Argeros Zoe, Xu Xiaoye, Bhandari Buna, Harris Katie, Touyz Rhian M, Schutte Aletta E
School of Population Health, University of New South Wales, Sydney, Australia (Z.A., X.X., A.E.S.).
The George Institute for Global Health, Sydney, Australia (X.X., K.H., A.E.S.).
Hypertension. 2025 Nov;82(11):1844-1856. doi: 10.1161/HYPERTENSIONAHA.125.25129. Epub 2025 Sep 26.
There are inconsistent reports regarding the effect of magnesium intake on blood pressure (BP) across hypertensive and normotensive populations.
We performed a meta-analysis and dose-response analysis to explore the relationship between magnesium supplementation and BP in randomized-controlled trials with a duration of ≥4 weeks, using a cubic spline regression model.
Thirty-eight randomized controlled trials involving 2709 participants were eligible for inclusion. Studies included an elemental magnesium dose from 82.3 mg to 637 mg with a median dose of 365 mg and a median intervention period of 12 weeks. Mean differences of changes in BP were calculated by random effects meta-analysis. Magnesium intake resulted in a reduction in systolic BP of -2.81 mm Hg (95% CI, -4.32 to -1.29) and diastolic BP by -2.05 mm Hg (95% CI, -3.23 to -0.88) compared with placebo. Hypertensive individuals on BP-lowering medication and individuals with hypomagnesemia yielded greater systolic BP reductions of -7.68 and -5.97 mm Hg, respectively (<0.05), and diastolic BP reductions of -2.96 and -4.75 mm Hg, respectively (<0.05). In normotensive groups, statistical significance was not reached. We identified high heterogeneity across studies. We found no dose-response relationship between magnesium and BP changes (all ≥0.20).
Our findings support the beneficial effect of magnesium on reducing BP among populations with hypertension and hypomagnesemia, although effects should be interpreted with caution due to high heterogeneity of studies. Larger, well-designed studies assessing higher magnesium doses are needed to refine the dose-response relationship between magnesium intake and BP and identify potential optimal supplementation strategies for subpopulations.
关于镁摄入量对高血压人群和血压正常人群血压的影响,报告结果并不一致。
我们进行了一项荟萃分析和剂量反应分析,以探讨在持续时间≥4周的随机对照试验中,补充镁与血压之间的关系,采用三次样条回归模型。
38项涉及2709名参与者的随机对照试验符合纳入标准。研究中的元素镁剂量为82.3毫克至637毫克,中位剂量为365毫克,中位干预期为12周。通过随机效应荟萃分析计算血压变化的平均差异。与安慰剂相比,镁摄入使收缩压降低了-2.81毫米汞柱(95%置信区间,-4.32至-1.29),舒张压降低了-2.05毫米汞柱(95%置信区间,-3.23至-0.88)。服用降压药物的高血压个体和低镁血症个体的收缩压分别有更大幅度的降低,为-7.68和-5.97毫米汞柱(<0.05),舒张压分别降低-2.96和-4.75毫米汞柱(<0.05)。在血压正常组中,未达到统计学显著性。我们发现各研究之间存在高度异质性。我们未发现镁与血压变化之间存在剂量反应关系(所有P≥0.20)。
我们的研究结果支持镁对高血压人群和低镁血症人群降低血压的有益作用,不过由于研究的高度异质性,对结果的解释应谨慎。需要开展更大规模、设计良好的研究来评估更高镁剂量,以完善镁摄入量与血压之间的剂量反应关系,并确定亚人群潜在的最佳补充策略。