Volume 10 Supplement 2

Proceedings of the 2012 Sino-American Symposium on Clinical and Translational Medicine (SAS-CTM)

Open Access

Pharmacogenomics in type 2 diabetes management: towards personalized medicine

Journal of Translational Medicine201210(Suppl 2):A19


Published: 17 October 2012

There is inter-individual variability in the responses to anti-diabetic treatments, partly due to genetic factors involved in drug absorption, distribution, metabolism and target. The identification of genetic markers related to drug reaction can help physicians with the decisions of drug selection, dose titration, treatment duration, and avoidance of advert drug reactions. We focused on the effects of susceptibility genes for T2D on anti-diabetic drugs’ efficacy. With respect to repaglinide, genetic variants at multiple loci such as CYP2C8, SLCO1B1, KCNJ11, TCF7L2 and SLC30A8, affect either its pharmacokinetics or pharmacodynamics. We also made some efforts on pharmacogenetic studies of repaglinide efficacy. We recruited a total of 104 Chinese patients with type 2 diabetes and with no history of prior antidiabetic medications, to whom subsequent repaglinide monotherapy with a 48-week follow-up was applied. Based on studies on this cohort, genetic variations at KCNJ11, ABCC8, NOS1AP and KCNQ1 were found to be associated with repaglinide efficacy. Moreover, we also focused on investigations into possible genetic factors for rosiglitazone efficacy, and have already suggested effects of ABCA1 and SLC30A8 variants on the response to rosiglitazone treatment. In spite of all these advances in the field of pharmacogenetics of type 2 diabetes, the pace of clinical application of these findings is rather slow. Consequently, more researches especially randomized clinical trials into the practical utility should be conducted.

Authors’ Affiliations

Shanghai Diabetes Institute, Department of Endocrinology and Metabolism, Shanghai Clinical Center for Diabetes, Shanghai Key Laboratory for Diabetes, Shanghai Jiao Tong University Affiliated Sixth People’s Hospital


© Hu; licensee BioMed Central Ltd. 2012

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.