A Common DIO2 Polymorphism and Alzheimer Disease Dementia in African and European Americans

TitleA Common DIO2 Polymorphism and Alzheimer Disease Dementia in African and European Americans
Publication TypeJournal Article
Year of Publication2018
AuthorsMcAninch, EA, Rajan, KB, Jo, S, Chaker, L, al., et
JournalJournal of Endocrinology & Metabolism
Volume103
Issue5
Start Page1818
Pagination118-1826
Date Published05/2018
ISSN Number0021-972X
KeywordsAlzheimer's disease, Cognitive Ability, Genome
Abstract

Context
A common single nucleotide polymorphism in DIO2, Thr92AlaD2, has been associated with a transcriptome typically found in neurodegenerative diseases in postmortem human brain tissue.

Objective
To determine whether Thr92AlaD2 is associated with incident Alzheimer disease (AD).

Design
Population-based study; human brain tissue microarray.

Setting
Community-based cohorts from Chicago and northeastern Illinois and religious clergymen from across the United States constituted the primary population. A representative sample of the U.S. population was used for secondary analyses.

Participants
3054 African Americans (AAs) and 9304 European Americans (EAs).

Main Outcome Measure
Incident AD.

Results
In the primary population, AAs with Thr92AlaD2 had 1.3 times [95% confidence interval (CI), 1.02 to 1.68; P = 0.048] greater odds of developing AD. AAs from a second population with Thr92AlaD2 showed a trend toward increased odds of dementia (odds ratio, 1.33; 95% CI, 0.99 to 1.78; P = 0.06) and 1.35 times greater odds of developing cognitive impairment not demented (CIND; 95% CI, 1.09 to 1.67; P = 0.006). Meta-analysis showed that AAs with Thr92AlaD2 had 1.3 times increased odds of developing AD/dementia (95% CI, 1.07 to 1.58; P = 0.008). In EAs, no association was found between Thr92AlaD2 and AD, dementia, or CIND. Microarray of AA brain tissue identified transcriptional patterns linked to AD pathogenesis.

Conclusions
Thr92AlaD2 was associated with molecular markers known to underlie AD pathogenesis in AAs, translating to an observed phenotype of increased odds of developing AD/dementia in AAs in these populations. Thr92AlaD2 might represent one factor contributing to racial discrepancies in incident AD.

URLhttps://academic.oup.com/jcem/article/103/5/1818/4893706
Citation Key9628