixate their eyes on a crosshair, 6/70 (8.6%) studies had patients open eyes without fixation, and 5/70 (7.1%) studies had sedated patients. More rs-fMRI studies using the eyes closed condition may be because it is logistically easier than displaying a crosshair.

Order of rs-fMRI versus tb-fMRI: Recommend rs-fMRI before tb-fMRI.

The task force recommends that rs-fMRI be obtained before tb-fMRI when feasible. The FC of rs-areas can be influenced by tasks.19,20 Wang et al19 reported changes in the nodal degree and global efficiency across intra- and extra-default mode areas and FC during the posttask relative to pretask resting states in healthy participants. Tung et al20 noted a transient (5 minute) effect of increased FC between the motor cortex in the post-motor task resting state compared with pretask.20 This effect was not noted in the control group. Because tb-fMRI protocols can vary among patients and institutions, having patients undergo rs-fMRI and then tb-fMRI will allow better standardization for multicenter studies. Furthermore, because rs-fMRI is more sensitive to motion artifacts than tb-fMRI,4 acquiring it near the start of the imaging session would reduce the chance of these artifacts. Nevertheless, if tb-fMRI needs to be obtained before rs-fMRI due to established institutional protocols and subject limitations, it is the opinion of the task force that rs-fMRI can still be analyzed. A compromise is that other structural imaging such as DTI can be performed between tb- and rs-fMRI acquisitions to minimize potential tb-fMRI influences on rs-fMRI FC.

From our literature review, 58/86 (67%) studies reported using both rs-fMRI and tb-fMRI paradigms. Twenty-six of 58 studies (45%) reported a specific order in which they performed both fMRI scans. Eighteen of 26 (69%) studies acquired rs-fMRI before tb-fMRI paradigms, whereas 8/26 (31%) studies performed tb-fMRI before rs-fMRI.

Repetition time (TR): Recommend TR of ≤2 Seconds.

For rs-fMRI, using a single-shot EPI sequence is most common. TR defines the repetition time or the rate of sampling of the low-frequency rs-BOLD signal fluctuation. The task force recommends a TR of ≤2 seconds.

An accelerated TR can improve the discrimination of different components with ICA because of the increase in temporal information.21 The Human Connectome Project (https://www.humanconnectome.org/) used a TR of 0.7 seconds to scan 1200 controls, improving identification of resting-state signal fluctuations and increasing their ability to detect physiologic noise.22 Voets et al23 reported similar findings and compared the use of 3 different temporal sampling rates at 0.72, 1.56 , and 3.5 seconds to localize the motor region in patients with gliomas. Using a TR of <2 seconds compared with 3.5 seconds resulted in greater success in localizing and spatially separating the motor region into its 3 functional zones.23 Additionally, a long TR of >4–5 seconds approaches the Nyquist limit frequency for typical BOLD frequencies (<0.1 Hz). Using simulated tb-fMRI, Parker et al24 observed a decrease in t-statistics with longer TRs.24 The gain in t-statistics due to the slice timing correction (STC) was negligible at a TR of <2 seconds compared with a TR of >2 sections (see STC correction below).

In modern scanners, multiband acquisition allows shorter TR while maintaining whole-brain coverage, which can increase rs-fMRI sensitivity21 and statistical power. If one is not using simultaneous multislice scanning, shortening the TR will compromise the spatial resolution or section coverage.22 Multislice scanning capability may not be readily available on clinical scanners at this time.

From our literature review, 85/86 (99%) studies reported the TR they used. The mean, mode, and median TRs were the following: 2.2, 2, and 2 seconds with the TR ranging from 0.14 to 5 seconds.

Physiologic Noise-Source Monitoring: Optional.

Physiologic noise-source monitoring of cardiac and respiratory origins aims to remove low-frequency physiologic fluctuations unrelated to neuronal activity that could introduce artifacts and decrease the sensitivity of rs-fMRI.25 The 2 main sources of physiologic fluctuations are heart-related variations, typically around 0.9–1.2 Hz, and respiratory variations, around 0.2–0.4 Hz,26 which can be detected via photoplethysmography on the index finger and a pneumatic belt around the abdomen, respectively.27 Cardiac pulsations can cause CSF and brain parenchymal movement, which can cause changes in the BOLD fMRI series, specifically in the vertebrobasilar system.26 Respiratory movement can affect rs-fMRI.26 The task force considers physiologic noise monitoring optional.

Although physiologic recording correction for physiologic variations is possible using retrospective correction techniques like RETROICOR,28 the signal variation can also be minimized through a combination of appropriate data-preprocessing steps.9 RETROICOR can suppress both cardiac and respiratory fluctuations by 68% and 50%, respectively.28 Finite impulse response band-reject digital filters and retrospective gating in k-space using data-driven algorithms can also remove cardiac and respiratory fluctuations.26 However, these steps require external physiologic monitoring, which would be additional steps that could unnecessarily lengthen the fMRI procedure in the clinic. In contrast, there are software solutions that do not require such external monitoring. For example, Behzadi et al29 have shown that by using anatomic component correction, cardiac and respiratory noise can be simultaneously removed by conducting white matter and CSF regression without external monitoring. Van Dijk et al9 showed that regressing nuisance correlations from white matter, ventricular, and whole-brain signals can adequately remove artifacts from cardiorespiratory sources. Bandpass filtering out low-frequency fluctuations can also remove physiologic fluctuations. Separating noise components with independent component analysis could offer additional correction.30

Monitoring physiologic noise for removal may be helpful in patients anticipated to have excessive physiologic variation, such as pediatric patients or those with movement disorders. Notably, variations in respiration could be <0.1 Hz, which overlaps with BOLD signal fluctuations between 0.01 and 0.1 Hz,9,25 precluding straightforward removal by bandpass filtering. However, even in the situation above, using a short TR, ICA, or a combination of various preprocessing techniques, such as nuisance regression9 or global signal regression,31 can reduce the noise contributions and make it feasible to detect the rs-BOLD signal relevant to preoperative mapping of rs-FC. In multislice fMRI data, physiologic noise sources at greater frequencies than the expected bandwidth of rs-fMRI BOLD fluctuations can, through undersampling, be aliased down into the target signal band.32

Two of 86 (2.3%) studies in our literature review externally monitored and adjusted for cardiac and respiratory sources of variation in the BOLD signal.

Gadolinium-Based Contrast Agent Administration: Recommend rs-fMRI before Contrast Administration.

There is limited literature support for IV administration of gadolinium-based contrast agents before or after rs-fMRI. Clinical decisions on when to administer gadolinium-based contrast agent will typically depend on institutional policy, experience, and/or the purpose of the fMRI scan. In a tb-fMRI study, Naganawa et al33 showed that administering gadolinium-based contrast agents decreased the sensitivity at which the primary motor cortex could be localized in 8 healthy participants who underwent a self-paced motor task compared with precontrast imaging.

The task force recommends obtaining the rs-fMRI scan before contrast administration. However, in cases in which a patient’s standard-of-care imaging needs to be prioritized and information gleaned from rs-fMRI might be helpful, postcontrast rs-fMRI data could still be interpreted with caution. This suggestion is especially relevant in cases in which the patient may not be able to complete the entire scan.

Scanner Field Strength: Recommend 3T or Higher.

Based on the literature review, the most common MR imaging field strength used for rs-fMRI is 3T. Scanners of all 3 field strengths (1.5T, 3T, and 7T) can be used for preoperative mapping of rs-areas. Scanners with higher field strengths produce higher SNRs, which can be used to achieve higher spatial resolution.34 Additionally, the greater magnetic susceptibility effects at higher magnetic field strengths increase the expected BOLD signal change. Garcia-Eulate et al35 showed that 3T MR imaging showed improved localization of the motor and somatosensory areas with rs-fMRI compared with 1.5T. Krasnow et al36 also determined activation in several regions such as the inferior frontal gyrus, orbitofrontal gyrus, and lingual gyrus with 3T, which could not be detected with 1.5T.

