Evaluating the association between <i>APOE</i> genotypes and cognitive resilience in SuperAgers

Within our large, harmonized cohort, larger proportions of SuperAgers had APOE-ε2 alleles and smaller proportions had APOE-ε4 alleles than AD cases across both NHW and NHB participants. Crucially, higher proportions of NHW SuperAgers had APOE-ε2 alleles than younger controls (ages<80) and lower proportions had APOE-ε4 alleles than all controls including age-matched controls (ages 80+). This work provides the strongest evidence to date that APOE is associated with SuperAging. APOE-ε2 did not differentiate NHB SuperAgers from controls nor APOE-ε4 from other oldest-old adults in present analyses. Future work will extend to whole genome analysis to identify novel genomic drivers of SuperAging.

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Publication Details

Journal
Alzheimer s & Dementia
Published
2024-12-01
DOI
https://doi.org/10.1002/alz.093260
Primary Topic
Adipose Tissue and Metabolism
Type
article
Field-Weighted Citation Impact
0.00
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article

Evaluating the association between APOE genotypes and cognitive resilience in SuperAgers

Timothy J. Hohman, Weixin Wang, Jonathan L. Haines, Michael L. Lee et al.
Alzheimer s & Dementia
Adipose Tissue and Metabolism
article

Evaluating the association between APOE genotypes and cognitive resilience in SuperAgers

Timothy J. Hohman, Weixin Wang, Jonathan L. Haines, Michael L. Lee, Emily H. Trittschuh, Julie A. Schneider, Andrew J. Saykin, Lisa L. Barnes, Logan C. Dumitrescu, C. Dirk Keene, Lindsay A. Farrer, Michael L. Cuccaro, Carlos C Cruchaga, David Bennett, Corinne D. Engelman, Leslie S. Gaynor, Paul K. Crane, Adam C. Naj, Shubhabrata Mukherjee, Walter A. Kukull, Angela Lee Jefferson, William S. Bush, Phoebe Scollard, Eden R. Martin, Brian W. Kunkle, Badri Narayan Vardarajan, Jesse Mez, Alaina Durant, Paul M. Thompson, Seo‐Eun Choi, Jason J. Hassenstab, Katherine A. Gifford, Sterling C. Johnson, Richard Mayeux, Marilyn S. Albert, Margaret A Pericak‐Vance
article en

Abstract

Within our large, harmonized cohort, larger proportions of SuperAgers had APOE-ε2 alleles and smaller proportions had APOE-ε4 alleles than AD cases across both NHW and NHB participants. Crucially, higher proportions of NHW SuperAgers had APOE-ε2 alleles than younger controls (ages<80) and lower proportions had APOE-ε4 alleles than all controls including age-matched controls (ages 80+). This work provides the strongest evidence to date that APOE is associated with SuperAging. APOE-ε2 did not differentiate NHB SuperAgers from controls nor APOE-ε4 from other oldest-old adults in present analyses. Future work will extend to whole genome analysis to identify novel genomic drivers of SuperAging.

Alzheimer s & DementiaVol. 20(S1)
Boston University (US), University of Southern California (US), Rush University Medical Center (US), NewYork–Presbyterian Hospital (US), University of Wisconsin–Madison (US), Johns Hopkins University (US), University of Miami (US), University of Washington (US), Washington University in St. Louis (US), Columbia University Irving Medical Center (US), Johns Hopkins Medicine (US), New York Hospital Queens (US), VA Puget Sound Health Care System (US), Dr. John T. Macdonald Foundation (US), Indiana University School of Medicine, Indiana University – Purdue University Indianapolis (US), Case Western Reserve University (US), University of Pennsylvania (US), Vanderbilt University Medical Center (US)
Openalex Percentile: Top 65%
Adipose Tissue and Metabolism
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