Laboratory of Genetics and Molecular Cardiology, Heart Institute (InCor), University of São Paulo Medical School, São Paulo, Brazil.
PLoS One. 2009 Nov 17;4(11):e7697. doi: 10.1371/journal.pone.0007697.
TCF7L2 polymorphisms have been consistently associated with type 2 diabetes mellitus in different populations and type 2 diabetes mellitus is a major risk factor for cardiovascular disease, especially coronary artery disease. This study aimed to evaluate the association between TCF7L2 polymorphism rs7903146 and coronary artery disease in diabetic and non-diabetic subjects.
two populations were studied in order to assess severity of coronary artery disease and cardiovascular events incidence. Eight-hundred and eighty nine subjects who were referred for cardiac catheterization for coronary artery disease diagnosis were cross-sectionally evaluated for coronary lesions (atherosclerotic burden) and 559 subjects from the MASS-II Trial were prospectively followed-up for 5 years and assessed for major cardiovascular events incidence. As expected, rs7903146 T allele was associated with diabetes. Although diabetic patients had a higher prevalence of coronary lesions, no association between TCF7L2 genotype and coronary lesions was found in this subgroup. However, non-diabetic individuals carrying the T allele were associated with a significantly higher frequency of coronary lesions than non-diabetic non-carriers of the risk allele (adjusted OR = 2.32 95%CI 1.27-4.24, p = 0.006). Moreover, presence of multi-vessel coronary artery disease was also associated with the CT or TT genotypes in non-diabetics. Similarly, from the prospective sample analysis, non-diabetics carrying the CT/TT genotypes had significantly more composite cardiovascular end-points events than CC carriers (p = 0.049), mainly due to an increased incidence of death (p = 0.004).
rs7903146 T allele is associated with diabetes and, in non-diabetic individuals, with a higher prevalence and severity of coronary artery disease and cardiovascular events. name of registry site (see list below), registration number, trial registration URL in brackets.
MEDICINE, ANGIOPLASTY, OR SURGERY STUDY (MASS II): Unique identifier: ISRCTN66068876.
TCF7L2 多态性与不同人群的 2 型糖尿病一直相关,而 2 型糖尿病是心血管疾病的主要危险因素,特别是冠心病。本研究旨在评估 TCF7L2 多态性 rs7903146 与糖尿病和非糖尿病患者的冠心病之间的关联。
为了评估冠状动脉疾病的严重程度和心血管事件的发生率,研究了两个人群。对 889 名因冠状动脉疾病诊断而接受心脏导管检查的患者进行了横断面评估,以评估冠状动脉病变(动脉粥样硬化负担),并对 MASS-II 试验中的 559 名患者进行了前瞻性随访 5 年,以评估主要心血管事件的发生率。正如预期的那样,rs7903146 T 等位基因与糖尿病有关。尽管糖尿病患者的冠状动脉病变发生率较高,但在该亚组中未发现 TCF7L2 基因型与冠状动脉病变之间存在关联。然而,携带 T 等位基因的非糖尿病患者与非携带风险等位基因的非糖尿病患者相比,冠状动脉病变的频率显著更高(调整后的 OR = 2.32,95%CI 1.27-4.24,p = 0.006)。此外,在非糖尿病患者中,多支冠状动脉疾病的存在也与 CT 或 TT 基因型相关。同样,从前瞻性样本分析中,携带 CT/TT 基因型的非糖尿病患者发生复合心血管终点事件的比例明显高于 CC 携带者(p = 0.049),主要是由于死亡率增加(p = 0.004)。
rs7903146 T 等位基因与糖尿病相关,并且在非糖尿病患者中,与冠状动脉疾病的更高发生率和严重程度以及心血管事件相关。注册号(见下方列表)、试验注册号、试验注册网址(括号内)。
医学、血管成形术或手术研究(MASS II):唯一标识符:ISRCTN66068876。