Title | APOE alleles' association with cognitive function differs across Hispanic/Latino groups and genetic ancestry in the study of Latinos-investigation of neurocognitive aging (HCHS/SOL). |
Publication Type | Publication |
Year | 2021 |
Authors | Granot-Hershkovitz E, Tarraf W, Kurniansyah N, Daviglus M, Isasi CR, Kaplan R, Lamar M, Perreira KM, Wassertheil-Smoller S, Stickel A, Thyagarajan B, Zeng D, Fornage M, DeCarli CS, González HM, Sofer T |
Journal | Alzheimers Dement |
Volume | 17 |
Issue | 3 |
Pagination | 466-474 |
Date Published | 2021 Mar |
ISSN | 1552-5279 |
Keywords | Aged, aging, Alleles, Alzheimer Disease, Apolipoprotein E4, Caribbean Region, Cognition, Cognitive Dysfunction, Female, Genotype, Hispanic or Latino, Humans, Male, Middle Aged, Neuropsychological Tests, Prospective Studies, South America, United States |
Abstract | INTRODUCTION: Apolipoprotein E (APOE) alleles are associated with cognitive decline, mild cognitive impairment (MCI), and Alzheimer's disease in Whites, but have weaker and inconsistent effects reported in Latinos. We hypothesized that this heterogeneity is due to ancestry-specific genetic effects.METHODS: We investigated the associations of the APOE alleles with significant cognitive decline and MCI in 4183 Latinos, stratified by six Latino backgrounds, and explored whether the proportion of continental genetic ancestry (European, African, and Amerindian) modifies these associations.RESULTS: APOE ε4 was associated with an increased risk of significant cognitive decline (odds ratio [OR] = 1.15, P-value = 0.03), with the strongest association in Cubans (OR = 1.46, P-value = 0.007). APOE-ε2 was associated with decreased risk of MCI (OR = 0.37, P-value = 0.04) in Puerto Ricans. Amerindian genetic ancestry was found to protect from the risk conferred by APOE ε4 on significant cognitive decline.DISCUSSION: Results suggest that APOE alleles' effects on cognitive outcomes differ across six Latino backgrounds and are modified by continental genetic ancestry. |
DOI | 10.1002/alz.12205 |
Alternate Journal | Alzheimers Dement |
PubMed ID | 33155766 |
PubMed Central ID | PMC8016734 |
Grant List | HHSN268201300005C / HL / NHLBI NIH HHS / United States P30 AG059299 / AG / NIA NIH HHS / United States HHSN268201300001C / HL / NHLBI NIH HHS / United States P30 AG062429 / AG / NIA NIH HHS / United States P30 AG010129 / AG / NIA NIH HHS / United States R21 AG056952 / AG / NIA NIH HHS / United States R01 NS017950 / NS / NINDS NIH HHS / United States HHSN268201300004C / HL / NHLBI NIH HHS / United States HHSN268201300003I / HL / NHLBI NIH HHS / United States R01 AG048642 / AG / NIA NIH HHS / United States RF1 AG061022 / AG / NIA NIH HHS / United States R56 AG048642 / AG / NIA NIH HHS / United States RF1 AG054548 / AG / NIA NIH HHS / United States U01 AG052409 / AG / NIA NIH HHS / United States HHSN268201300003C / HL / NHLBI NIH HHS / United States P30 AG066546 / AG / NIA NIH HHS / United States |
APOE alleles' association with cognitive function differs across Hispanic/Latino groups and genetic ancestry in the study of Latinos-investigation of neurocognitive aging (HCHS/SOL).
MS#:
0949
ECI:
Yes
Manuscript Status:
Published