Intracranial atherosclerosis is associated with lower volume in the posterior body and tail of the hippocampus.
Motivation: Intracranial atherosclerosis is a common and deleterious age-related neuropathology, however, its association with brain morphometry has not been investigated. Goal(s): To investigate brain morphometric anomalies associated with intracranial atherosclerosis in a large number of community-based older adults. Approach: Ex-vivo brain MRI and detailed neuropathologic examination were combined on 891 community-based older adults. Deformation-based morphometry (DBM) was used to investigate the association of intracranial atherosclerosis with brain morphometric characteristics voxel-wise. Results: Intracranial atherosclerosis was associated with lower volume in the posterior body and tail of the hippocampus in linear regression models controlling for all other neuropathologies. Impact: Intracranial atherosclerosis is the third age-related neuropathology after Alzheimer’s and limbic-predominant age-related TDP-43 encephalopathy (LATE) that is shown to be independently associated with lower volume of the hippocampus.
Authors
- Sonal Agrawal (ORCID: https://orcid.org/0000-0003-2375-8888)
- Julie A. Schneider (ORCID: https://orcid.org/0000-0003-0756-5007)
- Alifiya Kapasi (ORCID: https://orcid.org/0000-0003-1911-8482)
- Mahir Tazwar (ORCID: https://orcid.org/0000-0002-6270-8798)
- Gobinda Chowdhury (ORCID: https://orcid.org/0000-0002-2122-9547)
- Konstantinos Arfanakis (ORCID: https://orcid.org/0000-0001-9705-597X)
- Arnold M Evia (ORCID: https://orcid.org/0000-0003-2262-890X)
- David A. Bennett
Publication Details
- Journal
- Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
- Published
- 2024-11-26
- DOI
- https://doi.org/10.58530/2024/4066
- Primary Topic
- Cardiovascular Disease and Adiposity
- Type
- article
- Field-Weighted Citation Impact
- 0.00