White matter hyperintensity longitudinal morphometric analysis in association with Alzheimer disease

Author:

Strain Jeremy Fuller1,Phuah Chia‐Ling12,Adeyemo Babatunde1,Cheng Kathleen13,Womack Kyle B.1,McCarthy John4,Goyal Manu5,Chen Yasheng1,Sotiras Aristeidis56,An Hongyu5,Xiong Chengjie7,Scharf Andrea8,Newsom‐Stewart Catherine9,Morris John Carl110,Benzinger Tammie Lee Smith510,Lee Jin‐Moo135,Ances Beau M.13510,

Affiliation:

1. Department of Neurology Washington University School of Medicine St. Louis Missouri USA

2. NeuroGenomics and Informatics Center Washington University School of Medicine St. Louis Missouri USA

3. Department of Biomedical Engineering Washington University in St. Louis St. Louis Missouri USA

4. Department of Mathematics Washington University School of Medicine St. Louis Missouri USA

5. Department of Radiology Washington University School of Medicine St. Louis Missouri USA

6. Institute for Informatics Washington University School of Medicine St. Louis Missouri USA

7. Division of Biostatics Washington University School of Medicine St. Louis Missouri USA

8. Department of Biological Sciences Missouri University for Science and Technology Rolla Missouri USA

9. Department of Developmental Biology Washington University School of Medicine St. Louis Missouri USA

10. Knight Alzheimer Disease Research Center St. Louis Missouri USA

Abstract

AbstractINTRODUCTIONVascular damage in Alzheimer's disease (AD) has shown conflicting findings particularly when analyzing longitudinal data. We introduce white matter hyperintensity (WMH) longitudinal morphometric analysis (WLMA) that quantifies WMH expansion as the distance from lesion voxels to a region of interest boundary.METHODSWMH segmentation maps were derived from 270 longitudinal fluid‐attenuated inversion recovery (FLAIR) ADNI images. WLMA was performed on five data‐driven WMH patterns with distinct spatial distributions. Amyloid accumulation was evaluated with WMH expansion across the five WMH patterns.RESULTSThe preclinical group had significantly greater expansion in the posterior ventricular WM compared to controls. Amyloid significantly associated with frontal WMH expansion primarily within AD individuals. WLMA outperformed WMH volume changes for classifying AD from controls primarily in periventricular and posterior WMH.DISCUSSIONThese data support the concept that localized WMH expansion continues to proliferate with amyloid accumulation throughout the entirety of the disease in distinct spatial locations.

Funder

National Institutes of Health

National Institute on Aging

National Institute of Biomedical Imaging and Bioengineering

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

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