Compared with 3T, a 7T study has shown more precise mapping of RSNs,37 and another study showed that the measured rs-fMRI signal increased almost 2-fold.38 However, not only is 7T less widely available than 3T, it can introduce more physiologic, motion, and susceptibility artifacts.34 If a patient has implants that are MR imaging–conditional at only 1.5T or metal objects that are expected to cause susceptibility artifacts near the functional areas of interest, then 1.5T may be preferable.

From our literature review, 85/86 (99%) studies that used rs-fMRI for presurgical mapping reported the scanner field strength used. Seventy-five of 85 (88%) studies acquired rs-fMRI with 3T scanners, 9/85 (11%) studies used 1.5T scanners, and 1/85 (1.2%) studies used a 7T scanner.

Preprocessing Steps

Motion Correction: Recommended for Both SBC and ICA.

Motion correction involves spatially realigning the dynamic volumes acquired during the rs-fMRI scan to a reference volume that is usually the first or the middle volume of the scan.39 The task force recommends including motion correction as a preprocessing step for both SBC and ICA.

Head movement, even in the order of millimeters, can prevent accurate rs-fMRI estimates.3 Head motion can cause a change in tissue composition within a voxel, which can, in turn, affect its net magnetization and introduce spin-history artifacts that could be difficult to distinguish from true rs-fMRI signal.3 Head motion introduces distance-dependent bias,40 in which movement can increase BOLD signal changes in certain regions of the brain but cause a decrease in others.41 Finally, head motion can introduce BOLD signals that may not be distinguishable from neural activity,3 contributing to false-positive connections. Especially with the high susceptibility to motion artifacts of rs-fMRI, motion correction is essential to improve its sensitivity3 and specificity.42

Jo et al40 showed a decrease in distance-dependent correlation bias after motion correction.40 Maknojia et al3 noted that motion correction was essential to isolate true rs-networks from noise, and Beall et al43 showed a reduced image temporal standard deviation (SD) after motion correction. Additionally, motion parameters can be included in the general linear model for nuisance regression.44 Oakes et al42 did a comparative analysis of commonly used software programs such as Analysis of Functional Neuro Images (AFNI; http://afni.nimh.nih.gov/afni), SPM (http://www.fil.ion.ucl.ac.uk/spm/software/spm12), FSL http://www.fmrib.ox.ac.uk/fsl, AIR,45,46 and BrainVoyager (https://www.brainvoyager.com/bv/doc/UsersGuide/BrainVoyagerUsersGuide.html) and concluded that all performed equivalently.

While motion correction can improve data quality, it cannot negate all the effects of head motion.27,47 Head motion control should be emphasized to the patients being scanned. Additionally, other preprocessing techniques such as despiking, volume censoring, and/or head motion regression should additionally be considered.27

All the studies in our literature review, including those that used SBC, ICA, and other methods, conducted motion correction (100%, 86/86).

STC: Optional at a TR of ≤2 Seconds; Recommended at a TR of >2 Seconds for Both SBC and ICA.

The majority of fMRI studies use a 2D multislice single-shot gradient-echo EPI sequence. Because the slices are acquired via a sequential or interleaved mode, each section is acquired at a different time within the TR.24 These time differences cause temporal shifts in the data, which could result in a mismatch between the measured-versus-actual hemodynamic response.48 STC accounts for such time differences by temporally realigning the individual slices to a reference section to correct for any phase shifts, to model the signal from the whole volume at the same time point.49 The task force recommends STC at a TR of >2 seconds for both SBC and ICA. If the recommended TR parameter is followed at a TR of ≤2, then STC would be an optional step.

At a TR of ≤2 seconds, STC will likely have minimal benefit in detecting activation in the RSNs compared with not applying the correction.49 At this short TR, acquisition delays between slices are minimal. The Human Connectome Project rs-fMRI used a subsecond TR and did not use STC because of unavoidable errors from temporal interpolation that could obscure high-frequency signals.22 Parker et al24 have shown that STC at a TR of <2 seconds for tb-fMRI TRs of 0.5 and 1.1 seconds using FSL and SPM resulted in only minimal benefits of 2.2% and 5% compared with uncorrected data at TR = 2 seconds for which the benefit was 15.6%.24 Poldrack et al50 do not recommend using STC at a short TR because artifacts in the reference image could be propagated to other slices.

At a longer TR, STC can improve detection of both rs-FC and tb-fMRI activations by removing temporal sources of variance,22 particularly in cases with medium-to-high motion.49 Parker et al24 demonstrated a improvement of 55.7% in global t-statistics at a TR of 5 seconds compared with or without STC. STC is especially important when mapping the dorsal areas such as the motor cortex.48 STC at a TR of >2 can also be synergistic when combined with other preprocessing steps. Because movement introduces both spatial and temporal artifacts, a combination of STC and motion correction is needed to avoid the time-series consisting of temporally nonuniform samples.48 Additionally, STC is necessary when using spatial smoothing because slices with large delays could introduce residual data when averaged with adjacent slices with smaller delays.24

From our literature review, 62/86 (72%) studies performed STC, among which 26 studies were scanned at a TR of ≤2 seconds and the other 36 were scanned at TR >2 seconds.

Elimination of Systematic Odd-Even Section-Intensity Differences: Optional.

During interleaved section acquisition, odd-numbered and even-numbered slices are acquired with a relatively large time difference, which can be up to half the TR. The task force considers elimination of systematic odd-even section-intensity differences an optional preprocessing step.

On the basis of expert opinion, it is no longer necessary to eliminate odd-even section-intensity differences with newer model scanners. However, before the advent of such scanners, elimination of odd-even section-intensity differences was necessary to exclude crosstalk between interleaved section acquisitions.51 Additionally, limited studies and rs-fMRI software tools use this preprocessing step.

From our literature review, 11/86 studies (13%) eliminated systematic odd-even section-intensity differences.

Despiking: Recommended for SBC Only.

Despiking is a method to correct spikes representing artifacts induced by sudden motion or system instability in the fMRI time-series by truncating,40 removing, or interpolating52 signal of the independent voxels. Spikes are often defined as signals that exceed the median and/or mean of the rs-fMRI time-series by a set SD. The task force would recommend despiking for SBC only. On the basis of the literature, a maximum threshold of <5% would likely be acceptable. Patel et al52 reported wavelet despiking at an average of 1.5% and excluded patients with spike percentages of >5% because they had moved excessively. Power et al53 also used the despiking setting of 4% with the ArtRepair software (https://www.nitrc.org/projects/art_repair/).

Despiking can identify and remove a wide range of movement-induced artifacts across different frequencies that may not be typically removed by other preprocessing techniques, such as linear regression.52 Even small movements of the head can introduce secondary sources of artifacts, including spin-history artifacts, which have failed to be effectively removed by nuisance regression and/or volume censoring.52 However, despiking, specifically wavelet despiking, recently introduced by Patel et al52 has proved effective in removing these types of motion artifacts from low-to-high frequencies. Patel et al showed that combining wavelet despiking with regression was superior in removing both linear and nonlinear sources of artifacts related to movement and retained less signal variance compared with nuisance regression alone. When combined with nuisance regression, it could identify correlation estimates at strengths similar to those of volume censoring.40 However, compared with volume censoring, despiking removes voxels with motion artifacts without removing the entire volume of data.52 Despiking is especially recommended in patients with potentially rapid head movements, such as patients with epilepsy and/or pediatric patients.52

On the other hand, despiking can potentially flag too many data points for correction. Replacing flagged data by interpolating adjacent data could add too many artificial signals. Removing too many data points could prohibit detection of functional correlations. Therefore, when using despiking, users need to avoid being too aggressive.

From our literature review, only 8/86 studies (9.3%) used despiking, because it is not available in many commonly used software packages. However, among the 8 studies that used it, 14% of the studies that employed SBC used despiking, whereas 5% of the studies that utilized ICA used despiking.

Volume Censoring/Scrubbing: Recommended for Both SBC and ICA.

Volume censoring or scrubbing is frame wise removal of any volume with excessive movement or signal changes over a predetermined threshold.41 Such volumes are identified by first calculating the frame wise displacement of the head position, which measures how much the head moved compared with previous time points and/or DVARS (D: temporal derivative of time courses, VARS: RMS variance over voxels), which measures the rate of change of BOLD signal across the entire brain at each frame of data.41 If the frame wise displacement or DVARS of specific volume exceeds a set threshold, that volume would be either dampened, removed,41 or interpolated.27 The task force would recommend volume censoring for both SBC and ICA.

