| Literature DB >> 28986727 |
Chayakrit Krittanawong1,2, Andrew Xanthopoulos3, Takeshi Kitai4, Natalia Branis5, HongJu Zhang6, Marrick Kukin7.
Abstract
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.Entities:
Keywords: DPP-4 gene; DPP-4 inhibitors; Heart failure; Pharmacogenetics; Pharmacogenomics
Mesh:
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Year: 2018 PMID: 28986727 DOI: 10.1007/s10741-017-9655-y
Source DB: PubMed Journal: Heart Fail Rev ISSN: 1382-4147 Impact factor: 4.214