Effect of Levocarnitine on Physical and Biochemical Parameters in Patients with Polycystic Ovary Syndrome

Kazi Shamim Ara, F. Deeba, Shakeela Ishrat, Mitu Debnath, Farhana Karim Satu, F. Chowdhury
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Abstract

Background: Polycystic ovary syndrome (PCOS) is a common disorder in women of reproductive age closely related to insulin resistance, obesity, dyslipidaemia and long term diseases including diabetes and cardiovascular disease. The management of PCOS may be challenging on account of the comorbidities associated with the disease. Objective: The objective of the study was to evaluate the effect of Levocarnitine supplementation on physical and biochemical parameters in polycystic ovary syndrome. Methods: This randomized controlled study was conducted in the Department of Reproductive Endocrinology and Infertility, Bangabandhu Sheikh Mujib Medical University, Dhaka from January 2021 to December 2021. Total 78 diagnosed cases of PCOS were selected for medication and were included in this study. Eligible women who gave their informed consent were allocated into either Group A (Levocarnitine) or Group B (Placebo) on the basis of computer generated table. Group A received Levocarnitine and Group B received Placebo for 12 weeks. Then pretreatment and post treatment physical parameters including BMI, waist circumference and biochemical parameters including cholesterol, triglyceride, LDL, HDL, fasting plasma glucose, fasting insulin, HOMA-IR were assessed. Results: Treatment with levocarnitine significantly reduced BMI (-6.00±0.00 vs -0.45±0.07) waist circumference (-4.88±2.85 vs -0.77±0.30) compared with the placebo. In Levocarnitine group, total cholesterol (-38.15±7.33 vs -0.79±27.00 mg/dl), serum triglycerides (-60.00±53.33 vs. -0.33±9.59 mg/d) and LDL (-23.49±1.81 vs. -0.41±0.07 mg/dl) were significantly reduced and HDL level was significantly increased (4.23±1.62 vs 0.41±0.49 mg/dl) compared with the placebo group. Moreover, compared with the placebo, levocarnitine led to a significant reduction of fasting plasma glucose, fasting insulin and HOMA-IR (-0.49±0.95 vs. 0.09± 0.29). Conclusion: In conclusion, levocarnitine administration led to an improvement in physical parameters including BMI, waist circumference as well as biochemical factors including cholesterol, triglyceride, LDL, HDL. Insulin resistance was significantly reduced in post treatment patients of Levocarnitine. In contrast, although physical and biochemical parameters improved in the placebo group, the change was not significant.
左卡尼汀对多囊卵巢综合征患者生理生化指标的影响
背景:多囊卵巢综合征(PCOS)是育龄妇女常见病,与胰岛素抵抗、肥胖、血脂异常及糖尿病、心血管疾病等长期疾病密切相关。多囊卵巢综合征的管理可能是具有挑战性的,因为与疾病相关的合并症。目的:探讨补充左卡尼汀对多囊卵巢综合征患者生理生化指标的影响。方法:本随机对照研究于2021年1月至2021年12月在达卡Bangabandhu Sheikh Mujib医科大学生殖内分泌与不孕症学系进行。本研究共选取78例诊断为多囊卵巢综合征的患者进行药物治疗。给予知情同意的符合条件的妇女根据计算机生成的表格被分配到A组(左卡尼汀)或B组(安慰剂)。A组给予左卡尼汀治疗,B组给予安慰剂治疗,疗程12周。然后评估治疗前和治疗后的身体参数包括BMI、腰围和生化参数包括胆固醇、甘油三酯、LDL、HDL、空腹血糖、空腹胰岛素、HOMA-IR。结果:与安慰剂相比,左卡尼汀治疗显著降低BMI(-6.00±0.00 vs -0.45±0.07)和腰围(-4.88±2.85 vs -0.77±0.30)。左卡尼汀组与安慰剂组相比,总胆固醇(-38.15±7.33 vs -0.79±27.00 mg/dl)、血清甘油三酯(-60.00±53.33 vs -0.33±9.59 mg/d)、低密度脂蛋白(-23.49±1.81 vs -0.41±0.07 mg/dl)水平显著降低,HDL水平显著升高(4.23±1.62 vs 0.41±0.49 mg/dl)。此外,与安慰剂相比,左卡尼汀导致空腹血糖、空腹胰岛素和HOMA-IR显著降低(-0.49±0.95 vs. 0.09±0.29)。结论:左卡尼汀可改善BMI、腰围等生理指标及胆固醇、甘油三酯、LDL、HDL等生化指标。左卡尼汀治疗后胰岛素抵抗明显降低。相比之下,虽然安慰剂组的物理和生化参数有所改善,但变化并不显著。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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