Sakaguchi Yusuke, Fujii Naohiko, Shoji Tatsuya, Hayashi Terumasa, Rakugi Hiromi, Iseki Kunitoshi, Tsubakihara Yoshiharu, Isaka Yoshitaka
Geriatric Medicine and Nephrology, Osaka University Graduate School of Medicine, 2-2, Yamada-oka, Suita, Osaka, 565-0871, Japan.
Committee of Renal Data Registry, Japanese Society for Dialysis Therapy, Tokyo, Japan.
PLoS One. 2014 Dec 29;9(12):e116273. doi: 10.1371/journal.pone.0116273. eCollection 2014.
In vitro studies have shown inhibitory effects of magnesium (Mg) on phosphate-induced calcification of vascular smooth muscle cells, raising the possibility that maintaining a high Mg level may be useful for reducing cardiovascular risks of patients with hyperphosphatemia. We examined how serum Mg levels affect the association between serum phosphate levels and the risk of cardiovascular mortality in patients undergoing hemodialysis.
A nationwide register-based cohort study was conducted using database of the Renal Data Registry of the Japanese Society for Dialysis Therapy in 2009. We identified 142,069 patients receiving in-center hemodialysis whose baseline serum Mg and phosphate levels were available. Study outcomes were one-year cardiovascular and all-cause mortality. Serum Mg levels were categorized into three groups (lower, <2.7 mg/dL; intermediate, ≥2.7, <3.1 mg/dL; and higher, ≥3.1 mg/dL).
During follow-up, 11,401 deaths occurred, out of which 4,751 (41.7%) were ascribed to cardiovascular disease. In multivariable analyses, an increase in serum phosphate levels elevated the risk of cardiovascular mortality in the lower- and intermediate-Mg groups, whereas no significant risk increment was observed in the higher-Mg group. Moreover, among patients with serum phosphate levels of ≥6.0 mg/dL, the cardiovascular mortality risk significantly decreased with increasing serum Mg levels (adjusted odds ratios [95% confidence intervals] of the lower-, intermediate-, and higher-Mg groups were 1.00 (reference), 0.81 [0.66-0.99], and 0.74 [0.56-0.97], respectively.). An interaction between Mg and phosphate on the risk of cardiovascular mortality was statistically significant (P = 0.03).
Serum Mg levels significantly modified the mortality risk associated with hyperphosphatemia in patients undergoing hemodialysis.
体外研究表明,镁(Mg)对磷酸盐诱导的血管平滑肌细胞钙化具有抑制作用,这增加了维持高镁水平可能有助于降低高磷血症患者心血管风险的可能性。我们研究了血清镁水平如何影响接受血液透析患者的血清磷水平与心血管死亡风险之间的关联。
2009年,利用日本透析治疗学会肾脏数据登记处的数据库进行了一项基于全国登记的队列研究。我们确定了142,069名接受中心血液透析且可获得基线血清镁和磷水平的患者。研究结局为一年内心血管死亡率和全因死亡率。血清镁水平分为三组(低水平,<2.7mg/dL;中等水平,≥2.7,<3.1mg/dL;高水平,≥3.1mg/dL)。
随访期间,共发生11,401例死亡,其中4,751例(41.7%)归因于心血管疾病。在多变量分析中,血清磷水平升高增加了低镁和中等镁组的心血管死亡风险,而在高镁组中未观察到显著的风险增加。此外,在血清磷水平≥6.0mg/dL的患者中,心血管死亡风险随着血清镁水平的升高而显著降低(低镁、中等镁和高镁组的调整优势比[95%置信区间]分别为1.00(参照)、0.81[0.66 - 0.99]和0.74[0.56 - 0.97])。镁和磷对心血管死亡风险的相互作用具有统计学意义(P = 0.03)。
血清镁水平显著改变了接受血液透析患者高磷血症相关的死亡风险。