Department of Internal Medicine, Icahn School of Medicine at Mount Sinai, Mount Sinai St. Luke's and West hospitals, 1 Gustave L. Levy Pl, New York, NY, 10029, USA.
Division of Cardiovascular Disease, Icahn School of Medicine at Mount Sinai, Mount Sinai St. Luke's hospital, Mount Sinai Heart, New York, NY, USA.
Heart Fail Rev. 2018 May;23(3):355-361. doi: 10.1007/s10741-017-9655-y.
There remains an ongoing controversy regarding the safety of dipeptidyl peptidase-4 (DPP-4) inhibitors and the risk of developing heart failure (HF). In addition, none of the animal studies suggested a mechanism for the DPP-4 inhibitors and HF risk. To date, advances in pharmacogenomics have enabled the identification of genetic variants in DPP-4 gene. Studies have shown that genetic polymorphisms in the gene encoding DPP-4 may be associated with potential pathways involved in HF risk. This review discusses the contradictory findings of DPP-4 inhibitors and HF and a potential role for pharmacogenomics. Pharmacogenomics of DPP-4 inhibitors is promising, and genetic information from randomized control trials is urgently needed to gain a full understanding of the safety of DPP-4 inhibitors and the risk of HF.
关于二肽基肽酶-4(DPP-4)抑制剂的安全性和心力衰竭(HF)风险,目前仍存在争议。此外,动物研究也没有提出 DPP-4 抑制剂和 HF 风险的机制。迄今为止,药物基因组学的进步使得能够鉴定 DPP-4 基因中的遗传变异。研究表明,DPP-4 基因编码的基因多态性可能与 HF 风险相关的潜在途径有关。本综述讨论了 DPP-4 抑制剂和 HF 的矛盾发现以及药物基因组学的潜在作用。DPP-4 抑制剂的药物基因组学具有广阔的前景,迫切需要从随机对照试验中获得遗传信息,以充分了解 DPP-4 抑制剂的安全性和 HF 的风险。