Candidate gene association study for diabetic retinopathy in persons with type 2 diabetes: the Candidate gene Association Resource (CARe).

Journal Article (Journal Article)

PURPOSE: To investigate whether variants in cardiovascular candidate genes, some of which have been previously associated with type 2 diabetes (T2D), diabetic retinopathy (DR), and diabetic nephropathy (DN), are associated with DR in the Candidate gene Association Resource (CARe). METHODS: Persons with T2D who were enrolled in the study (n = 2691) had fundus photography and genotyping of single nucleotide polymorphisms (SNPs) in 2000 candidate genes. Two case definitions were investigated: Early Treatment Diabetic Retinopathy Study (ETDRS) grades ≥ 14 and ≥ 30. The χ² analyses for each CARe cohort were combined by Cochran-Mantel-Haenszel (CMH) pooling of odds ratios (ORs) and corrected for multiple hypothesis testing. Logistic regression was performed with adjustment for other DR risk factors. Results from replication in independent cohorts were analyzed with CMH meta-analysis methods. RESULTS: Among 39 genes previously associated with DR, DN, or T2D, three SNPs in P-selectin (SELP) were associated with DR. The strongest association was to rs6128 (OR = 0.43, P = 0.0001, after Bonferroni correction). These associations remained significant after adjustment for DR risk factors. Among other genes examined, several variants were associated with DR with significant P values, including rs6856425 tagging α-l-iduronidase (IDUA) (P = 2.1 × 10(-5), after Bonferroni correction). However, replication in independent cohorts did not reveal study-wide significant effects. The P values after replication were 0.55 and 0.10 for rs6128 and rs6856425, respectively. CONCLUSIONS: Genes associated with DN, T2D, and vascular diseases do not appear to be consistently associated with DR. A few genetic variants associated with DR, particularly those in SELP and near IDUA, should be investigated in additional DR cohorts.

Full Text

Duke Authors

Cited Authors

  • Sobrin, L; Green, T; Sim, X; Jensen, RA; Tai, ES; Tay, WT; Wang, JJ; Mitchell, P; Sandholm, N; Liu, Y; Hietala, K; Iyengar, SK; Family Investigation of Nephropathy and Diabetes-Eye Research Group, ; Brooks, M; Buraczynska, M; Van Zuydam, N; Smith, AV; Gudnason, V; Doney, ASF; Morris, AD; Leese, GP; Palmer, CNA; Wellcome Trust Case Control Consortium 2, ; Swaroop, A; Taylor, HA; Wilson, JG; Penman, A; Chen, CJ; Groop, P-H; Saw, S-M; Aung, T; Klein, BE; Rotter, JI; Siscovick, DS; Cotch, MF; Klein, R; Daly, MJ; Wong, TY

Published Date

  • September 29, 2011

Published In

Volume / Issue

  • 52 / 10

Start / End Page

  • 7593 - 7602

PubMed ID

  • 21873659

Pubmed Central ID

  • PMC3183981

Electronic International Standard Serial Number (EISSN)

  • 1552-5783

Digital Object Identifier (DOI)

  • 10.1167/iovs.11-7510


  • eng

Conference Location

  • United States