The threshold will determine how much data will be removed. It will depend on various factors, such as the number of time points and the duration of the scan. The task force cannot recommend a specific threshold at this time. On the basis of the literature, Power et al41 chose a value of 0.5 mm for frame wise displacement and a 0.5% change in BOLD signal for DVARS to represent the minimum threshold for movement in still adults. In healthy children, they reported approximately 25% of the rs-fMRI data being affected by motion artifacts. They required a minimum of at least 125 frames, around 5 minutes of data, to be kept after scrubbing, but they had no maximum threshold for how much data could be removed.41

Artifacts in rs-fMRI data can be caused by various sources.41 Susceptibility artifacts can cause image distortions and signal dropouts.41 Even a small head movement can cause a shift in the position of the brain in space, which can cause a large difference in the amplitude of the BOLD signal and subsequently changes in rs-FC.41 Head movement can also cause short-range correlations to strengthen, whereas medium- to long-distance FC weakens them.40 Volume censoring can correct for this bias.40 Although volume censoring and despiking have similar goals in eliminating motion artifacts exceeding a threshold, volume censoring may be advantageous in patients with the potential for large movements,3 removing entire frames of data instead of only affected voxels. Additionally, when slow, residual movements are spread over consecutive voxels, volume censoring may, in theory, perform better than despiking.

The disadvantage with volume censoring is that because entire frames of data are removed, more data are typically removed than in other preprocessing steps. Power et al41 reported removing up to 39% of the data after volume censoring of 22 healthy children who underwent rs-fMRI. For cooperative patients with relatively little motion, volume censoring is expected to be beneficial; however, in patients who move excessively, volume censoring may be unfavorable.

From our literature review, 20/86 (23%) studies performed volume censoring.

Linear Detrending: Optional.

Linear detrending removes linear BOLD signal drifts or trends typically caused by scanner instability, physiologic fluctuations, and/or head motion.54,55 The task force considers linear detrending optional.

Typically, linear signal drifts are low-frequency in nature and can mostly be accounted for by using bandpass and/or high-pass filtering. However, if temporal filtering is not performed, linear detrending is necessary and can help account for scanner instabilities or residual slow head movement.

From our literature review, 41/86 (48%) studies performed linear detrending.

Nuisance Regression: CSF/White Matter Regression—Recommended for SBC Only.

Nuisance signal regression removes temporal components in BOLD signal time courses that are correlated with head motion and CSF/white matter signal fluctuations to eliminate non-neural contributions.29 Currently, the main method for nuisance signal regression is a general linear model–based approach in which motion time curves and tissue-based signal time courses are regressed from the rs-fMRI data.56 The task force would recommend nuisance regression of CSF/white matter signal time curves for SBC only.

Because most neuronal activation occurs in the gray matter, signal changes in the white matter and CSF would mostly be non-neural in origin, such as cardiac and respiratory fluctuations.29 These can be estimated from various sources including anatomic data, ROIs with high temporal SDs, and noise components from ICA or principal component analysis.29,57 Nuisance regression of CSF, white matter, and head motion can reduce temporal SDs29 and improve the specificity at which FC can be estimated.56 Muschelli et al56 noted a decrease of motion artifacts, causing variability in FC while preserving the signal of interest with nuisance regression of CSF and white matter. While bandpass filtering without nuisance regression reduces BOLD signal fluctuations due to motion, it did not prevent the spread of motion-contaminated BOLD signal fluctuations.58

In cases of standard space transformation for individual patients, incorrect tissue segmentation or inclusion of nuisance signals that represent neural activity would reduce the performance of nuisance regression.29 Furthermore, a portion of white matter or CSF can be misclassified by large brain tumors or other lesions, affecting the fidelity of the nuisance regressors. From our literature review, 51/86 (59%) studies performed nuisance regression of CSF and/or white matter. Forty-eight of 51 (94%) of these performed both white matter and CSF regression, while 3/51 (5.9%) performed regression for only CSF. Of these 51 studies, 79% of the studies used SBC compared with 33% of the studies that used ICA.

Nuisance Regression: Head Motion Regression—Recommended for Both SBC and ICA.

Head motion regression is another type of nuisance regression in which translational and rotational motion estimates from image realignment are applied as the nuisance regressors.27 The number of motion parameters ranges from 6 to 36,27,59 with 6 being the most common.27 The expert task force recommends head motion regression for both SBC and ICA.

Due to the complex effects of head motion, image spatial realignment is not enough to fully eliminate motion artifacts,56 and additional correction is of benefit. Although volume registration works well for small movements, larger motion errors can arise during realignment.3 Patients may move more than healthy adults.3 Furthermore, head movement can warp the magnetization gradient,3 possibly resulting in image distortions.

A possible problem with head motion regression is that in cases of extensive head motion, the realignment parameters may still not fully explain the motion-related signal changes.27 Additionally, an excess of motion regressors could remove neuronal-related signal fluctuations,27 especially in cases in which there is minimal head movement.3 From our literature review, 45/86 (52%) studies conducted head motion regression.

Nuisance Regression: Global Signal Regression Optional.

Global signal regression (GSR) is regressing out the average time-series across the whole-brain volume. GSR is an effective though controversial means of reducing widely shared variance and thereby improving the spatial specificity of computed maps.60⇓-62 The task force considers GSR an optional preprocessing step.

Part of the global signal is of neural origin;63 however, much of the global signal represents non-neural artifacts attributable to physical effects of head motion31,59,64,65 and variations in the partial pressure of arterial carbon dioxide.66 GSR can reduce signal variances due to head motion and physiologic fluctuations better than CSF and white matter regression and motion correction combined.31 Without GSR, all parts of the brain appear to be strongly positively correlated.67⇓⇓-70 GSR causes all subsequently computed correlation maps to be approximately zero-centered; in other words, positive and negative values are approximately balanced over the whole brain.60 Thus, GSR negatively biases all computed correlations but preserves relative iso-correlation contours. This negative bias has caused some to criticize GSR because it induces artifactual anticorrelations71,72 and removes neural components in the global signal, though an alternative counter view is that widely shared variance in the fMRI signal induces artifactual positive correlations. More recent objections to GSR suggest that it can distort quantitative FC differences across diagnostic groups.73,74 A more recent consensus article attempts to reconcile these opposing viewpoints.75

From our literature review, 27/86 (31%) studies conducted GSR.

Temporal Filtering: Recommended Bandpass Filtering for Both SBC and ICA.

Bandpass, low-pass, or high-pass temporal filtering has been commonly applied for rs-fMRI. This preprocessing step removes BOLD signal components with frequencies typically lower than 0.01 Hz and/or higher than 0.1 Hz. The task force recommends bandpass filtering the rs-fMRI data for both SBC and ICA. On the basis of the literature, 0.01–0.08 Hz was the most common bandpass filtering frequency range.

Filtering out any frequencies outside the typical rs-fMRI frequency range of 0.01–0.1 Hz is important to eliminate any residual noise from head motion, physiologic origins, and/or low-frequency drifts.76 Bandpass filtering increased the signal-to-noise separation within well-known RSNs and increased the test-retest reliability of whole-brain connectivity in both healthy controls and subjects with mild Alzheimer disease.77 Bandpass filtering is often combined with nuisance regression of CSF/WM, motion, and global signal.58 In a study conducted by Risk et al,78 the accumulation of spatially heterogeneous multiband noise, the physiologic noise from CSF pulsations, and the variance from intracranial brain motion increased the SD and resulted in reduced rs-FC estimates, even when using nuisance regression. However, when nuisance regression was combined with bandpass filtering, they obtained higher functional correlations at higher multiband factors.78 Additionally, Van Dijk et al79 demonstrated that linear trends were removed with bandpass filtering, while maintaining frequencies of <0.08 Hz. Overall, bandpass filtering allows removal of extremes of high and low BOLD signal frequencies and would, therefore, allow the best estimate of localization of RSNs. The upper and lower thresholds at which the BOLD signal is filtered usually depend on the institution.

