Medical Research Institute, University of Dundee, Dundee, UK.
Medical Research Institute, University of Dundee, Dundee, UK.
Lancet Diabetes Endocrinol. 2014 Jun;2(6):481-7. doi: 10.1016/S2213-8587(14)70050-6. Epub 2014 Mar 19.
Metformin is a first-line oral agent used in the treatment of type 2 diabetes, but glycaemic response to this drug is highly variable. Understanding the genetic contribution to metformin response might increase the possibility of personalising metformin treatment. We aimed to establish the heritability of glycaemic response to metformin using the genome-wide complex trait analysis (GCTA) method.
In this GCTA study, we obtained data about HbA1c concentrations before and during metformin treatment from patients in the Genetics of Diabetes Audit and Research in Tayside Scotland (GoDARTS) study, which includes a cohort of patients with type 2 diabetes and is linked to comprehensive clinical databases and genome-wide association study data. We applied the GCTA method to estimate heritability for four definitions of glycaemic response to metformin: absolute reduction in HbA1c; proportional reduction in HbA1c; adjusted reduction in HbA1c; and whether or not the target on-treatment HbA1c of less than 7% (53 mmol/mol) was achieved, with adjustment for baseline HbA1c and known clinical covariates. Chromosome-wise heritability estimation was used to obtain further information about the genetic architecture.
5386 individuals were included in the final dataset, of whom 2085 had enough clinical data to define glycaemic response to metformin. The heritability of glycaemic response to metformin varied by response phenotype, with a heritability of 34% (95% CI 1-68; p=0·022) for the absolute reduction in HbA1c, adjusted for pretreatment HbA1c. Chromosome-wise heritability estimates suggest that the genetic contribution is probably from individual variants scattered across the genome, which each have a small to moderate effect, rather than from a few loci that each have a large effect.
Glycaemic response to metformin is heritable, thus glycaemic response to metformin is, in part, intrinsic to individual biological variation. Further genetic analysis might enable us to make better predictions for stratified medicine and to unravel new mechanisms of metformin action.
Wellcome Trust.
二甲双胍是治疗 2 型糖尿病的一线口服药物,但该药的血糖反应差异很大。了解药物反应的遗传贡献可能会增加二甲双胍个体化治疗的可能性。本研究旨在使用全基因组复杂性状分析(GCTA)方法确定二甲双胍血糖反应的遗传度。
在这项 GCTA 研究中,我们从苏格兰泰赛德糖尿病审计和研究遗传学(GoDARTS)研究中的患者中获得了服用二甲双胍前后的糖化血红蛋白(HbA1c)浓度数据,该研究包括了 2 型糖尿病患者队列,并与综合临床数据库和全基因组关联研究数据相关联。我们应用 GCTA 方法估计了 4 种二甲双胍血糖反应定义的遗传度:HbA1c 的绝对降低;HbA1c 的相对降低;调整后的 HbA1c 降低;以及是否达到治疗目标的 HbA1c<7%(53mmol/mol),同时调整了基线 HbA1c 和已知的临床协变量。基于染色体的遗传度估计可提供有关遗传结构的更多信息。
最终数据集纳入了 5386 名个体,其中 2085 名个体有足够的临床数据来定义二甲双胍的血糖反应。二甲双胍血糖反应的遗传度因反应表型而异,调整预处理 HbA1c 后,HbA1c 绝对降低的遗传度为 34%(95%CI 1-68;p=0.022)。基于染色体的遗传度估计表明,遗传贡献可能来自基因组中分散的个体变异,每个变异的影响较小到中等,而不是来自具有较大影响的少数几个位点。
二甲双胍的血糖反应是可遗传的,因此二甲双胍的血糖反应在一定程度上是个体生物学变异的内在因素。进一步的遗传分析可能使我们能够更好地进行分层医学预测,并揭示二甲双胍作用的新机制。
惠康信托基金会。