Osteoarthritis Was Associated With a Faster Decline in Hippocampal Volumes in Cognitively Normal Older People
To examine whether osteoarthritis (OA) is associated with a change in adjusted hippocampal volumes (HpVR: hippocampal/intracranial volume × 10 ) over time among cognitively normal older people. We examined the cross-sectional and longitudinal associations of OA with HpVR among individuals with norma...
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Published in | Frontiers in aging neuroscience Vol. 12; p. 190 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Research Foundation
14.08.2020
Frontiers Media S.A |
Subjects | |
Online Access | Get full text |
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Summary: | To examine whether osteoarthritis (OA) is associated with a change in adjusted hippocampal volumes (HpVR: hippocampal/intracranial volume × 10
) over time among cognitively normal older people.
We examined the cross-sectional and longitudinal associations of OA with HpVR among individuals with normal cognition (NC) from the Alzheimer's Disease Neuroimaging Initiative (ADNI) study. At baseline, a total of 372 individuals with NC were included.
In the cross-sectional analyses of baseline data, we did not find a significant relationship between OA and HpVR among individuals with NC. However, in the longitudinal analyses, OA was significantly associated with change in HpVR over time among individuals with NC. Specifically, compared with individuals without OA, those with OA showed a faster decline in HpVR over time when controlling for other potential confounders, including age, educational attainment, gender, and APOE4 genotype.
OA status was significantly associated with a change in HpVR over time among individuals with NC. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Reviewed by: Kewei Chen, Banner Alzheimer’s Institute, United States; Wen-Cheng Xiong, Case Western Reserve University, United States; Ana Capuano, Rush University, United States Data used in preparation of this article were obtained from the Alzheimer’s Disease Neuroimaging Initiative (ADNI) database (adni.loni.usc.edu). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. A complete listing of ADNI investigators can be found at: http://adni.loni.usc.edu/wp-content/uploads/how_to_apply/ADNI_Acknowledgement_List.pdf Edited by: Gjumrakch Aliev, GALLY International Biomedical Research & Consulting LLC, United States |
ISSN: | 1663-4365 1663-4365 |
DOI: | 10.3389/fnagi.2020.00190 |