Exploring the role of Glucagon-Like Peptide-1 in heart failure with preserved ejection fraction among patients with type 2 Diabetes Mellitus

Document Type : Original Article

Authors

1 Internal Medicine Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt

2 Clinical Pathology Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt

3 Cardiology Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt

Abstract

Background: The prevalence of cardiac dysfunction in people with type 2 diabetes mellitus (DM) is as high as 35 %. Type 2 diabetes is associated with the development of heart failure with preserved ejection fraction (HFpEF) than with heart failure with reduced ejection fraction (HFrEF)A considerable number of studies have pointed to the advantageous effects of Glucagon Like Peptide-1(GLP-1) on cardiovascular function. Methods: This case-control study was conducted on 48 subjects of them 16 subjects were healthy control (Group I) , 16 subjects formed the type 2 DM without HF group (Group II), and 16 subjects formed the type 2 DM with HFpEF group (Group III). All patients underwent trans-thoracic echocardiography, routine laboratory tests and measurement of fasting levels of serum GLP-1 by (ELISA) kits. The study was conducted in Internal Medicine Department in collaboration with Cardiology Department and Clinical pathology Department, Faculty of Medicine, Zagazig University Hospitals Results: GLP-1 (pmol/L) level was lowest among diabetics with HFpEF  followed by patients with diabetes without HF and the highest level was among the healthy controls.  A statistically significant negative correlation between GLP-1 and H2FPEF score has been detected among population with type 2 DM. In univariable logistic regression model to assess predictors of HFpEF among patients with type 2 DM, GLP-1 was the only predictor for HFpEF among diabetic patients Conclusion: Low levels of GLP-1 carry a potential risk for HFpEF development among patients with type 2 diabetes; this points to the causation relation between GLP-1 decline and HFpEF occurrence.

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