Department of Nephrology, Gülhane School of Medicine, Ankara, Turkey.
Am J Nephrol. 2012;36(3):228-37. doi: 10.1159/000341868. Epub 2012 Aug 30.
BACKGROUND: Magnesium is an essential ion for all living cells because over 300 enzymes require the presence of magnesium for their catalytic action. To date, no group has evaluated magnesium as a cardiovascular risk factor in chronic kidney disease (CKD) subjects, in which closely interrelated factors and potential confounders such as endothelial dysfunction, insulin resistance (the homeostasis model assessment (HOMA) index) and inflammation (expressed as serum C-reactive protein (CRP) levels) were also considered. METHODS: Between March 2006 and December 2010, 283 CKD patients were followed up for time-to-event analysis until the occurrence of fatal or nonfatal cardiovascular events. Endothelium-dependent vasodilatation (flow-mediated dilatation; FMD) and endothelium-independent vasodilatation (nitroglycerin-mediated dilatation) of the brachial artery were assessed noninvasively using high-resolution ultrasound. RESULTS: From the univariate analysis of FMD, it appears that a higher magnesium level is associated with less endothelial dysfunction. When a multivariate analysis was performed, magnesium and estimated glomerular filtration rates (eGFR) maintained a strong positive correlation with FMD, supporting the hypothesis that higher levels of magnesium may protect against endothelial damage. In univariate Cox proportional hazards models, FMD, magnesium, high sensitivity CRP, the HOMA index, eGFR, comorbid diabetes, hypertension, smoking status, systolic blood pressure, serum phosphate and intact parathormone emerged as significant predictors for cardiovascular outcomes. Kaplan-Meier curves showed significantly higher cardiovascular mortality rates in CKD patients whose serum magnesium levels were below 2.05 mg/dl. CONCLUSIONS: This observational cohort study showed that magnesium may be an independent predictor of future cardiovascular outcomes and is the first study demonstrating such a role in etiologically diagnosed CKD patients, across different stages.
背景:镁是所有活细胞必需的离子,因为超过 300 种酶需要镁的存在才能发挥其催化作用。迄今为止,尚无任何研究组评估过镁是否为慢性肾脏病(CKD)患者的心血管风险因素,而内皮功能障碍、胰岛素抵抗(稳态模型评估(HOMA)指数)和炎症(以血清 C 反应蛋白(CRP)水平表示)等密切相关的因素和潜在的混杂因素也在该类患者中存在。
方法:2006 年 3 月至 2010 年 12 月,对 283 例 CKD 患者进行了随访,进行时间事件分析,直至发生致命或非致命性心血管事件。肱动脉内皮依赖性血管舒张(血流介导的舒张;FMD)和内皮非依赖性血管舒张(硝酸甘油介导的舒张)采用高分辨率超声进行无创评估。
结果:FMD 的单变量分析表明,较高的镁水平与较低的内皮功能障碍相关。进行多变量分析时,镁和估计肾小球滤过率(eGFR)与 FMD 保持强烈的正相关,支持较高的镁水平可能有助于保护内皮免受损伤的假说。在单变量 Cox 比例风险模型中,FMD、镁、高敏 CRP、HOMA 指数、eGFR、合并糖尿病、高血压、吸烟状况、收缩压、血清磷酸盐和完整甲状旁腺激素均为心血管结局的显著预测因子。Kaplan-Meier 曲线显示,血清镁水平低于 2.05mg/dl 的 CKD 患者的心血管死亡率显著较高。
结论:本观察性队列研究表明,镁可能是未来心血管结局的独立预测因子,并且是第一个在不同阶段病因诊断为 CKD 的患者中证明这一作用的研究。
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