Department of Clinical Nutrition, School of Nutritional Sciences and Dietetics, Tehran University of Medical Sciences, Tehran, Iran.
Diabetes Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran, Iran.
Oxid Med Cell Longev. 2020 Mar 9;2020:5850865. doi: 10.1155/2020/5850865. eCollection 2020.
Lipoprotein-associated phospholipase A (Lp-PLA2) is a new specific vascular inflammation biomarker that is carried by the lipoproteins in the blood and plays a prominent role in the pathogenesis of atherosclerosis. Increased Lp-PLA2 levels and impaired Lp-PLA2 distribution across high-density lipoprotein (HDL) and non-HDL lipoproteins have been reported in diabetic patients, which is associated with the increase in cardiovascular disease (CVD) risk. This study is aimed at investigating the effect of alpha lipoic acid (ALA), as an antioxidant with potential cardioprotective properties, on the Lp-PLA2 mass and its distribution in diabetic patients. In a double-blind, randomized, placebo-controlled clinical trial, seventy diabetic patients were randomly allocated to ALA (1200 mg ALA as two 600 mg capsules/day) and placebo (two maltodextrin capsules/day) groups. The serum levels of total Lp-PLA2 mass, HDL-Lp-PLA2, oxidized low-density lipoproteins (ox-LDL), apolipoprotein A1 (apo A1), lipid profiles, fasting blood sugar (FBS), and insulin were measured, and apolipoprotein B- (apoB-) associated Lp-PLA2 and homeostasis model of assessment index (HOMA-IR) were calculated at the baseline and after 8 weeks of intervention. ALA significantly decreased the ox-LDL, total Lp-PLA2 mass, apoB-associated Lp-PLA2, and percent of apoB-associated Lp-PLA2 and triglyceride and increased the percent of HDL-Lp-PLA2 compared with the placebo group but had no significant effect on HDL-Lp-PLA2 mass, apo A1, lipid profiles, and glycemic indices. There was a positive correlation between the reduction in the ox-LDL level and total Lp-PLA2 mass in the ALA group. In conclusion, ALA may decrease the CVD risk by reducing the ox-LDL and Lp-PLA2 mass and improving the Lp-PLA2 distribution among lipoproteins in type 2 diabetic patients.
脂蛋白相关磷脂酶 A(Lp-PLA2)是一种新型的特异性血管炎症生物标志物,它存在于血液中的脂蛋白中,在动脉粥样硬化的发病机制中起着重要作用。研究报道,糖尿病患者的 Lp-PLA2 水平升高,且 Lp-PLA2 在高密度脂蛋白(HDL)和非高密度脂蛋白脂蛋白中的分布受损,这与心血管疾病(CVD)风险的增加有关。本研究旨在探讨α-硫辛酸(ALA)作为一种具有潜在心脏保护作用的抗氧化剂对糖尿病患者 Lp-PLA2 质量及其分布的影响。在一项双盲、随机、安慰剂对照的临床试验中,将 70 例糖尿病患者随机分为 ALA 组(1200mg ALA 分为 2 次,每次 600mg 胶囊/天)和安慰剂组(2 次麦芽糊精胶囊/天)。在基线和干预 8 周后,测量血清总 Lp-PLA2 质量、HDL-Lp-PLA2、氧化型低密度脂蛋白(ox-LDL)、载脂蛋白 A1(apo A1)、血脂谱、空腹血糖(FBS)和胰岛素,并计算载脂蛋白 B-(apoB-)相关的 Lp-PLA2 和稳态模型评估的胰岛素抵抗指数(HOMA-IR)。与安慰剂组相比,ALA 显著降低了 ox-LDL、总 Lp-PLA2 质量、apoB 相关 Lp-PLA2 和 apoB 相关 Lp-PLA2 的百分比以及甘油三酯,并增加了 HDL-Lp-PLA2 的百分比,但对 HDL-Lp-PLA2 质量、apo A1、血脂谱和血糖指数无显著影响。ALA 组 ox-LDL 水平的降低与总 Lp-PLA2 质量呈正相关。结论:ALA 可通过降低 ox-LDL 和 Lp-PLA2 质量,改善 2 型糖尿病患者脂蛋白中 Lp-PLA2 的分布,从而降低 CVD 风险。