A disadvantage of bandpass filtering is that neural signal above or below the thresholds could be lost.78 Physiologic fluctuations in BOLD signal existing from 0.01 to 0.1 Hz may still not be removed with bandpass filtering. For example, low-frequency fluctuations due to the heart rate can occur at 0.04 Hz, and small fluctuations in breathing, at 0.03 Hz.27 While such physiologic fluctuations are non-neural in nature,27 they will be reflected in the BOLD signal in white matter and CSF, which can be removed through nuisance regression.

Low-pass and high-pass filtering can also be used in rs-fMRI preprocessing. Low-pass filtering is advantageous because it can filter out non-neural signals that are typically above 0.1 Hz.27 Because most physiologic noise typically presents at high frequencies,29 low-pass filtering can effectively remove such sources of noise while retaining the rs-BOLD signal of interest. However, intrinsic brain signal could still exist beyond 0.1 Hz.27 Studies that used high-pass filtering detected only frequencies above, usually, 0.01 Hz, because any frequencies below 0.01 Hz most likely do not represent true rs-fMRI signal but represent noise instead. High-pass filtering can be used as an alternative to linear detrending because it can remove linear drifts that occur at low frequencies, below 0.02 Hz. However, high-pass filtering cannot remove motion artifacts at frequencies above 0.01 Hz.

From our literature review, 75/86 (87%) studies applied a temporal filter to the rs-fMRI data. Forty-five of 75 (60%) studies applied bandpass filtering, 20/75 (27%) studies applied low-pass filtering, and 10/75 (13%) studies applied high-pass filtering.

Spatial Smoothing: Recommended with a Kernel Size Twice the Voxel Size for Both SBC and ICA.

For spatial smoothing, the signal at each voxel is averaged across a range of neighboring voxels to reduce noise80 and increases sensitivity.81 The task force recommends spatial smoothing for both SBC and ICA with a kernel size approximately twice the acquired voxel size. Kokkonen et al82 reported unsuccessful mapping of sensorimotor areas when using unsmoothed data. Huang et al83 reported that a Gaussian kernel size of 6-mm full width at half maximum with approximately 3-mm isotropic voxels increased the SNR of BOLD to enable more reliable mapping of motor and language areas. Alakorkko et al80 showed that spatial smoothing can increase the correlation strength of voxels across rs-FCs. With young children with smaller brain sizes, the operator could consider proportionally reducing the voxel size and number of slices.

A smoothing kernel that is too small may have little benefit, while a kernel that is too large could reduce spatial specificity.81 A kernel size that is twice the voxel size of the functional images has been recommended84⇓-86 to ensure the validity of the random field theory–based multiple comparison correction.86

From our literature review, 78/86 (91%) studies performed spatial smoothing. The kernel size ranged from 1 to 10 mm full width at half maximum, with a mean, mode, and median of 6.1, 6, and 6 mm full width at half maximum, respectively. Seventy-four of 78 (95%) studies reported the kernel size they used. Thirty-eight of 74 (51%) studies used a kernel size that was twice the voxel size.

CONCLUSIONS

The American Society of Functional Neuroradiology, the American Society of Pediatric Neuroradiology, and the American Society of Neuroradiology Clinical Translation of Functional and Diffusion MR Imaging Study Group suggests the use of the proposed standardized rs-fMRI acquisition and preprocessing steps as initial guidelines for institutions using rs-fMRI for preoperative mapping of language, motor, and visual areas in patients with brain tumors and epilepsy. The recommendations provided are based on a comprehensive review of the literature and consensus opinion from experts in fMRI from institutions in the United States and Canada. These rs-fMRI guidelines may lead to the development of a standard rs-fMRI pipeline as well as commercial rs-fMRI processing software. The rs-fMRI guidelines will also encourage and standardize multicenter studies that will help validate rs-fMRI for widespread clinical use. Future studies are needed to define a specific order of the rs-fMRI preprocessing steps, because currently, there is insufficient literature support and not enough expert consensus to provide an order for all the steps. Further studies are also needed evaluating the interactions of different preprocessing steps based on their order of implementation. Finally, the task force would emphasize that while the recommended acquisition/preprocessing steps are preferred, the ones that were deemed optional are not necessarily precluded and may be beneficial depending on the circumstances.

Footnotes

  • From the American Society of Functional Neuroradiology (ASFNR), American Society of Pediatric Neuroradiology (ASPNR), American Society of Neuroradiology (ASNR) Clinical Translation of Functional and Diffusion MRI Study Group.

  • V.A. Kumar and J. Lee are co-first authors.

  • Disclosure forms provided by the authors are available with the full text and PDF of this article at www.ajnr.org.

