首页> 外文期刊>Clinical and experimental medicine >Influence of SLC22A1 rs622342 genetic polymorphism on metformin response in South Indian type 2 diabetes mellitus patients
【24h】

Influence of SLC22A1 rs622342 genetic polymorphism on metformin response in South Indian type 2 diabetes mellitus patients

机译:SLC22A1 rs622342基因多态性对南印度2型糖尿病患者二甲双胍反应的影响

获取原文
获取原文并翻译 | 示例
           

摘要

Metformin is an oral antidiabetic drug, commonly used for treating type 2 diabetes mellitus (T2DM) patients. It is transported into the hepatocytes by polyspecific organic cation transporter 1, which is encoded by the gene SLC22A1. It has been hypothesized that genetic variations of SLC22A1 gene will influence inter-individual variation in glucose lowering efficacy of metformin. Previous studies have demonstrated this in other populations with conflicting results, but it remains to be elucidated in Indian population. Henceforth, the objective of the study was to evaluate the impact of SLC22A1 rs622342 gene polymorphism on the clinical efficacy of metformin in South Indian T2DM patients. A total of 122 newly detected, treatment naive T2DM patients of either sex were included in this study. The patients were started on metformin monotherapy and followed up for 12 weeks. Genotype was determined using qRT-PCR. Before and after treatment with metformin, body mass index (BMI), serum lipid profile, glycated hemoglobin (HbA(1c)), fasting and postprandial glucose level, and blood pressure (BP) were measured. The study cohort mean age was 49.57 +/- A 9.88 years. Of the 122 T2DM patients, 93 were classified as responders and 29 as non-responders based on fall in HbA(1c) levels. Interestingly, carriers of one variant allele 'C' (AC) of rs622342 polymorphism were less among the responders than those who did not (44.8 vs. 22.6 %). The response was even lesser (13.8 vs. 4.3 %) in carriers of two copies of "C" allele (CC). On the contrary, patients with two copies of allele 'A' (AA) had 5.6 times greater chance of responding to metformin treatment. A similar trend was observed when the proportion was analyzed under different genetic models (OR 3.85, 95 % CI 1.61-9.19 for dominant; OR 3.56, 95 % CI 0.83-15.26 for recessive; OR 0.35, 95 % CI 0.14-0.86 for over-dominant; and OR 4.10, 95 % CI 1.78-9.43 for additive). Further, metformin showed significant beneficial effects on BMI, HbA(1c), FPG, PPG, lipid parameters and BP. These data suggest that the allele and genotypes of SLC22A1 rs622342 gene polymorphism were associated with the therapeutic efficacy of metformin in South Indian patients with T2DM.
机译:二甲双胍是一种口服降糖药,通常用于治疗2型糖尿病(T2DM)患者。它由基因SLC22A1编码的多特异性有机阳离子转运蛋白1转运到肝细胞中。据推测,SLC22A1基因的遗传变异将影响个体间的二甲双胍降糖功效。先前的研究已经在其他人群中证明了这一点,但结果相矛盾,但在印度人群中仍有待阐明。今后,该研究的目的是评估SLC22A1 rs622342基因多态性对二甲双胍在南印度T2DM患者中的临床疗效的影响。这项研究总共包括了122名新发现的,治疗过的T2DM男女患者。患者开始接受二甲双胍单药治疗,并随访12周。使用qRT-PCR确定基因型。用二甲双胍治疗前后,测量体重指数(BMI),血清脂质谱,糖化血红蛋白(HbA(1c)),禁食和餐后血糖水平以及血压(BP)。研究队列的平均年龄为49.57 +/- A 9.88岁。根据HbA(1c)水平的下降,在122名T2DM患者中,有93名被分类为有反应者,有29名为无反应者。有趣的是,在应答者中,rs622342多态性的一个变异等位基因“ C”(AC)的携带者比没有应答者的携带者要少(44.8比22.6%)。两份“ C”等位基因(CC)携带者的反应甚至更低(13.8比4.3%)。相反,具有两个等位基因“ A”(AA)的患者对二甲双胍治疗的反应几率高5.6倍。在不同遗传模型下分析比例时观察到相似的趋势(显性为OR 3.85,95%CI 1.61-9.19;隐性为OR 3.56,95%CI 0.83-15.26; OR 0.35,95%CI 0.14-0.86 -占主导;或OR 4.10,添加剂的95%CI 1.78-9.43)。此外,二甲双胍对BMI,HbA(1c),FPG,PPG,脂质参数和BP表现出显着的有益作用。这些数据表明,SLC22A1 rs622342基因多态性的等位基因和基因型与二甲双胍对南印度地区2型糖尿病患者的疗效相关。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号