Department of Neurology, Philipps University Marburg, Marburg, Germany.
Obes Facts. 2011;4(4):290-6. doi: 10.1159/000330881. Epub 2011 Aug 1.
Studies evaluating genetic markers for vascular risk and risk of stroke are limited, and none of them evaluated obesity genes. The objective was to investigate the genetic markers related to obesity genes FTO and MC4R and the gene of type 2 diabetes mellitus TCF7L2 for their contribution to risk of stroke and transient ischemic attacks (TIA).
We recruited 379 consecutive patients with stroke/TIA and 379 healthy population-based controls. The single-nucleotide polymorphisms (SNPs) rs9937053 (FTO), rs2229616 (MC4R V103I), rs17782313 (188kb downstream of MC4R), and rs7903146 (TCF7L2) were evaluated for association with stroke using logistic regression analyses.
The odds ratios for stroke/TIA were 1.14 (95%CI 0.91-1.42) for rs9937053/FTO, 1.11 (95%CI 0.49-2.51) for rs2229616/MC4R, 1.05 (95%CI 0.82-1.3) for rs17782313/MC4R, and 0.99 (95%CI 0.78-1.25) for rs7903146/TCF7L2. Further exploration revealed that male patients with the T allele of rs7903146/TCF7L2 had a worse clinical outcome compared with male patients carrying the C allele.
The observed trends of obesity risk alleles for risk of stroke/TIA as well as the possible sex-specific differences in clinical outcomes found for the TCF7L2 (rs7903146) require replication in future studies. Our study demonstrates that candidate gene studies for common stroke may benefit from focusing on polymorphisms that predispose to vascular risk.
评估血管风险和中风风险的遗传标志物的研究有限,而且没有一项研究评估肥胖基因。本研究旨在探讨与肥胖基因 FTO 和 MC4R 以及 2 型糖尿病 TCF7L2 相关的遗传标志物,以研究其对中风和短暂性脑缺血发作(TIA)风险的影响。
我们招募了 379 例连续中风/TIA 患者和 379 例健康人群作为对照组。使用 logistic 回归分析评估单核苷酸多态性(SNP)rs9937053(FTO)、rs2229616(MC4R V103I)、rs17782313(MC4R 下游 188kb)和 rs7903146(TCF7L2)与中风的相关性。
rs9937053/FTO 的中风/TIA 比值比(OR)为 1.14(95%可信区间(CI)为 0.91-1.42),rs2229616/MC4R 为 1.11(95%CI 为 0.49-2.51),rs17782313/MC4R 为 1.05(95%CI 为 0.82-1.3),rs7903146/TCF7L2 为 0.99(95%CI 为 0.78-1.25)。进一步的探索显示,携带 rs7903146/TCF7L2 等位基因 T 的男性患者的临床结局较携带等位基因 C 的男性患者更差。
本研究观察到肥胖风险等位基因与中风/TIA 风险之间的趋势,以及 TCF7L2(rs7903146)的可能性别特异性临床结局差异,需要在未来的研究中进行验证。本研究表明,针对常见中风的候选基因研究可能受益于关注易患血管风险的多态性。