References

  1. 1.↵
    1. Leuthardt EC,
    2. Guzman G,
    3. Bandt SK, et al
    . Integration of resting state functional MRI into clinical practice: a large single institution experience. PLoS One 2018;13:e0198349 doi:10.1371/journal.pone.0198349 pmid:29933375
    CrossRefPubMed
  2. 2.↵
    1. Kumar VA,
    2. Heiba IM,
    3. Prabhu SS, et al
    . The role of resting-state functional MRI for clinical preoperative language mapping. Cancer Imaging 2020;20:47 doi:10.1186/s40644-020-00327-w pmid:32653026
    CrossRefPubMed
  3. 3.↵
    1. Maknojia S,
    2. Churchill NW,
    3. Schweizer TA, et al
    . Resting state fMRI: going through the motions. Front Neurosci 2019;13:825 doi:10.3389/fnins.2019.00825 pmid:31456656
    CrossRefPubMed
  4. 4.↵
    1. Huijbers W,
    2. Van Dijk KR,
    3. Boenniger MM, et al
    . Less head motion during MRI under task than resting-state conditions. Neuroimage 2017;147:111–20 doi:10.1016/j.neuroimage.2016.12.002 pmid:27919751
    CrossRefPubMed
  5. 5.↵
    1. Black DF,
    2. Vachha B,
    3. Mian A, et al
    . American Society of Functional Neuroradiology-recommended fMRI paradigm algorithms for presurgical language assessment. AJNR Am J Neuroradiol 2017;38:E65–73 doi:10.3174/ajnr.A5345 pmid:28860215
    Abstract/FREE Full Text
  6. 6.↵
    1. Niederberger M,
    2. Spranger J
    . Delphi technique in health sciences: a map. Front Public Health 2020;8:457 doi:10.3389/fpubh.2020.00457 pmid:33072683
    CrossRefPubMed
  7. 7.↵
    1. Birn RM,
    2. Molloy EK,
    3. Patriat R, et al
    . The effect of scan length on the reliability of resting-state fMRI connectivity estimates. Neuroimage 2013;83:550–58 doi:10.1016/j.neuroimage.2013.05.099 pmid:23747458
    CrossRefPubMed
  8. 8.↵
    1. Abdul Wahab NS,
    2. Yahya N,
    3. Yusoff AN, et al
    . Effects of different scan duration on brain effective connectivity among default mode network nodes. Diagnostics (Basel) 2022;12:12 doi:10.3390/diagnostics12051277 pmid:35626432
    CrossRefPubMed
  9. 9.↵
    1. Van Dijk KR,
    2. Hedden T,
    3. Venkataraman A, et al
    . Intrinsic functional connectivity as a tool for human connectomics: theory, properties, and optimization. J Neurophysiol 2010;103:297–321 doi:10.1152/jn.00783.2009 pmid:19889849
    CrossRefPubMed
  10. 10.↵
    1. Vakamudi K,
    2. Posse S,
    3. Jung R, et al
    . Real-time presurgical resting-state fMRI in patients with brain tumors: quality control and comparison with task-fMRI and intraoperative mapping. Hum Brain Mapp 2020;41:797–814 doi:10.1002/hbm.24840 pmid:31692177
    CrossRefPubMed
  11. 11.↵
    1. Patriat R,
    2. Molloy EK,
    3. Meier TB, et al
    . The effect of resting condition on resting-state fMRI reliability and consistency: a comparison between resting with eyes open, closed, and fixated. Neuroimage 2013;78:463–73 doi:10.1016/j.neuroimage.2013.04.013 pmid:23597935
    CrossRefPubMed
  12. 12.↵
    1. Allen EA,
    2. Damaraju E,
    3. Eichele T, et al
    . EEG signatures of dynamic functional network connectivity states. Brain Topogr 2018;31:101–16 doi:10.1007/s10548-017-0546-2 pmid:28229308
    CrossRefPubMed
  13. 13.↵
    1. Tagliazucchi E,
    2. Laufs H
    . Decoding wakefulness levels from typical fMRI resting-state data reveals reliable drifts between wakefulness and sleep. Neuron 2014;82:695–708 doi:10.1016/j.neuron.2014.03.020 pmid:24811386
    CrossRefPubMed
  14. 14.↵
    1. Wang J,
    2. Han J,
    3. Nguyen VT, et al
    . Improving the test-retest reliability of resting state fMRI by removing the impact of sleep. Front Neurosci 2017;11:249 doi:10.3389/fnins.2017.00249 pmid:28533739
    CrossRefPubMed
  15. 15.↵
    1. Agcaoglu O,
    2. Wilson TW,
    3. Wang YP, et al
    . Resting state connectivity differences in eyes open versus eyes closed conditions. Hum Brain Mapp 2019;40:2488–98 doi:10.1002/hbm.24539 pmid:30720907
    CrossRefPubMed
  16. 16.↵
    1. Zou Q,
    2. Miao X,
    3. Liu D, et al
    . Reliability comparison of spontaneous brain activities between BOLD and CBF contrasts in eyes-open and eyes-closed resting states. Neuroimage 2015;121:91–10 doi:10.1016/j.neuroimage.2015.07.044 pmid:26226087
    CrossRefPubMed
  17. 17.↵
    1. Costumero V,
    2. Bueichekú E,
    3. Adrián-Ventura J, et al
    . Opening or closing eyes at rest modulates the functional connectivity of V1 with default and salience networks. Sci Rep 2020;10:9137 doi:10.1038/s41598-020-66100-y pmid:32499585
    CrossRefPubMed
  18. 18.↵
    1. Wei J,
    2. Chen T,
    3. Li C, et al
    . Eyes-open and eyes-closed resting states with opposite brain activity in sensorimotor and occipital regions: multidimensional evidences from machine learning perspective. Front Hum Neurosci 2018;12:422 doi:10.3389/fnhum.2018.00422 pmid:30405376
    CrossRefPubMed
  19. 19.↵
    1. Wang Z,
    2. Liu J,
    3. Zhong N, et al
    . Changes in the brain intrinsic organization in both on-task state and post-task resting state. Neuroimage 2012;62:394–407 doi:10.1016/j.neuroimage.2012.04.051 pmid:22569542
    CrossRefPubMed
  20. 20.↵
    1. Tung KC,
    2. Uh J,
    3. Mao D, et al
    . Alterations in resting functional connectivity due to recent motor task. Neuroimage 2013;78:316–24 doi:10.1016/j.neuroimage.2013.04.006 pmid:23583747
    CrossRefPubMed
  21. 21.↵
    1. Feinberg DA,
    2. Moeller S,
    3. Smith SM, et al
    . Multiplexed echo planar imaging for sub-second whole brain FMRI and fast diffusion imaging. PLoS One 2010;5:e15710 doi:10.1371/journal.pone.0015710 pmid:21187930
    CrossRefPubMed
  22. 22.↵
    1. Smith SM,
    2. Beckmann CF,
    3. Andersson J, et al
    ; WU-Minn HCP Consortium. Resting-state fMRI in the Human Connectome Project. Neuroimage 2013;80:144–68 doi:10.1016/j.neuroimage.2013.05.039 pmid:23702415
    CrossRefPubMed
  23. 23.↵
    1. Voets NL,
    2. Plaha P,
    3. Parker Jones O, et al
    . Presurgical localization of the primary sensorimotor cortex in gliomas: when is resting state FMRI beneficial and sufficient? Clin Neuroradiol 2021;31:245–56 doi:10.1007/s00062-020-00879-1 pmid:32274518
    CrossRefPubMed
  24. 24.↵
    1. Parker D,
    2. Liu X,
    3. Razlighi QR
    . Optimal slice timing correction and its interaction with fMRI parameters and artifacts. Med Image Anal 2017;35:434–45 doi:10.1016/j.media.2016.08.006 pmid:27589578
    CrossRefPubMed
  25. 25.↵
    1. Birn RM,
    2. Diamond JB,
    3. Smith MA, et al
    . Separating respiratory-variation-related fluctuations from neuronal-activity-related fluctuations in fMRI. Neuroimage 2006;31:1536–48 doi:10.1016/j.neuroimage.2006.02.048 pmid:16632379
    CrossRefPubMed
  26. 26.↵
    1. Lin FH,
    2. Nummenmaa A,
    3. Witzel T, et al
    . Physiological noise reduction using volumetric functional magnetic resonance inverse imaging. Hum Brain Mapp 2012;33:2815–30 doi:10.1002/hbm.21403 pmid:21954026
    CrossRefPubMed
  27. 27.↵
    1. Caballero-Gaudes C,
    2. Reynolds RC
    . Methods for cleaning the BOLD fMRI signal. Neuroimage 2017;154:128–49 doi:10.1016/j.neuroimage.2016.12.018 pmid:27956209
    CrossRefPubMed
  28. 28.↵
    1. Glover GH,
    2. Li TQ,
    3. Ress D
    . Image-based method for retrospective correction of physiological motion effects in fMRI: RETROICOR. Magn Reson Med 2000;44:162–67 doi:10.1002/1522-2594(200007)44:1<162::AID-MRM23>3.0.CO;2-E pmid:10893535
    CrossRefPubMed
  29. 29.↵
    1. Behzadi Y,
    2. Restom K,
    3. Liau J, et al
