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African Ancestry Analysis and Admixture Genetic Mapping for Proliferative Diabetic Retinopathy in African Americans.

TitleAfrican Ancestry Analysis and Admixture Genetic Mapping for Proliferative Diabetic Retinopathy in African Americans.
Publication TypeJournal Article
Year of Publication2015
AuthorsTandon A, Chen CJ, Penman A, Hancock H, James M, Husain D, Andreoli C, Li X, Kuo JZ, Idowu O, Riche D, Papavasilieou E, Brauner S, Smith SO, Hoadley S, Richardson C, Kieser T, Vazquez V, Chi C, Fernandez M, Harden M, Cotch M F, Siscovick D, Taylor HA, Wilson JG, Reich D, Wong TY, Klein R, Klein BEK, Rotter JI, Patterson N
Secondary AuthorsSobrin L
JournalInvest Ophthalmol Vis Sci
Volume56
Issue6
Pagination3999-4005
Date Published2015 Jun
ISSN1552-5783
KeywordsAdult, African Americans, Aged, Blood Pressure, Case-Control Studies, Chromosome Mapping, Diabetes Mellitus, Type 2, Diabetic Retinopathy, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Genotype, Glycated Hemoglobin A, Humans, Male, Middle Aged, Odds Ratio, Regression Analysis, Risk Factors
Abstract

PURPOSE: To examine the relationship between proportion of African ancestry (PAA) and proliferative diabetic retinopathy (PDR) and to identify genetic loci associated with PDR using admixture mapping in African Americans with type 2 diabetes (T2D).

METHODS: Between 1993 and 2013, 1440 participants enrolled in four different studies had fundus photographs graded using the Early Treatment Diabetic Retinopathy Study scale. Cases (n = 305) had PDR while controls (n = 1135) had nonproliferative diabetic retinopathy (DR) or no DR. Covariates included diabetes duration, hemoglobin A1C, systolic blood pressure, income, and education. Genotyping was performed on the Affymetrix platform. The association between PAA and PDR was evaluated using logistic regression. Genome-wide admixture scanning was performed using ANCESTRYMAP software.

RESULTS: In the univariate analysis, PDR was associated with increased PAA (odds ratio [OR] = 1.36, 95% confidence interval [CI] = 1.16-1.59, P = 0.0002). In multivariate regression adjusting for traditional DR risk factors, income and education, the association between PAA and PDR was attenuated and no longer significant (OR = 1.21, 95% CI = 0.59-2.47, P = 0.61). For the admixture analyses, the maximum genome-wide score was 1.44 on chromosome 1.

CONCLUSIONS: In this largest study of PDR in African Americans with T2D to date, an association between PAA and PDR is not present after adjustment for clinical, demographic, and socioeconomic factors. No genome-wide significant locus (defined as having a locus-genome statistic > 5) was identified with admixture analysis. Further analyses with even larger sample sizes are needed to definitively assess if any admixture signal for DR is present.

DOI10.1167/iovs.15-16674
Alternate JournalInvest Ophthalmol Vis Sci
PubMed ID26098467
PubMed Central IDPMC4477259
Grant ListZ01 EY000426-05 / / Intramural NIH HHS / United States
Z99 EY999999 / / Intramural NIH HHS / United States
ZIA EY000403-13 / / Intramural NIH HHS / United States
ZIA EY000426-10 / / Intramural NIH HHS / United States
ZIA EY000425-06 / / Intramural NIH HHS / United States
ZIA EY000426-13 / / Intramural NIH HHS / United States
ZIA EY000403-14 / / Intramural NIH HHS / United States
K12 EY016335 / EY / NEI NIH HHS / United States
ZIA EY000426-08 / / Intramural NIH HHS / United States
ZIA EY000403-11 / / Intramural NIH HHS / United States
K12-EY16335 / EY / NEI NIH HHS / United States
UL1 TR000124 / TR / NCATS NIH HHS / United States
Z01 EY000426-04 / / Intramural NIH HHS / United States
ZIA EY000426-11 / / Intramural NIH HHS / United States
ZIA EY000403-10 / / Intramural NIH HHS / United States
P30 DK063491 / DK / NIDDK NIH HHS / United States
ZIA EY000403-09 / / Intramural NIH HHS / United States
Z01 EY000403-06 / / Intramural NIH HHS / United States
ZIA EY000403-08 / / Intramural NIH HHS / United States
N01HC65226 / HL / NHLBI NIH HHS / United States
Z01 EY000403-07 / / Intramural NIH HHS / United States
ZIA EY000426-09 / / Intramural NIH HHS / United States
ZIA EY000426-07 / / Intramural NIH HHS / United States
ZIA EY000426-12 / / Intramural NIH HHS / United States
ZIA EY000426-06 / / Intramural NIH HHS / United States
ZIA EY000403-15 / / Intramural NIH HHS / United States
Z01 EY000425-04 / / Intramural NIH HHS / United States
ZIA EY000403-12 / / Intramural NIH HHS / United States