Multimodal Phenotyping of Alzheimer's Disease with Longitudinal Magnetic Resonance Imaging and Cognitive Function Data.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
26 03 2020
Historique:
received: 26 09 2019
accepted: 06 03 2020
entrez: 29 3 2020
pubmed: 29 3 2020
medline: 15 12 2020
Statut: epublish

Résumé

Alzheimer's disease (AD) varies a great deal cognitively regarding symptoms, test findings, the rate of progression, and neuroradiologically in terms of atrophy on magnetic resonance imaging (MRI). We hypothesized that an unbiased analysis of the progression of AD, regarding clinical and MRI features, will reveal a number of AD phenotypes. Our objective is to develop and use a computational method for multi-modal analysis of changes in cognitive scores and MRI volumes to test for there being multiple AD phenotypes. In this retrospective cohort study with a total of 857 subjects from the AD (n = 213), MCI (n = 322), and control (CN, n = 322) groups, we used structural MRI data and neuropsychological assessments to develop a novel computational phenotyping method that groups brain regions from MRI and subsets of neuropsychological assessments in a non-biased fashion. The phenotyping method was built based on coupled nonnegative matrix factorization (C-NMF). As a result, the computational phenotyping method found four phenotypes with different combination and progression of neuropsychologic and neuroradiologic features. Identifying distinct AD phenotypes here could help explain why only a subset of AD patients typically respond to any single treatment. This, in turn, will help us target treatments more specifically to certain responsive phenotypes.

Identifiants

pubmed: 32218482
doi: 10.1038/s41598-020-62263-w
pii: 10.1038/s41598-020-62263-w
pmc: PMC7099007
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

5527

Subventions

Organisme : NIGMS NIH HHS
ID : R01 GM124111
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR003167
Pays : United States

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Auteurs

Yejin Kim (Y)

School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, Texas, USA. yejin.kim@uth.tmc.edu.

Xiaoqian Jiang (X)

School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, Texas, USA.

Luca Giancardo (L)

School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, Texas, USA.
Department of Diagnostic and Interventional Imaging, the McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.

Danilo Pena (D)

School of Biomedical Informatics, University of Texas Health Science Center at Houston, Houston, Texas, USA.

Avram S Bukhbinder (AS)

Department of Neurology, the McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.

Albert Y Amran (AY)

Department of Neurology, the McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.

Paul E Schulz (PE)

Department of Neurology, the McGovern Medical School, University of Texas Health Science Center at Houston, Houston, Texas, USA.

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