He Fazhong, Liu Mouze, Chen Zhangren, Liu Guojing, Wang Zhenmin, Liu Rong, Luo Jianquan, Tang Jie, Wang Xingyu, Liu Xin, Zhou Honghao, Chen Xiaoping, Liu Zhaoqian, Zhang Wei
Department of Clinical Pharmacology, Xiangya Hospital, Central South University, Changsha 410008, China; Hunan Key Laboratory of Pharmacogenetics, Institute of Clinical Pharmacology, Central South University, Changsha 410078, China.
Hunan Key Laboratory of Pharmacogenetics, Institute of Clinical Pharmacology, Central South University, Changsha 410078, China.
EBioMedicine. 2016 Nov;13:181-189. doi: 10.1016/j.ebiom.2016.10.025. Epub 2016 Oct 20.
Effects of human tribbles homolog 3 (TRIB3) genetic variation (c.251 A>G, Gln84Arg, rs2295490) on the clinical outcomes of vascular events has not been evaluated in patients with type 2 diabetes after blood pressure lowering and glucose controlling treatment. We did an analysis of a 2×2 factorial (glucose control axis and blood pressure lowering axis) randomized controlled clinical trial at 61 centers in China, with a follow-up period of 5years. The major vascular endpoints were the composites of death from cardio-cerebral vascular diseases, non-fatal stroke and myocardial infraction, new or worsening renal and diabetic eye disease. A total of 1884 participants were included in our research with a 4.8years median follow-up. For glucose lowering axis, patients with TRIB3 (rs2295490) AA (n=609) genotype exhibited significantly reduced risk of major vascular events compared with AG+GG (n=335) genotype carriers (Hazard ratio 0.72, 95% CI 0.55-0.94, p=0.016), Paradoxically, the risk of vascular events were significantly increased in patients with AA (n=621) compared to AG+GG (n=319) genotype for intensive glucose control (Hazard ratio 1.46, 95% CI, 1.06–2.17, p = 0.018) [corrected]. . For blood pressure lowering axis, marginally significant difference was found between TRIB3 variant and coronary events. Our findings suggest that good glucose and blood pressure control exhibited greater benefits on vascular outcomes in patients with TRIB3 (rs2295490) G allele.
在进行血压降低和血糖控制治疗后,人类TRIB3同源物3(TRIB3)基因变异(c.251 A>G,Gln84Arg,rs2295490)对2型糖尿病患者血管事件临床结局的影响尚未得到评估。我们在中国61个中心进行了一项2×2析因(血糖控制轴和血压降低轴)随机对照临床试验,随访期为5年。主要血管终点为心脑血管疾病死亡、非致死性中风和心肌梗死、新发或恶化的肾脏及糖尿病眼病的复合终点。共有1884名参与者纳入我们的研究,中位随访时间为4.8年。对于血糖降低轴,与AG+GG(n=335)基因型携带者相比,TRIB3(rs2295490)AA(n=609)基因型患者发生主要血管事件的风险显著降低(风险比0.72,95%可信区间0.55-0.94,p=0.016)。矛盾的是,强化血糖控制时,AA(n=621)基因型患者与AG+GG(n=319)基因型患者相比,血管事件风险显著增加(风险比1.46,95%可信区间1.06–2.17,p = 0.018)[校正后]。对于血压降低轴,TRIB3变异与冠状动脉事件之间存在边缘显著差异。我们的研究结果表明,良好的血糖和血压控制对携带TRIB3(rs2295490)G等位基因的患者的血管结局具有更大益处。