Genetic Variants in CPA6 and PRPF31 Are Associated With Variation in Response to Metformin in Individuals With Type 2 Diabetes

Metformin is the first-line treatment for type 2 diabetes (T2D). Although widely prescribed, the glucose-lowering mechanism for metformin is incompletely understood. Here, we used a genome-wide association approach in a diverse group of individuals with T2D from the Action to Control Cardiovascular Risk in Diabetes (ACCORD) clinical trial to identify common and rare variants associated with HbA response to metformin treatment and followed up these findings in four replication cohorts. Common variants in and were associated with worse and better metformin response, respectively ( < 5 × 10 ), and meta-analysis in independent cohorts displayed similar associations with metformin response ( = 1.2 × 10 and = 0.005, respectively). Previous studies have shown that (+/-) knockout mice have increased total body fat ( = 1.78 × 10 ) and increased fasted circulating glucose ( = 5.73 × 10 ). Furthermore, rare variants in associated with worse metformin response (