Abstract

BackgroundCoronary artery disease (CAD) shares common risk factors with type 2 diabetes (T2DM). Variations in the transcription factor 7-like 2 (TCF7L2) gene, particularly rs7903146, increase T2DM risk. Potential links between genetic variants of the TCF7L2 locus and coronary atherosclerosis are uncertain. We therefore investigated the association between TCF7L2 polymorphisms and angiographically determined CAD in diabetic and non-diabetic patients.Methodology/Principal FindingsWe genotyped TCF7L2 variants rs7903146, rs12255372, and rs11196205 in a cross-sectional study including 1,650 consecutive patients undergoing coronary angiography for the evaluation of established or suspected stable CAD. Significant CAD was diagnosed in the presence of coronary stenoses ≥50%. Variant rs7903146 in the total study cohort was significantly associated with significant CAD (adjusted additive OR = 1.29 [1.09–1.53]; p = 0.003). This association was strong and significant in T2DM patients (n = 393; OR = 1.91 [1.32–2.75]; p = 0.001) but not in non-diabetic subjects (OR = 1.09 [0.90–1.33]; p = 0.370). The interaction risk allele by T2DM was significant (pinteraction = 0.002), indicating a significantly stronger impact of the polymorphism on CAD in T2DM patients than in non-diabetic subjects. TCF7L2 polymorphisms rs12255372 and rs11196205 were also significantly associated with CAD in diabetic patients (adjusted additive OR = 1.90 [1.31–2.74]; p = 0.001 and OR = 1.75 [1.22–2.50]; p = 0.002, respectively). Further, haplotype analysis demonstrated that haplotypes including the rare alleles of all investigated variants were significantly associated with CAD in the whole cohort as well as in diabetic subjects (OR = 1.22 [1.04–1.43]; p = 0.013 and OR = 1.67 [1.19–2.22]; p = 0.003, respectively).Conclusions/SignificanceThese results suggest that TCF7L2 variants rs7903146 rs12255372, and rs11196205 are significantly associated with angiographically diagnosed CAD, specifically in patients with T2DM. TCF7L2 therefore appears as a genetic link between diabetes and atherosclerosis.

Highlights

  • Type 2 diabetes (T2DM) confers a two- to threefold increased risk of coronary artery disease (CAD) [1,2]

  • Single nucleotide polymorphisms (SNPs) of transcription factor 7-like 2 (TCF7L2) have been consistently associated with T2DM in populations of different ethnic descent, making TCF7L2 one of the most important locus known today to predispose for T2DM [7,8,9]

  • The analysed TCF7L2 SNPs were in linkage disequilibrium: Pairwise squared correlation coefficients were r2 = 0.747 between rs7903146 and rs12255372, r2 = 0.491

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Summary

Introduction

Type 2 diabetes (T2DM) confers a two- to threefold increased risk of coronary artery disease (CAD) [1,2]. T2DM and CAD share common risk factors and both diseases show a strong genetic background [3,4,5]. Among noted SNPs, variant rs7903146 was found to be most significantly associated with T2DM risk [6,7,8,9]. TCF7L2 SNPs rs12255372 and rs11196205 have been linked with impaired glucose metabolism [8,9,10] and an increased diabetes risk. Coronary artery disease (CAD) shares common risk factors with type 2 diabetes (T2DM). Variations in the transcription factor 7-like 2 (TCF7L2) gene, rs7903146, increase T2DM risk. We investigated the association between TCF7L2 polymorphisms and angiographically determined CAD in diabetic and non-diabetic patients

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