Abstract

Aim: To investigate the changes of insulin resistance (IR), parameters of arterial stiffness, concentrations of N-terminal pro-brain natriuretic peptide (NT-proBNP), and echocardiographic parameters in patients with cardiac autonomic neuropathy (CAN) and type 2 diabetes mellitus (T2D). Methods: This study recruited 44 patients with T2D (19 patients without CAN and 25 patients with CAN) and 15 healthy volunteers. Arterial stiffness, immunoreactive insulin, homeostasis model assessment IR, NT-proBNP parameters, and echocardiographic examination were assessed. Results: Development of CAN is associated with increase in NT-proBNP levels, IR parameters, and arterial stiffening. Among patients with CAN, arterial stiffness parameters were considered as high. We found out that among patients of this group, the value of brachial augmentation index was normal in 52%, elevated in 40%, and pathological in 8%; pulse wave velocity was normal in 16%, elevated in 52%, and pathological in 32% of cases. Obtained results showed that development of CAN is accompanied by more pronounced left ventricular diastolic dysfunction and by formation of left ventricular hypertrophy (LVH), mostly by concentric type. Among patients of this group concentric LVH was diagnosed among 76 % and eccentric LVH among 16% of persons. Multiple regression analysis, after controlling for age, sex, diabetes duration, blood pressure, HbA1c, and left ventricular mass index, showed an independent association of heart rate response to deep breathing with pulse wave velocity (P < 0.001). Conclusion: Development of CAN is associated with increased IR parameters, increased levels of NT-proBNP, arterial stiffening, left ventricular diastolic dysfunction, and formation of LVH, mostly by concentric type.

Highlights

  • Myocardial metabolic remodeling occurred over established type 2 diabetes mellitus (T2D) among adult and retired persons; coronary vessels affection, myocardium changes, diabetic cardiomyopathy (DCM), and diabetic cardiac autonomic neuropathy (CAN) are associated with the definition “diabetic heart”[1,2].CAN is a significant risk factor for coronary heart disease, including heart attack, stroke, heart failure (HF), and sudden arrhythmic death

  • Development of CAN is associated with increased insulin resistance (IR) parameters, increased levels of NT-proBNP, arterial stiffening, left ventricular diastolic dysfunction, and formation of left ventricular hypertrophy (LVH), mostly by concentric type

  • That levels of immunoreactive insulin and Homeostasis model assessment IR (HOMA-IR) were elevated among T2D patients without CAN (P < 0.001) compared to the control group, and further increase of these parameters was found among patients with diagnosed CAN

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Summary

Introduction

Myocardial metabolic remodeling occurred over established type 2 diabetes mellitus (T2D) among adult and retired persons; coronary vessels affection, myocardium changes, diabetic cardiomyopathy (DCM), and diabetic cardiac autonomic neuropathy (CAN) are associated with the definition “diabetic heart”[1,2].CAN is a significant risk factor for coronary heart disease, including heart attack, stroke, heart failure (HF), and sudden arrhythmic death. Myocardial metabolic remodeling occurred over established type 2 diabetes mellitus (T2D) among adult and retired persons; coronary vessels affection, myocardium changes, diabetic cardiomyopathy (DCM), and diabetic cardiac autonomic neuropathy (CAN) are associated with the definition “diabetic heart”[1,2]. The independent connection of CAN with the severity of coronary vessels affections in persons with T2D has not been determined[7]. Several epidemiological studies established that increased parameters of arterial stiffness may increase cardiovascular morbidity and mortality, independently from the presence of several other cardiovascular risk factors. Increase of arterial stiffness parameters by diabetes can be due to changes in structure or type of elastin and/or collagen in the arterial wall, chronic low-grade inflammation, increased oxidative stress (OS), reduced bioavailability of nitric oxide (NO), and increased activity of sympathetic nervous system[8,9]

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