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Updated: Feb 21, 2026

Author Spotlight: Exploring the Relationship Between Lipotoxicity and HFpEF
Published on: March 29, 2024
DPP-4 inhibitors and heart failure: a potential role for pharmacogenomics
Chayakrit Krittanawong1,2, Andrew Xanthopoulos3, Takeshi Kitai4
1Department 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. Chayakrit.Krittanawong@mountsinai.org.
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.
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