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Research ArticleBrain

Dilated Perivascular Spaces in the Basal Ganglia Are a Biomarker of Small-Vessel Disease in a Very Elderly Population with Dementia

T.P. Hansen, J. Cain, O. Thomas and A. Jackson
American Journal of Neuroradiology May 2015, 36 (5) 893-898; DOI: https://doi.org/10.3174/ajnr.A4237
T.P. Hansen
aFrom the Centre for Imaging Sciences (T.P.H., J.C., A.J.), Wolfson Molecular Imaging Centre, University of Manchester, Greater Manchester, UK
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J. Cain
aFrom the Centre for Imaging Sciences (T.P.H., J.C., A.J.), Wolfson Molecular Imaging Centre, University of Manchester, Greater Manchester, UK
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O. Thomas
bSalford Royal NHS Foundation Trust (O.T.), Salford, UK.
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A. Jackson
aFrom the Centre for Imaging Sciences (T.P.H., J.C., A.J.), Wolfson Molecular Imaging Centre, University of Manchester, Greater Manchester, UK
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  • Fig 1.
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    Fig 1.

    Images show dilated perivascular spaces in the basal ganglia corresponding to PVS-2BG scores of 1–4.

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    Fig 2.

    A, Boxplot shows the Scheltens white matter scores for the 3 subject groups. B, Boxplot shows the PVS-2BG scores for the basal ganglia in the 3 subject groups.

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    Table 1:

    Modified version of Scheltens scoring scheme used in the study

    SubscaleRange of ScoresDefinition of Scores
    1) Periventricular
        Frontal0/1/20 = absent
        Occipital0/1/21 ≤ 5 mm
        Bands on lateral ventricle0/1/22 ≥ 5 and <10 mm
        Subtotal score≤6
    2) Deep white matter
        Frontal0/1/2/3/4/5/6
        Parietal0/1/2/3/4/5/6
        Occipital0/1/2/3/4/5/6
        Temporal0/1/2/3/4/5/60 = none
        Subtotal score0–241 ≤3 mm, n ≤ 5
    3) Basal ganglia2 ≤ 3 mm, n > 5
        Caudate0/1/2/3/4/5/63 = 4–10 mm, n ≤ 5
        Lentiform nucleus0/1/2/3/4/5/64 = 4–10 mm, n > 6
        Thalamus0/1/2/3/4/5/65 ≥ 11 mm, n > 1
        Subtotal score0–186 = confluent
    4) Subtentorial
        Cerebellum0/1/2/3/4/5/6
        Mesencephalon0/1/2/3/4/5/6
        Medulla0/1/2/3/4/5/6
        Pons0/1/2/3/4/5/6
        Subtotal score0–24
    Total score0–72
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    Table 2:

    Demographic and imaging biomarker data for individual diagnostic groupsa

    GroupHealthyADVaD
    No.654739
    Age (yr)78 (5.6)74.1 (8.5)76.9 (7.7)
    Modified Scheltens score12.50 (2.5)13.16 (2.34)22.76 (2.84)
    PVS-15.87 (0.21)6.03 (0.14)6.34 (0.16)
    PVS-2BG2.1 (0.5)2.22 (0.09)2.471 (0.87)
    PVS-2CSOV2.51 (0.13)2.61 (0.10)2.53 (0.15)
    • ↵a Data are mean values (SD).

    • View popup
    Table 3:

    Inter- and intraobserver variation for PVS scoresa

    Modified Scheltens ScorePVS-1PVS-2PVS-2BG
    Interobserver Agreement
        Rater 1 vs 20.820.790.920.91
        Rater 1 vs 30.910.840.890.86
        Rater 2 vs 30.880.820.830.90
    Intraobserver agreement
        Rater 10.820.870.920.90
        Rater 20.860.960.840.86
    • ↵a Data represent weighted Cohen κ statistics. All ratings were very good, except 0.70, which as good.

    • View popup
    Table 4:

    Results of the multinomial linear regression for each of the 4 scenariosa

    ModelHealthy vs DementiaHealthy vs ADHealthy vs VaDAD vs VaD
    Variables entered in the modelPVS-1PVS-1PVS-1PVS-1
    PVS-2BGPVS-2BGPVS-2BGPVS-2BG
    Modified ScheltensModified ScheltensModified ScheltensModified Scheltens
    Variables included in the modelPVS-2BGPVS-2BGPVS-2BGPVS-2BG
    Modified ScheltensModified ScheltensModified ScheltensModified Scheltens
    PVS-2BG z score/β coefficient (significance)−3.074/−1.094 (<.001)−3.161/−1.002 (<.01)−2.623/−1.956 (<.01)2.212/0.757 (<.05)
    Modified Scheltens z score/β coefficient (significance)−1.928/−1.221 (NS)−1.82/−0.951 (NS)−2.537/−2.727 (<.05)1.674/0.498 (NS)
    Area under ROC curve0.8550.7740.9280.7135
    Sensitivity (%)94.178.991.865.3
    Specificity (%)71.173.684.671.4
    Positive predictive value (%)83.175.083.880.0
    Negative predictive value (%)88.977.891.754.1
    • Note:—NS indicates not significant.

    • ↵a Diagnoses were treated as categories (AD = 1, VaD = 2, and Healthy = 3). Patient age and sex were entered as covariates in each model. All imaging variables were standardized by calculation of z scores (β/standard error) and were entered into the model if they showed a baseline correlation with the diagnosis with significance < .05. Individual z score, β coefficients, and significance are given for each imaging variable in the final model.

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American Journal of Neuroradiology: 36 (5)
American Journal of Neuroradiology
Vol. 36, Issue 5
1 May 2015
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Cite this article
T.P. Hansen, J. Cain, O. Thomas, A. Jackson
Dilated Perivascular Spaces in the Basal Ganglia Are a Biomarker of Small-Vessel Disease in a Very Elderly Population with Dementia
American Journal of Neuroradiology May 2015, 36 (5) 893-898; DOI: 10.3174/ajnr.A4237

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Dilated Perivascular Spaces in the Basal Ganglia Are a Biomarker of Small-Vessel Disease in a Very Elderly Population with Dementia
T.P. Hansen, J. Cain, O. Thomas, A. Jackson
American Journal of Neuroradiology May 2015, 36 (5) 893-898; DOI: 10.3174/ajnr.A4237
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