Dynamics of li pid profile and heart rate variability parameters by omega ‑3 polyunsaturated fatty acids and simvastatin prescription in patients w ith type 2 diabetes mellitus and cardiovascular autonomi c neuropathy
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Keywords

type 2 diabetes mellitus, cardiovascular autonomic neuropathy, lipids, heart rate variability, ω‑3 polyunsaturated fatty acids, statins, combined therapy

How to Cite

Azhmi, S., Serhiyenko, V., & Serhiyenko, A. (2018). Dynamics of li pid profile and heart rate variability parameters by omega ‑3 polyunsaturated fatty acids and simvastatin prescription in patients w ith type 2 diabetes mellitus and cardiovascular autonomi c neuropathy. Endokrynologia, 22(3), 237-244. Retrieved from https://endokrynologia.com.ua/index.php/journal/article/view/83

Abstract

The purpose of this study was to evaluate the peculiarities of ω‑3 polyunsaturated fatty acids (ω‑3 PUFAs) and simvastatin prescription on the blood lipid profile and heart rate variability (HRV) parameters in patients with type 2 diabetes mellitus (T2DM) and functional stage of cardiovascular autonomic neuropathy (CAN). Materials and methods. The study involved 75 patients with T2DM and functional stage of CAN aged 50-59 years, HbA1c (7.1±0.4)%, who received traditional hypoglycemic therapy within 3 months. Patients were stratified into four groups: 21 patients received 1 capsule/day of ω‑3 PUFAs in addition to hypoglycemic therapy; 22 patients received simvastatin 20 mg/day; 17 patients
received 1 g/day of ω‑3-PUFAs and simvastatin 10 mg/day; control group (n=15). The duration of the study was 3 month. Results. The prescription of ω‑3 PUFAs promoted to the more significant decrease in triglycerides (TG) level compared to treatment with simvastatin, a significant decrease of atherogenic coefficient (AC), and an increase of high-density lipoprotein-cholesterol (HDL-C) and, at the same time, did not affect the concentration of the total cholesterol and low density lipoprotein-cholesterol (LDL-cholesterol). Treatment with simvastatin was accompanied by the significant decrease in total cholesterol, LDL cholesterol, TG, AC and an increase in HDL cholesterol; significant decrease in total cholesterol, LDL-cholesterol and TG levels (compared to the ω‑3 PUFAs). Prescription of ω‑3 PUFAs promoted significant increase of time-domain measures of HRV, however simvastatin showed a more pronounced positive effect on the temporal and spectral parameters of HRV. The combination of ω‑3 PUFAs and simvastatin in the treatment of patients with T2DM and functional stage of CAN was accompanied by the most pronounced, positive, reliable changes in lipid metabolism, temporal and spectral parameters of HRV. Conclusion. Obtained results of our study could prove the expediency of combined ω‑3 PUFAs and statins prescription to patients with T2DM and functional stage of CAN.

Pdf (Українська)

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