Key result
Combined prescription of simvastatin and w-3 polyunsaturated fatty acids significantly improved the blood lipid spectrum and decreased insulin resistance in patients with T2DM and CAN.
Why the study?
There is currently no unified treatment algorithm for cardiac autonomic neuropathy in patients with type 2 diabetes mellitus.
Does the combination of simvastatin and omega-3 PUFAs improve lipid profiles and insulin resistance in patients with type 2 diabetes mellitus and cardiac autonomic neuropathy?
Does the combination of simvastatin and omega-3 PUFAs improve lipid profiles and insulin resistance in patients with type 2 diabetes mellitus and cardiac autonomic neuropathy?
The combination of simvastatin and omega-3 PUFAs improves lipid profiles and reduces insulin resistance in patients with type 2 diabetes and cardiac autonomic neuropathy.
Introduction. Currently, there is no unified treatment algorithm of cardiac autonomic neuropathy (CAN) in patients with type 2 diabetes mellitus (T2DM). The aim of the study was to investigate the effects of simvastatin (SIM) and w-3 polyunsaturated fatty acids (w-3 PUFAs) on blood lipid profile and insulin resistance (IR) in patients with type 2 diabetes mellitus and definite cardiac autonomic neuropathy. Materials and methods. The study involved 72 patients with T2DM and definite CAN. Patients were divided into four groups: 1st – received standard hypoglycemic therapy – control (n = 15); 2nd (n = 22) – in addition simvastatin (SIM) 20.0 mg/q.d.; 3rd (n = 18) – in addition 1 capsule/q.d. of the ω-3 PUFAs; 4th (n = 17) – in addition SIM 10.0 mg/q.d and 1 capsule/q.d of the ω-3 PUFAs for three months. The concentration of glucose, glycated hemoglobin A1c, immunoreactive insulin (IRI), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), triglycerides (TG) in the blood were determined. Homeostasis model assessment IR (HOMA-IR), atherogenic coefficient (AC), TG/LDL-C, TG/TC, TG/LDL-C and TG and glucose index (TyG) were calculated. Results. Prescription of SIM was accompanied by a statistically significant decrease in TC, LDL-C, TG concentrations. In parallel, SIM induced a decrease of AC, TG/HDL-C, increase in HDL-C, and does not affect the IRI, HOMA-IR, TG/LDL-C, TG/TC, TC/LDL-C/HDL-C, TyG. The use of ω-3 PUFAs has contributed to a significant reduction in TG, AC, TG/LDL-C, TG/TC, TG/HDL-C, TyG index, increase in HDL-C, and was not accompanied by changes in IRI content, HOMA-IR, TC, LDL-C, and TC/LDL-C/HDL-C. The combined prescription of SIM and w-3 PUFAs was accompanied by more pronounced, statistically significant changes in the blood lipid spectrum, as well as a decrease in the IRI and HOMA-IR. Conclusions. Obtained results justify the appropriateness of combined simvastatin and w-3 polyunsaturated fatty acids prescription to patients with type 2 diabetes mellitus and definite cardiac autonomic neuropathy.
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Serhiyenko et al. (2021) studied type 2 diabetes mellitus and definite cardiac autonomic neuropathy (n=72). Simvastatin and w-3 polyunsaturated fatty acids vs. Standard hypoglycemic therapy was evaluated on Blood lipid profile and insulin resistance (IR). Combined prescription of simvastatin and w-3 polyunsaturated fatty acids significantly improved the blood lipid spectrum and decreased insulin resistance in patients with T2DM and CAN.
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