Abstract

Type 2 diabetes mellitus (T2DM) and chronic heart failure (HF) have close association, and several biomarkers have been studied to better understand this association and improve prediction of HF in T2DM. Furthermore, in recent clinical trials, sodium glucose cotransporter 2 inhibitors (SGLT2i), glucose-lowering drugs, improved HF outcomes. The objective of the present study was to evaluate association between circulating biomarkers of fibrosis and incidence of HF with preserved ejection fraction (HFpEF) in patients with T2DM receiving sodium glucose cotransporter 2 inhibitors (SGLT2i). Materials and Methods. At baseline, transthoracic echocardiography and laboratory assessment of N-terminal fragment of the brain natriuretic peptide (Nt-proBNP), soluble suppression of tumorigenesis-2 (sST2), galectin-3 (Gal-3), C-terminal propeptide of procollagen type I (PICP), N-terminal propeptide of procollagen type III (PIIINP), matrix metalloproteinase-9 (MMP-9), and tissue inhibitor of matrix proteinase-1 (TIMP-1) were done. After 3 years of follow-up, information about HF events (hospitalization for HF, established HF in outpatient department by a cardiologist) was obtained. Results. Seventy-two patients were included in the study. The mean age was 57 (49.7; 63.2) years; 44% were female. Most patients had T2DM for more than 4 years. All patients were overweight or had obesity, and 93% patients had arterial hypertension (AH). After 3 years of follow-up, HFpEF was established in 21% patients. Patients were divided into two groups according to the presence of HFpEF, and baseline characteristics were compared. Patients with HF were older and had longer diabetes and AH duration and higher Nt-proBNP, Gal-3, PIIINP, and PICP levels at baseline than patients without HF (all p < 0.05). Gal − 3 > 10 ng/ml (OR = 2.25; 95% CI, 1.88–5.66; p = 0.01) and NT − pro − BNP > 80 pg/ml (OR = 2.64; 95% CI, 1.56–4.44; p = 0.001) were associated with increased risk of HF incidence. Age > 60 years, diabetes duration > 10 years, and presence of abdominal obesity were independent predictors of HFpEF as well. Conclusions. T2DM patients treated with SLGT2i, who developed HFpEF after 3 years of follow-up, had higher PICP, PIIINP, Gal-3, and NT-proBNP serum concentrations at baseline, and Gal-3 level was an independent predictor of HFpEF.

Highlights

  • Type 2 diabetes mellitus (T2DM) is one of the most important chronic conditions nowadays, which is tightly linked to development of chronic heart failure (HF)

  • The aim of this study was to assess the relationship between circulating biomarkers of fibrosis and the incidence of HF with preserved ejection fraction (HFpEF) in T2DM patients receiving sodium glucose cotransporter 2 inhibitors (SGLT2i)

  • These patients had clinical and laboratory risk factors associated with HF incident

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Summary

Introduction

Type 2 diabetes mellitus (T2DM) is one of the most important chronic conditions nowadays, which is tightly linked to development of chronic heart failure (HF). T2DM can contribute to HF via different mechanisms such as low-grade inflammation, oxidative stress, endothelial dysfunction, and fibrosis [2]. These processes lead to diabetic cardiomyopathy, acceleration of atherosclerosis, increased arterial stiffness, and myocardial ischemia. Several biomarkers have been studied in order to better understand HF development in T2DM and improve the prediction of HF incidence and its progression [3, 4]. The predictive value of circulating biomarkers of fibrosis in a HF incidence and T2DM-induced cardiomyopathy was shown in several

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