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Combined Alkaline Phosphatase and Phosphorus Levels as a Predictor of Mortality in Maintenance Hemodialysis Patients

机译:碱性磷酸酶和磷水平联合作为维持性血液透析患者死亡率的预测指标

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Abstract: Hyperphosphatemia-induced vascular calcification and higher alkaline phosphatase (ALP) levels-related high-turnover bone diseases are linked to mortality among patients with chronic kidney disease (CKD). Nonetheless, no large epidemiological study in patients with CKD has been conducted to investigate the interaction and joint effect of hyperphosphatemia and higher ALP levels on mortality. We analyzed 11,912 maintenance hemodialysis patients from January 2005 to December 2010. Unadjusted and adjusted hazard ratios (aHRs) of death were calculated for different categories of serum phosphorus and ALP using the Cox regression model. The modification effect between serum phosphorus and ALP on mortality was determined using an interaction product term. Both hypophosphatemia (7.0?mg/dL) were associated with incremental risks of death (aHR: 1.25 [95% confidence intervals (CIs): 1.09–1.44], and 1.15 [95% CI: 1.01–1.31], respectively) compared to the lowest hazard ratio (HR) group (5?mg/dL?≤?phosphorus??150?U/L). In the stratified analysis, patients with combined higher ALP (>150?U/L) and hyperphosphatemia (>7.0?mg/dL) had the greatest mortality risk (aHR: 2.25 [95% CI: 1.69–2.98] compared to the lowest HR group (ALP?≤?60?U/L and 4?mg/dL?≤?phosphorus?P?=?0.22). The association between serum phosphorus levels and mortality was not limited to higher ALP levels. Regardless of serum ALP levels, we may control serum phosphorus levels merely toward the normal range. While considering the joint effect of ALP and hyperphosphatemia on mortality, the optimal phosphorus range should be stricter.
机译:摘要:高磷血症引起的血管钙化和高碱性磷酸酶(ALP)水平相关的高周转性骨病与慢性肾脏病(CKD)患者的死亡率有关。但是,尚未对CKD患者进行大规模的流行病学研究,以研究高磷血症和较高的ALP水平对死亡率的相互作用和联合作用。我们分析了2005年1月至2010年12月的11,912例维持性血液透析患者。使用Cox回归模型计算了不同类别的血清磷和ALP的未调整和调整的死亡风险比(aHRs)。使用相互作用乘积项确定血清磷和ALP对死亡率的修饰作用。两种低磷血症(7.0?mg / dL)均与死亡的增加风险相关(aHR:1.25 [95%置信区间(CIs):1.09–1.44]和1.15 [95%CI:1.01–1.31])最低危险比(HR)组(5?mg / dL?≤?磷?? 150?U / L)。在分层分析中,合并较高的ALP(> 150?U / L)和高磷酸盐血症(> 7.0?mg / dL)的患者死亡风险最高(aHR:2.25 [95%CI:1.69–2.98],而最低者HR组(ALP≤60U/ L和4mg /dL≤P<0.22),血清磷水平与死亡率之间的关系不限于较高的ALP水平,而与血清ALP无关血清磷水平只能控制在正常范围内,在考虑ALP和高磷血症对死亡率的联合影响时,最佳磷范围应更严格。

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