Multivariate Pattern Analysis of Volumetric Neuroimaging Data and Its Relationship With Cognitive Function in Treated HIV Disease.

TitleMultivariate Pattern Analysis of Volumetric Neuroimaging Data and Its Relationship With Cognitive Function in Treated HIV Disease.
Publication TypeJournal Article
Year of Publication2018
AuthorsUnderwood, J, Cole, JH, Leech, R, Sharp, DJ, Winston, A
Corporate AuthorsCHARTER Group
JournalJ Acquir Immune Defic Syndr
Volume78
Issue4
Pagination429-436
Date Published2018 08 01
ISSN1944-7884
KeywordsAdolescent, Adult, Aged, Aged, 80 and over, AIDS Dementia Complex, Biostatistics, Female, HIV Infections, Humans, Image Processing, Computer-Assisted, Longitudinal Studies, Machine Learning, Male, Middle Aged, Neuroimaging, Prognosis, Young Adult
Abstract

BACKGROUND: Accurate prediction of longitudinal changes in cognitive function would potentially allow for targeted intervention in those at greatest risk of cognitive decline. We sought to build a multivariate model using volumetric neuroimaging data alone to accurately predict cognitive function.METHODS: Volumetric T1-weighted neuroimaging data from virally suppressed HIV-positive individuals from the CHARTER cohort (n = 139) were segmented into gray and white matter and spatially normalized before entering into machine learning models. Prediction of cognitive function at baseline and longitudinally was determined using leave-one-out cross-validation. In addition, a multivariate model of brain aging was used to measure the deviation of apparent brain age from chronological age and assess its relationship with cognitive function.RESULTS: Cognitive impairment, defined using the global deficit score, was present in 37.4%. However, it was generally mild and occurred more commonly in those with confounding comorbidities (P < 0.001). Although multivariate prediction of cognitive impairment as a dichotomous variable at baseline was poor (area under the receiver operator curve 0.59), prediction of the global T-score was better than a comparable linear model (adjusted R = 0.08, P < 0.01 vs. adjusted R = 0.01, P = 0.14). Accurate prediction of longitudinal changes in cognitive function was not possible (P = 0.82). Brain-predicted age exceeded chronological age by mean (95% confidence interval) 1.17 (-0.14 to 2.53) years but was greatest in those with confounding comorbidities [5.87 (1.74 to 9.99) years] and prior AIDS [3.03 (0.00 to 6.06) years].CONCLUSION: Accurate prediction of cognitive impairment using multivariate models using only T1-weighted data was not achievable, which may reflect the small sample size, heterogeneity of the data, or that impairment was usually mild.

DOI10.1097/QAI.0000000000001687
Alternate JournalJ Acquir Immune Defic Syndr
PubMed ID29608444
PubMed Central IDPMC6019188
Grant ListHHSN271201000030C / MH / NIMH NIH HHS / United States
HHSN271201000036C / MH / NIMH NIH HHS / United States
N01 MH022005 / MH / NIMH NIH HHS / United States
NIHR-RP-011-048 / / Department of Health / United Kingdom