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Variants in STAU2 associate with metformin response in a type 2 diabetes cohort: a pharmacogenomics study using real-world electronic health record data

Zhang, Y.; Hu, Y.; Ho, K.; Hartzel, D. N.; Abedi, V.; Zand, R.; Williams, M. S.; Lee, M. T. M.

2020-03-20 endocrinology
10.1101/2020.03.18.20037218 medRxiv
Show abstract

Type 2 diabetes mellitus (T2DM) is a major health and economic burden because of the seriousness of the disease and its complications. Improvements in short- and long-term glycemic control is the goal of diabetes treatment. To investigate the longitudinal management of T2DM at Geisinger, we interrogated the electronic health record (EHR) information and identified a T2DM cohort including 125,477 patients using the Electronic Medical Records and Genomics Network (eMERGE) T2DM phenotyping algorithm. We investigated the annual anti-diabetic medication usage and the overall glycemic control using hemoglobin A1c (HbA1c). Metformin remains the most frequently medication despite the availability of the new classes of anti-diabetic medications. Median value of HbA1c decreased to 7% in 2002 and since remained stable, indicating a good glycemic management in Geisinger population. Using metformin as a pilot study, we identified three groups of patients with distinct HbA1c trajectories after metformin treatment. The variabilities in metformin response is mainly explained by the baseline HbA1c. The pharmacogenomic analysis of metformin identified a missense variant rs75740279 (Leu/Val) for STAU2 associated with the metformin response. This strategy can be applied to study other anti-diabeticmedications. Such research will facilitate the translational healthcare for better T2DM management.

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