The effect of Alzheimer's disease genetic factors on limbic white matter microstructure

AD risk variants in TMEM106B, PTK2B, WNT3, and APOE genes showed distinct associations with limbic FW-corrected WM microstructure metrics. Interaction effects were observed between MS4A6A variants and cognitive status. PGS for AD was associated with higher FW content in the limbic system.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2025-04-01
DOI
https://doi.org/10.1002/alz.70130
Citations
5
Primary Topic
Advanced Neuroimaging Techniques and Applications
Type
article
Field-Weighted Citation Impact
6.80

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article

The effect of Alzheimer's disease genetic factors on limbic white matter microstructure

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5 citations
Alzheimer s & Dementia
Advanced Neuroimaging Techniques and Applications
6.80
article

The effect of Alzheimer's disease genetic factors on limbic white matter microstructure

Susan M. Resnick, Nancy R. Newlin, Timothy J. Hohman, Karthik Ramadass, Arthur W. Toga, T. Bryan Jackson, Niranjana Shashikumar, Sarah Biber, Shannon L. Risacher, Chenyu Gao, Barbara B. Bendlin, Julie A. Schneider, Mohamad Habes, Andrew J. Saykin, Lisa L. Barnes, Derek B. Archer, Logan C. Dumitrescu, Di Wang, Christos A. Davatzikos, Lori L. Beason‐Held, Praitayini Kanakaraj, Guray Erus, Konstantinos Arfanakis, Kurt G. Schilling, Walter A. Kukull, Michael E. Kim, Tianyuan Yao, Angela Lee Jefferson, Yuankai Huo, Kimberly R. Pechman, Bennett A. Landman, Duygu Tosun, Elizabeth C. Mormino, Alaina Durant, Dimitrios Zaras, Zhiyuan Li, Panpan Zhang, Yang An, Paul M. Thompson, Marilyn Albert, Nazirah Mohd Khairi, Sterling C. Johnson, David A. Bennett, Aditi Sathe, Yisu Yang, Anna Lorenz, Abigail W. Workmeister
article en
5 citations

Abstract

AD risk variants in TMEM106B, PTK2B, WNT3, and APOE genes showed distinct associations with limbic FW-corrected WM microstructure metrics. Interaction effects were observed between MS4A6A variants and cognitive status. PGS for AD was associated with higher FW content in the limbic system.

Alzheimer s & DementiaVol. 21(4)
University of Southern California (US), Rush University Medical Center (US), National Institutes of Health (US), University of Wisconsin–Madison (US), Johns Hopkins University (US), The University of Texas at San Antonio Health Science Center (US), University of California, San Francisco (US), Illinois Institute of Technology (US), Vanderbilt University (US), University of Washington (US), University of California System (US), Institute for Neurodegenerative Disorders (US), National Institute on Aging (US), Indiana University School of Medicine, Indiana University – Purdue University Indianapolis (US), University of Pennsylvania (US), Vanderbilt University Medical Center (US), Stanford University (US)
U.S. Department of Defense, Alzheimer's Association, Bristol-Myers Squibb, Alzheimer's Drug Discovery Foundation, Eli Lilly and Company, Pfizer, Illinois Department of Public Health, Biogen, Vanderbilt University, Meso Scale Diagnostics, BioClinica, Novartis Pharmaceuticals Corporation, Takeda Pharmaceutical Company, Northern California Institute for Research and Education, Vanderbilt University Medical Center, Fujirebio Europe, Servier, H. Lundbeck A/S, IXICO, National Institutes of Health, Genentech, GE Healthcare, Canadian Institutes of Health Research, National Institute on Aging, National Institute of Biomedical Imaging and Bioengineering
Openalex Percentile: Top 3%
Advanced Neuroimaging Techniques and Applications
6.80
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