    . A component based noise correction method (CompCor) for BOLD and perfusion based fMRI. Neuroimage 2007;37:90–101 doi:10.1016/j.neuroimage.2007.04.042 pmid:17560126
    CrossRefPubMed
  30. 30.↵
    1. Golestani AM,
    2. Chen JJ
    . Performance of temporal and spatial independent component analysis in identifying and removing low-frequency physiological and motion effects in resting-state fMRI. Front Neurosci 2022;16:867243 doi:10.3389/fnins.2022.867243 pmid:35757543
    CrossRefPubMed
  31. 31.↵
    1. Power JD,
    2. Plitt M,
    3. Laumann TO, et al
    . Sources and implications of whole-brain fMRI signals in humans. Neuroimage 2017;146:609–25 doi:10.1016/j.neuroimage.2016.09.038 pmid:27751941
    CrossRefPubMed
  32. 32.↵
    1. Frank LR,
    2. Buxton RB,
    3. Wong EC
    . Estimation of respiration-induced noise fluctuations from undersampled multislice fMRI data. Magn Reson Med 2001;45:635–44 doi:10.1002/mrm.1086 pmid:11283992
    CrossRefPubMed
  33. 33.↵
    1. Naganawa S,
    2. Nihashi T,
    3. Fukatsu H, et al
    . Pre-surgical mapping of primary motor cortex by functional MRI at 3 T: effects of intravenous administration of Gd-DTPA. Eur Radiol 2004;14:112–14 doi:10.1007/s00330-003-2147-6 pmid:14600780
    CrossRefPubMed
  34. 34.↵
    1. Vachha B,
    2. Huang SY
    . MRI with ultrahigh field strength and high-performance gradients: challenges and opportunities for clinical neuroimaging at 7 T and beyond. Eur Radiol Exp 2021;5:35 doi:10.1186/s41747-021-00216-2 pmid:34435246
    CrossRefPubMed
  35. 35.↵
    1. Garcia-Eulate R,
    2. Garcia-Garcia D,
    3. Dominguez PD, et al
    . Functional bold MRI: advantages of the 3 T vs. the 1.5 T. Clin Imaging 2011;35:236–41 doi:10.1016/j.clinimag.2010.07.003 pmid:21513865
    CrossRefPubMed
  36. 36.↵
    1. Krasnow B,
    2. Tamm L,
    3. Greicius MD, et al
    . Comparison of fMRI activation at 3 and 1.5 T during perceptual, cognitive, and affective processing. Neuroimage 2003;18:813–26 doi:10.1016/s1053-8119(03)00002-8 pmid:12725758
    CrossRefPubMed
  37. 37.↵
    1. Gorgolewski KJ,
    2. Mendes N,
    3. Wilfling D, et al
    . A high resolution 7-Tesla resting-state fMRI test-retest dataset with cognitive and physiological measures. Sci Data 2015;2:140054 doi:10.1038/sdata.2014.54 pmid:25977805
    CrossRefPubMed
  38. 38.↵
    1. Bianciardi M,
    2. Fukunaga M,
    3. van Gelderen P, et al
    . Sources of functional magnetic resonance imaging signal fluctuations in the human brain at rest: a 7 T study. Magn Reson Imaging 2009;27:1019–29 doi:10.1016/j.mri.2009.02.004 pmid:19375260
    CrossRefPubMed
  39. 39.↵
    1. Jiang A,
    2. Kennedy DN,
    3. Baker JR, et al
    . Motion detection and correction in functional MR imaging. Human Brain Mapping 1995;3:224–35 doi:10.1002/hbm.460030306
    CrossRef
  40. 40.↵
    1. Jo HJ,
    2. Gotts SJ,
    3. Reynolds RC, et al
    . Effective preprocessing procedures virtually eliminate distance-dependent motion artifacts in resting state FMRI. J Appl Math 2013;2013:10.1155/2013/935154 doi:10.1155/2013/935154 pmid:24415902
    CrossRefPubMed
  41. 41.↵
    1. Power JD,
    2. Barnes KA,
    3. Snyder AZ, et al
    . Spurious but systematic correlations in functional connectivity MRI networks arise from subject motion. Neuroimage 2012;59:2142–54 doi:10.1016/j.neuroimage.2011.10.018 pmid:22019881
    CrossRefPubMed
  42. 42.↵
    1. Oakes TR,
    2. Johnstone T,
    3. Ores Walsh KS, et al
    . Comparison of fMRI motion correction software tools. Neuroimage 2005;28:529–43 doi:10.1016/j.neuroimage.2005.05.058 pmid:16099178
    CrossRefPubMed
  43. 43.↵
    1. Beall EB,
    2. Lowe MJ
    . SimPACE: generating simulated motion corrupted BOLD data with synthetic-navigated acquisition or the development and evaluation of SLOMOCO: a new, highly effective slicewise motion correction. Neuroimage 2014;101:21–34 doi:10.1016/j.neuroimage.2014.06.038 pmid:24969568
    CrossRefPubMed
  44. 44.↵
    1. Johnstone T,
    2. Ores Walsh KS,
    3. Greischar LL, et al
    . Motion correction and the use of motion covariates in multiple-subject fMRI analysis. Hum Brain Mapp 2006;27:779–88 doi:10.1002/hbm.20219 pmid:16456818
    CrossRefPubMed
  45. 45.↵
    1. Woods RP,
    2. Cherry SR,
    3. Mazziotta JC
    . Rapid automated algorithm for aligning and reslicing PET images. J Comput Assist Tomogr 1992;16:620–33 doi:10.1097/00004728-199207000-00024 pmid:1629424
    CrossRefPubMed
  46. 46.↵
    1. Woods RP,
    2. Mazziotta JC,
    3. Cherry SR
    . MRI-PET registration with automated algorithm. J Comput Assist Tomogr 1993;17:536–46 doi:10.1097/00004728-199307000-00004 pmid:8331222
    CrossRefPubMed
  47. 47.↵
    1. Friston KJ,
    2. Williams S,
    3. Howard R, et al
    . Movement-related effects in fMRI time-series. Magn Reson Med 1996;35:346–55 doi:10.1002/mrm.1910350312 pmid:8699946
    CrossRefPubMed
  48. 48.↵
    1. Sladky R,
    2. Friston KJ,
    3. Tröstl J, et al
    . Slice-timing effects and their correction in functional MRI. Neuroimage 2011;58:588–94 doi:10.1016/j.neuroimage.2011.06.078 pmid:21757015
    CrossRefPubMed
  49. 49.↵
    1. Parker DB,
    2. Razlighi QR
    . The benefit of slice timing correction in common fMRI preprocessing pipelines. Front Neurosci 2019;13:821 doi:10.3389/fnins.2019.00821 pmid:31551667
    CrossRefPubMed
  50. 50.↵
    1. Poldrack RM,
    2. Mumford JA,
    3. Nichols TE
    . Handbook of Functional MRI Data Analysis. Cambridge University Press; 2011
  51. 51.↵
    1. Simmons A,
    2. Tofts PS,
    3. Barker GJ, et al
    . Sources of intensity nonuniformity in spin echo images at 1.5 T. Magn Reson Med 1994;32:121–28 doi:10.1002/mrm.1910320117 pmid:8084227
    CrossRefPubMed
  52. 52.↵
    1. Patel AX,
    2. Kundu P,
    3. Rubinov M, et al
    . A wavelet method for modeling and despiking motion artifacts from resting-state fMRI time series. Neuroimage 2014;95:287–304 doi:10.1016/j.neuroimage.2014.03.012 pmid:24657353
    CrossRefPubMed
  53. 53.↵
    1. Power JD,
    2. Plitt M,
    3. Kundu P, et al
    . Temporal interpolation alters motion in fMRI scans: Magnitudes and consequences for artifact detection. PLoS One 2017;12:e0182939 doi:10.1371/journal.pone.0182939 pmid:28880888
    CrossRefPubMed
  54. 54.↵
    1. Tanabe J,
    2. Miller D,
    3. Tregellas J, et al
    . Comparison of detrending methods for optimal fMRI preprocessing. Neuroimage 2002;15:902–07 doi:10.1006/nimg.2002.1053 pmid:11906230
    CrossRefPubMed
  55. 55.↵
    1. Kopel R,
    2. Sladky R,
    3. Laub P, et al
    . No time for drifting: comparing performance and applicability of signal detrending algorithms for real-time fMRI. Neuroimage 2019;191:421–29 doi:10.1016/j.neuroimage.2019.02.058 pmid:30818024
    CrossRefPubMed
  56. 56.↵
    1. Muschelli J,
    2. Nebel MB,
    3. Caffo BS, et al
    . Reduction of motion-related artifacts in resting state fMRI using aCompCor. Neuroimage 2014;96:22–35 doi:10.1016/j.neuroimage.2014.03.028 pmid:24657780
    CrossRefPubMed
  57. 57.↵
    1. Middlebrooks EH,
    2. Frost CJ,
    3. Tuna IS, et al
    . Reduction of motion artifacts and noise using independent component analysis in task-based functional MRI for preoperative planning in patients with brain tumor. AJNR Am J Neuroradiol 2017;38:336–42 doi:10.3174/ajnr.A4996 pmid:28056453
    Abstract/FREE Full Text
  58. 58.↵
    1. Hallquist MN,
    2. Hwang K,
    3. Luna B
