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

机译:联合碱性磷酸酶和磷水平作为维持性血液透析患者死亡率的预测指标

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摘要

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 (<3.0 mg/dL) and hyperphosphatemia (>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 < 6 mg/dL). ALP levels were linearly associated with incremental risks for death (aHR: 1.58 [95% CI: 1.41–1.76] for the category of ALP > 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 < 5 mg/dL). Although the effect of hyperphosphatemia on mortality seemed stronger in higher ALP levels, the interaction was not statistically significant (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:高磷血症引起的血管钙化和较高水平的碱性磷酸酶(ALP)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,尚未开展关于CKD患者的大规模流行病学研究,以研究高磷血症和更高的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。未经调整和调整的危险比(aHRs)使用Cox回归模型计算了不同类别的血清磷和ALP的死亡率。血清磷和ALP对死亡率的修饰作用是通过相互作用乘积项确定的。低磷血症(<3.0 mg / dL)和高磷血症(> 7.0 mg / dL)均与死亡风险增加相关(aHR:1.25 [95%置信区间(CIs):1.09–1.44]和1.15 [95%CI:1.01–1.31],与最低危险比(HR)组(5μmg/dL≤≤磷<6μmg/ dL)相比。 ALP水平与死亡的增加风险线性相关(对于ALP> 150 U / L,aHR:1.58 [95%CI:1.41-1.76])。在分层分析中,与最低HR组相比,合并较高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] (ALP≤60 U / L和4 mg / dL≤磷 5 mg / dL)。高磷血症对死亡率的影响似乎在较高的ALP水平下更强,但相互作用无统计学意义(P = 0.22)。血清磷水平和死亡率并不限于较高的ALP水平,无论血清ALP水平如何,我们都可以将血清磷水平控制在正常范围内,在考虑ALP和高磷血症对死亡率的联合影响时,最佳磷水平应更严格。

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