Abstract

BackgroundIncretin-based drugs are important in the treatment of type 2 diabetes. However, among the incretin-based drugs, glucagon-like peptide-1 receptor agonists (GLP-1-RAs) have been reported to cause gastroesophageal reflux disease (GERD)-like symptoms making it difficult to continue treatment. Therefore, with the aim of clarifying the relationship between incretin-based drugs and GERD-like symptoms, we conducted a pharmacoepidemiological study using the Japanese adverse drug event report database (JADER).MethodsDipeptidyl peptidase-4 inhibitors (DPP-4-Is) and GLP-1-RAs were set as the incretin-based target drugs. The reporting odds ratio (ROR) and the information component (IC) was used for the detection of quantitative signals. Furthermore, we also compared the time to onset of GERD-like symptoms by log-rank test.ResultsGERD-like symptoms were reported in 36 GLP-1-RAs cases (ROR: 5.61, 95% confidence interval (95% CI): 3.95–7.96 and IC: 2.17, 95% CI: 1.66–2.67) and GLP-1-RAs were detected in the signal. In contrast, DPP-4-Is were not detected in the signal.There was no sex difference with regard to the expression time of GERD-like symptoms by GLP-1-RAs (log-rank test, p = 0.5381). However, the expression time of GERD-like symptoms from GLP-1-RAs was shorter in patients older than 70 years of age than that in those younger than 70 years of age (log-rank test, p < 0.0001).ConclusionsThe administration of GLP-1-RA had a higher incidence of GERD-like symptoms earlier than the administration of DPP-4-Is. In this study, although we think that further investigation is necessary, and suggest that patients older than 70 years of age who have been administered GLP-1-RAs need earlier attention to address GERD-like symptoms than younger patients.

Highlights

  • Incretin-based drugs are important in the treatment of type 2 diabetes

  • Glucosedependent insulinotropic polypeptide (GIP), which is mainly secreted by K cells distributed in the duodenum, and glucagon-like peptide-1 (GLP-1), secreted by L cells distributed in the ileum and colon, are known as incretin

  • Signal detection There were 36 reported cases of GLP-1-RA-related gastroesophageal reflux disease (GERD)-like symptoms (ROR: 5.61, 95% confidence interval (CI): 3.95–7.96 and information component (IC): 2.17, 95% confidence interval (95% CI): 1.66–2.67) and GLP-1-RAs were detected in the signal

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Summary

Introduction

Among the incretinbased drugs, glucagon-like peptide-1 receptor agonists (GLP-1-RAs) have been reported to cause gastroesophageal reflux disease (GERD)-like symptoms making it difficult to continue treatment. Glucosedependent insulinotropic polypeptide (GIP), which is mainly secreted by K cells distributed in the duodenum, and glucagon-like peptide-1 (GLP-1), secreted by L cells distributed in the ileum and colon, are known as incretin. These incretins promote insulin secretion from pancreatic β cells in a blood sugar-dependent manner. GLP-1RAs are more effective than conventional sulfonylurea drugs and glinide drugs (conventional insulin secretagogues) for treating type 2 diabetes, in which hypoglycemia and increased body weight are less likely to occur and in which insulin secretion is reduced

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