    . The nuisance of nuisance regression: spectral misspecification in a common approach to resting-state fMRI preprocessing reintroduces noise and obscures functional connectivity. Neuroimage 2013;82:208–25 doi:10.1016/j.neuroimage.2013.05.116 pmid:23747457
    CrossRefPubMed
  59. 59.↵
    1. Power JD,
    2. Mitra A,
    3. Laumann TO, et al
    . Methods to detect, characterize, and remove motion artifact in resting state fMRI. Neuroimage 2014;84:320–41 doi:10.1016/j.neuroimage.2013.08.048 pmid:23994314
    CrossRefPubMed
  60. 60.↵
    1. Fox MD,
    2. Zhang D,
    3. Snyder AZ, et al
    . The global signal and observed anticorrelated resting state brain networks. J Neurophysiol 2009;101:3270–83 doi:10.1152/jn.90777.2008 pmid:19339462
    CrossRefPubMed
  61. 61.
    1. Aguirre GK,
    2. Zarahn E,
    3. D'Esposito M
    . The inferential impact of global signal covariates in functional neuroimaging analyses. Neuroimage 1998;8:302–06 doi:10.1006/nimg.1998.0367 pmid:9758743
    CrossRefPubMed
  62. 62.↵
    1. Macey PM,
    2. Macey KE,
    3. Kumar R, et al
    . A method for removal of global effects from fMRI time series. Neuroimage 2004;22:360–66 doi:10.1016/j.neuroimage.2003.12.042 pmid:15110027
    CrossRefPubMed
  63. 63.↵
    1. Scholvinck ML,
    2. Maier A,
    3. Ye FQ, et al
    . Neural basis of global resting-state fMRI activity. Proc Natl Acad Sci U S A 2010;107:10238–43 doi:10.1073/pnas.0913110107 pmid:20439733
    Abstract/FREE Full Text
  64. 64.↵
    1. Yan CG,
    2. Cheung B,
    3. Kelly C, et al
    . A comprehensive assessment of regional variation in the impact of head micromovements on functional connectomics. Neuroimage 2013;76:183–201 doi:10.1016/j.neuroimage.2013.03.004 pmid:23499792
    CrossRefPubMed
  65. 65.↵
    1. Satterthwaite TD,
    2. Wolf DH,
    3. Loughead J, et al
    . Impact of in-scanner head motion on multiple measures of functional connectivity: relevance for studies of neurodevelopment in youth. Neuroimage 2012;60:623–32 doi:10.1016/j.neuroimage.2011.12.063 pmid:22233733
    CrossRefPubMed
  66. 66.↵
    1. Power JD,
    2. Plitt M,
    3. Gotts SJ, et al
    . Ridding fMRI data of motion-related influences: Removal of signals with distinct spatial and physical bases in multiecho data. Proc Natl Acad Sci U S A 2018;115:E2105–14 doi:10.1073/pnas.1720985115 pmid:29440410
    Abstract/FREE Full Text
  67. 67.↵
    1. Lowe MJ,
    2. Mock BJ,
    3. Sorenson JA
    . Functional connectivity in single and multislice echoplanar imaging using resting-state fluctuations. Neuroimage 1998;7:119–32 doi:10.1006/nimg.1997.0315 pmid:9558644
    CrossRefPubMed
  68. 68.↵
    1. Vincent JL,
    2. Snyder AZ,
    3. Fox MD, et al
    . Coherent spontaneous activity identifies a hippocampal-parietal memory network. J Neurophysiol 2006;96:3517–31 doi:10.1152/jn.00048.2006 pmid:16899645
    CrossRefPubMed
  69. 69.↵
    1. Joel SE,
    2. Caffo BS,
    3. van Zijl PC, et al
    . On the relationship between seed-based and ICA-based measures of functional connectivity. Magn Reson Med 2011;66:644–57 doi:10.1002/mrm.22818 pmid:21394769
    CrossRefPubMed
  70. 70.↵
    1. Chai XJ,
    2. Castañón AN,
    3. Ongür D, et al
    . Anticorrelations in resting state networks without global signal regression. Neuroimage 2012;59:1420–28 doi:10.1016/j.neuroimage.2011.08.048 pmid:21889994
    CrossRefPubMed
  71. 71.↵
    1. Anderson JS,
    2. Druzgal TJ,
    3. Lopez-Larson M, et al
    . Network anticorrelations, global regression, and phase-shifted soft tissue correction. Hum Brain Mapp 2011;32:919–34 doi:10.1002/hbm.21079 pmid:20533557
    CrossRefPubMed
  72. 72.↵
    1. Murphy K,
    2. Birn RM,
    3. Handwerker DA, et al
    . The impact of global signal regression on resting state correlations: are anti-correlated networks introduced? Neuroimage 2009;44:893–905 doi:10.1016/j.neuroimage.2008.09.036 pmid:18976716
    CrossRefPubMed
  73. 73.↵
    1. Gotts SJ,
    2. Saad ZS,
    3. Jo HJ, et al
    . The perils of global signal regression for group comparisons: a case study of autism spectrum disorders. Front Hum Neurosci 2013;7:356 doi:10.3389/fnhum.2013.00356 pmid:23874279
    CrossRefPubMed
  74. 74.↵
    1. Hahamy A,
    2. Calhoun V,
    3. Pearlson G, et al
    . Save the global: global signal connectivity as a tool for studying clinical populations with functional magnetic resonance imaging. Brain Connect 2014;4:395–403 doi:10.1089/brain.2014.0244 pmid:24923194
    CrossRefPubMed
  75. 75.↵
    1. Murphy K,
    2. Fox MD
    . Towards a consensus regarding global signal regression for resting state functional connectivity MRI. Neuroimage 2017;154:169–73 doi:10.1016/j.neuroimage.2016.11.052 pmid:27888059
    CrossRefPubMed
  76. 76.↵
    1. Wee CY,
    2. Yap PT,
    3. Denny K, et al
    . Resting-state multi-spectrum functional connectivity networks for identification of MCI patients. PLoS One 2012;7:e37828 doi:10.1371/journal.pone.0037828 pmid:22666397
    CrossRefPubMed
  77. 77.↵
    1. Shirer WR,
    2. Jiang H,
    3. Price CM, et al
    . Optimization of rs-fMRI pre-processing for enhanced signal-noise separation, test-retest reliability, and group discrimination. Neuroimage 2015;117:67–79 doi:10.1016/j.neuroimage.2015.05.015 pmid:25987368
    CrossRefPubMed
  78. 78.↵
    1. Risk BB,
    2. Murden RJ,
    3. Wu J, et al
    . Which multiband factor should you choose for your resting-state fMRI study? Neuroimage 2021;234:117965 doi:10.1016/j.neuroimage.2021.117965 pmid:33744454
    CrossRefPubMed
  79. 79.↵
    1. Van Dijk KR,
    2. Sabuncu MR,
    3. Buckner RL
    . The influence of head motion on intrinsic functional connectivity MRI. Neuroimage 2012;59:431–38 doi:10.1016/j.neuroimage.2011.07.044 pmid:21810475
    CrossRefPubMed
  80. 80.↵
    1. Alakorkko T,
    2. Saarimaki H,
    3. Glerean E, et al
    . Effects of spatial smoothing on functional brain networks. Eur J Neurosci 2017;46:2471–80 doi:10.1111/ejn.13717 pmid:28922510
    CrossRefPubMed
  81. 81.↵
    1. Mikl M,
    2. Marecek R,
    3. Hlustik P, et al
    . Effects of spatial smoothing on fMRI group inferences. Magn Reson Imaging 2008;26:490–503 doi:10.1016/j.mri.2007.08.006 pmid:18060720
    CrossRefPubMed
  82. 82.↵
    1. Kokkonen SM,
    2. Nikkinen J,
    3. Remes J, et al
    . Preoperative localization of the sensorimotor area using independent component analysis of resting-state fMRI. Magn Reson Imaging 2009;27:733–40 doi:10.1016/j.mri.2008.11.002 pmid:19110394
    CrossRefPubMed
  83. 83.↵
    1. Huang H,
    2. Ding Z,
    3. Mao D, et al
    . PreSurgMapp: a MATLAB Toolbox for presurgical mapping of eloquent functional areas based on task-related and resting-state functional MRI. Neuroinformatics 2016;14:421–38 doi:10.1007/s12021-016-9304-y pmid:27221107
    CrossRefPubMed
  84. 84.↵
    1. Friston KJ,
    2. Holmes AP,
    3. Poline JB, et al
    . Analysis of fMRI time-series revisited. Neuroimage 1995;2:45–53 doi:10.1006/nimg.1995.1007 pmid:9343589
    CrossRefPubMed
  85. 85.↵
    1. Ball T,
    2. Breckel TP,
    3. Mutschler I, et al
    . Variability of fMRI-response patterns at different spatial observation scales. Hum Brain Mapp 2012;33:1155–71 doi:10.1002/hbm.21274 pmid:21404370
    CrossRefPubMed
  86. 86.↵
    1. Pajula J,
    2. Tohka J
    . Effects of spatial smoothing on inter-subject correlation based analysis of FMRI. Magn Reson Imaging 2014;32:1114–24 doi:10.1016/j.mri.2014.06.001 pmid:24970023
    CrossRefPubMed
  • Received July 23, 2023.
  • Accepted after revision October 12, 2023.
  • © 2024 by American Journal of Neuroradiology
PreviousNext
Back to top

