Bridging Neuroimaging and Pathology in Dementia: A Multi‐Cohort Investigation of MRI‐Derived Brain Volumes
These findings highlight the potential of MRI-derived volumetrics as non-invasive biomarkers of underlying Alzheimer's pathology. Our findings demonstrate notable atrophy in medial temporal, lateral temporoparietal, and midline parietal regions, supporting recognized AD patterns of neurodegeneration, consistent with pivotal studies by Habes et al.,(2016), Dickerson et al.,(2009). Associations between amyloid, tau burdens and atrophy in temporal, parietal, and limbic regions underscore their diagnostic value in neurodegeneration.
Authors
- Rajeswar Kumar
- Nicolas Honnorat (ORCID: https://orcid.org/0000-0003-2210-9341)
- Karl Li
- M. L. Cuccaro
- DEREK ARCHER
- Tanweer Rashid
- Sokratis Charisis (ORCID: https://orcid.org/0000-0001-6578-393X)
- C. Davatzikos
- Mariam Mojtabai
- Sachintha Ransara Brandigampala
- Susan M. Resnick
- Ngoc‐Huynh Ho
- Angela L. Jefferson
- Walter W. Kukull
- Mohamad Habes
- David M Martinez
- Andrew J. Saykin
- David H Wang
- Sudha Seshadri
- Di Wang
- Arthur W. Toga
- Shannon L Risacher
- Duygu Tosun
Institutions
- University of Southern California (US)
- Rush University Medical Center (US)
- University of Miami (US)
- The University of Texas at San Antonio Health Science Center (US)
- University of California, San Francisco (US)
- Vanderbilt University (US)
- University of Washington (US)
- Institute for Neurodegenerative Disorders (US)
- Dr. John T. Macdonald Foundation (US)
- Institute on Aging (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)
- The University of Texas Health Science Center at Houston (US)
Publication Details
- Journal
- Alzheimer s & Dementia
- Published
- 2025-12-01
- DOI
- https://doi.org/10.1002/alz70856_105854
- Primary Topic
- Dementia and Cognitive Impairment Research
- Type
- article
- Field-Weighted Citation Impact
- 0.00