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口服镁补充剂与代谢综合征:一项随机、双盲、安慰剂对照的临床试验。

Oral Magnesium Supplementation and Metabolic Syndrome: A Randomized Double-Blind Placebo-Controlled Clinical Trial.

机构信息

Biomedical Research Unit of the Mexican Social Security Institute, Durango, Durango, Mexico; and Research Group on Diabetes and Chronic Illnesses, Durango, Durango, Mexico.

Biomedical Research Unit of the Mexican Social Security Institute, Durango, Durango, Mexico; and Research Group on Diabetes and Chronic Illnesses, Durango, Durango, Mexico.

出版信息

Adv Chronic Kidney Dis. 2018 May;25(3):261-266. doi: 10.1053/j.ackd.2018.02.011.

DOI:10.1053/j.ackd.2018.02.011
PMID:29793665
Abstract

The objective of the study was to evaluate the efficacy of oral magnesium supplementation in the improvement of metabolic syndrome (MetS) and its components. This is a randomized double-blind, placebo-controlled clinical trial that enrolled 198 individuals with MetS and hypomagnesemia who were randomly allocated to receive either 30 mL of magnesium chloride 5% solution, equivalent to 382 mg of elemental magnesium (n = 100), or placebo solution (n = 98), daily for 16 weeks. Serum magnesium levels <1.8 mg/dL defined hypomagnesemia. At final conditions, a total of 48 (48%) and 76 (77.5%) individuals had MetS in the magnesium and placebo groups (P = 0.01), respectively. At baseline, percent of individuals with 3, 4, and 5 criteria of MetS in the magnesium group were 60.0%, 37.0%, and 3.0%, respectively, and in the control group 55.1%, 35.7%, and 9.2%, respectively. Between basal and final conditions, changes in the components of MetS were significantly higher in the magnesium than placebo groups: -3.6 ± 3.3 mmHg, P = 0.001 for systolic blood pressure; -5.5 ± 1.7 mmHg, P = 0.005 for diastolic blood pressure; -12.4 ± 3.6 mg/dL, P < 0.005 for fasting glucose; -61.2 ± 24 mg/dL, P = 0.003 for triglycerides; and 0.9 ± 0.4 mg/dL, P = 0.06 for high-density lipoprotein cholesterol. Magnesium supplementation improves MetS by reducing blood pressure, hyperglycemia, and hypertriglyceridemia.

摘要

本研究旨在评估口服镁补充剂在改善代谢综合征(MetS)及其组成部分方面的疗效。这是一项随机、双盲、安慰剂对照的临床试验,共纳入 198 名伴有低镁血症的 MetS 患者,将其随机分为两组,分别接受 30ml 5%氯化镁溶液(相当于 382mg 元素镁)(n=100)或安慰剂溶液(n=98),每日一次,持续 16 周。血清镁水平<1.8mg/dL 定义为低镁血症。在最终条件下,镁组和安慰剂组分别有 48(48%)和 76(77.5%)名患者患有 MetS(P=0.01)。基线时,镁组有 3、4 和 5 项 MetS 标准的患者比例分别为 60.0%、37.0%和 3.0%,而对照组分别为 55.1%、35.7%和 9.2%。在基线和最终条件之间,镁组代谢综合征各组成部分的变化明显高于安慰剂组:收缩压下降 3.6±3.3mmHg,P=0.001;舒张压下降 5.5±1.7mmHg,P=0.005;空腹血糖下降 12.4±3.6mg/dL,P<0.005;甘油三酯下降 61.2±24mg/dL,P=0.003;高密度脂蛋白胆固醇升高 0.9±0.4mg/dL,P=0.06。镁补充剂通过降低血压、高血糖和高三酰甘油血症来改善 MetS。

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