In this issue

American Journal of Neuroradiology: 45 (2)
American Journal of Neuroradiology
Vol. 45, Issue 2
1 Feb 2024
  • Table of Contents
  • Index by author
  • Complete Issue (PDF)
Advertisement
Print
Download PDF
Email Article

Thank you for your interest in spreading the word on American Journal of Neuroradiology.

NOTE: We only request your email address so that the person you are recommending the page to knows that you wanted them to see it, and that it is not junk mail. We do not capture any email address.

Enter multiple addresses on separate lines or separate them with commas.
Recommended Resting-State fMRI Acquisition and Preprocessing Steps for Preoperative Mapping of Language and Motor and Visual Areas in Adult and Pediatric Patients with Brain Tumors and Epilepsy
(Your Name) has sent you a message from American Journal of Neuroradiology
(Your Name) thought you would like to see the American Journal of Neuroradiology web site.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Cite this article
V.A. Kumar, J. Lee, H.-L. Liu, J.W. Allen, C.G. Filippi, A.I. Holodny, K. Hsu, R. Jain, M.P. McAndrews, K.K. Peck, G. Shah, J.S. Shimony, S. Singh, M. Zeineh, J. Tanabe, B. Vachha, A. Vossough, K. Welker, C. Whitlow, M. Wintermark, G. Zaharchuk, H.I. Sair
Recommended Resting-State fMRI Acquisition and Preprocessing Steps for Preoperative Mapping of Language and Motor and Visual Areas in Adult and Pediatric Patients with Brain Tumors and Epilepsy
American Journal of Neuroradiology Feb 2024, 45 (2) 139-148; DOI: 10.3174/ajnr.A8067

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
0 Responses
Respond to this article
Share
Bookmark this article
Resting-State fMRI in Tumors and Epilepsy
V.A. Kumar, J. Lee, H.-L. Liu, J.W. Allen, C.G. Filippi, A.I. Holodny, K. Hsu, R. Jain, M.P. McAndrews, K.K. Peck, G. Shah, J.S. Shimony, S. Singh, M. Zeineh, J. Tanabe, B. Vachha, A. Vossough, K. Welker, C. Whitlow, M. Wintermark, G. Zaharchuk, H.I. Sair
American Journal of Neuroradiology Feb 2024, 45 (2) 139-148; DOI: 10.3174/ajnr.A8067
del.icio.us logo Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One
Purchase

Jump to section

  • Article
    • Abstract
    • ABBREVIATIONS:
    • LITERATURE SEARCH STRATEGY AND REVIEW PROCESS
    • RECOMMENDATIONS OF ACQUISITION AND PREPROCESSING STEPS
    • CONCLUSIONS
    • Footnotes
    • References
  • Figures & Data
  • Info & Metrics
  • Responses
  • References
  • PDF

Related Articles

  • No related articles found.
  • PubMed
  • Google Scholar

Cited By...

  • Pseudo-Resting-State Functional MRI Derived from Dynamic Susceptibility Contrast Perfusion MRI Can Predict Cognitive Impairment in Glioma
  • Crossref (6)
  • Google Scholar

This article has been cited by the following articles in journals that are participating in Crossref Cited-by Linking.

  • Resting-State Functional MRI: Current State, Controversies, Limitations, and Future Directions—AJR Expert Panel Narrative Review
    Behroze A. Vachha, Vinodh A. Kumar, Jay J. Pillai, Joshua Shimony, Jody Tanabe, Haris I. Sair
    American Journal of Roentgenology 2024
  • Consensus recommendations for clinical functional MRI applied to language mapping
    Natalie L. Voets, Manzar Ashtari, Christian F. Beckmann, Christopher F. Benjamin, Tammie Benzinger, Jeffrey R. Binder, Alberto Bizzi, Bruce Bjornson, Edward F. Chang, Linda Douw, Jodie Gawryluk, Karsten Geletneky, Matthew F. Glasser, Sven Haller, Mark Jenkinson, Jorge Jovicich, Eric Leuthardt, Asim Mian, Thomas E. Nichols, Oiwi Parker Jones, Cyril Pernet, Puneet Plaha, Monika Połczyńska-Bletsos, Cathy J. Price, Geert-Jan Rutten, Michael Scheel, Joshua S. Shimony, Joanna Sierpowska, Lynne J. Williams, Ghoufran Talib, Michael Zeineh, Andreas Bartsch, Susan Bookheimer
    Aperture Neuro 2025 5
  • Identifying Inter‐Individual Differences in Cognitive Decline Using the Brain Connectome in Osteoporosis
    Chao Li, Xiaoping Ren, Kechong Zhou, Quan Sun, Ziwei Liao, Tianlun Gong, Yang Wang
    Journal of Magnetic Resonance Imaging 2025
  • Pseudo-Resting-State Functional MRI Derived from Dynamic Susceptibility Contrast Perfusion MRI Can Predict Cognitive Impairment in Glioma
    Nicholas S. Cho, Chencai Wang, Kathleen Van Dyk, Francesco Sanvito, Sonoko Oshima, Jingwen Yao, Albert Lai, Noriko Salamon, Timothy F. Cloughesy, Phioanh L. Nghiemphu, Benjamin M. Ellingson
    American Journal of Neuroradiology 2024 45 10
  • Resting-State Functional MRI in Dyslexia: A Systematic Review
    Bruce Martins, Isabel A. B. Verrone, Mariana M. I. Sakamoto, Mariana Y. Baba, Melissa E. Yvata, Katerina Lukasova, Mariana P. Nucci
    Biomedicines 2025 13 5
  • Seed-based resting-state connectivity as a neurosignature in fibromyalgia and depression: a narrative systematic review
    Betina Franceschini Tocchetto, Andrea Cristiane Janz Moreira, Álvaro de Oliveira Franco, Iraci L. S. Torres, Felipe Fregni, Wolnei Caumo
    Frontiers in Human Neuroscience 2025 19

More in this TOC Section

  • Synthetic MRI based on 3D-QALAS MR Quantification
  • Delta wave MRI
  • Comparing SS-EPI vs SPLICE in Head and Neck Tumors
Show more NEUROIMAGING PHYSICS/FUNCTIONAL NEUROIMAGING/CT AND MRI TECHNOLOGY

Similar Articles

Advertisement

Indexed Content

  • Current Issue
  • Accepted Manuscripts
  • Article Preview
  • Past Issues
  • Editorials
  • Editor's Choice
  • Fellows' Journal Club
  • Letters to the Editor
  • Video Articles

Cases

  • Case Collection
  • Archive - Case of the Week
  • Archive - Case of the Month
  • Archive - Classic Case

More from AJNR

  • Trainee Corner
  • Imaging Protocols
  • MRI Safety Corner

Multimedia

  • AJNR Podcasts
  • AJNR Scantastics

Resources

  • Turnaround Time
  • Submit a Manuscript
  • Submit a Video Article
  • Submit an eLetter to the Editor/Response
  • Manuscript Submission Guidelines
  • Statistical Tips
  • Fast Publishing of Accepted Manuscripts
  • Graphical Abstract Preparation
  • Imaging Protocol Submission
  • Evidence-Based Medicine Level Guide
  • Publishing Checklists
  • Author Policies
  • Become a Reviewer/Academy of Reviewers
  • News and Updates

About Us

  • About AJNR
  • Editorial Board
  • Editorial Board Alumni
  • Alerts
  • Permissions
  • Not an AJNR Subscriber? Join Now
  • Advertise with Us
  • Librarian Resources
  • Feedback
  • Terms and Conditions
  • AJNR Editorial Board Alumni

American Society of Neuroradiology

  • Not an ASNR Member? Join Now

© 2025 by the American Society of Neuroradiology All rights, including for text and data mining, AI training, and similar technologies, are reserved.
Print ISSN: 0195-6108 Online ISSN: 1936-959X

Powered by HighWire