DPP-4 inhibitors and heart failure: a potential role for pharmacogenomics

被引:0
|
作者
Chayakrit Krittanawong
Andrew Xanthopoulos
Takeshi Kitai
Natalia Branis
HongJu Zhang
Marrick Kukin
机构
[1] Icahn School of Medicine at Mount Sinai,Department of Internal Medicine
[2] Mount Sinai St. Luke’s and West hospitals,Division of Cardiovascular Disease
[3] Icahn School of Medicine at Mount Sinai,Department of Cardiology
[4] Mount Sinai St. Luke’s hospital,Department of Cardiovascular Medicine
[5] Mount Sinai Heart,Division of Endocrinology, Diabetes and Nutrition
[6] University General Hospital of Larissa,Division of Cardiovascular Disease, Department of Medicine
[7] Kobe City Medical Center General Hospital,undefined
[8] Icahn School of Medicine at Mount Sinai,undefined
[9] Mount Sinai St. Luke’s and West hospitals,undefined
[10] Mayo Clinic,undefined
来源
Heart Failure Reviews | 2018年 / 23卷
关键词
DPP-4 inhibitors; DPP-4 gene; Heart failure; Pharmacogenomics; Pharmacogenetics;
D O I
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中图分类号
学科分类号
摘要
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.
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页码:355 / 361
页数:6
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