Division of Nephrology, Department of Internal Medicine, Shin-Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan.
Fu-Jen Catholic University School of Medicine, Taipei, Taiwan.
Med Sci Monit. 2019 Jan 24;25:691-699. doi: 10.12659/MSM.913137.
BACKGROUND Rapid shifting between extracellular and intracellular phosphorus can occur during dialysis sessions, which can cause aberrant intracellular signaling in long-term hemodialysis (LTHD) patients. However, the effect of these intra-dialysis fluctuations of phosphorus on clinical outcomes has not been examined. Therefore, we investigated the relationship between intradialysis serum phosphorus reduction ratio (IDSPRR) and mortality in LTHD patients. MATERIAL AND METHODS This was a retrospective, observational cohort study to assess the predictive power of IDSPRR (>0.63 vs. ≤0.63) on mortality in a total of 805 LTHD patients. All these fatal events were analyzed using the Cox proportional hazards regression model. RESULTS After multivariable analysis, baseline IDSPRR higher than 0.63 was significantly predictive of all-cause mortality (hazard ratio [HR]: 1.58; 95% confidence interval [CI]: 1.10-2.26), but not for cardiovascular (CV) mortality (HR: 1.41; 95% CI: 0.91-2.18). However, when time-varied IDSPRRs were applied, a value greater than 0.63 was not only significantly predictive of all-cause mortality (HR: 1.74, 95% CI: 1.16-2.63), but also CV mortality (HR: 2.04, 95% CI: 1.23-3.40). CONCLUSIONS High IDSPRR (>0.63) is independently associated with increased all-cause and CV mortality, which shows the negative effect of rapid intracellular phosphorus-shifting on LTHD patients.
在透析过程中,细胞外和细胞内磷之间会迅速转换,这可能导致长期血液透析(LTHD)患者出现异常的细胞内信号。然而,这些透析过程中磷的波动对临床结果的影响尚未得到检验。因此,我们研究了 LTHD 患者透析中血清磷降低率(IDSPRR)与死亡率之间的关系。
这是一项回顾性、观察性队列研究,旨在评估 805 例 LTHD 患者中 IDSPRR(>0.63 与≤0.63)对死亡率的预测能力。使用 Cox 比例风险回归模型分析所有这些致死事件。
经过多变量分析,基线 IDSPRR 高于 0.63 与全因死亡率显著相关(危险比[HR]:1.58;95%置信区间[CI]:1.10-2.26),但与心血管(CV)死亡率无关(HR:1.41;95% CI:0.91-2.18)。然而,当应用时变 IDSPRR 时,大于 0.63 的值不仅与全因死亡率显著相关(HR:1.74,95% CI:1.16-2.63),而且与 CV 死亡率相关(HR:2.04,95% CI:1.23-3.40)。
高 IDSPRR(>0.63)与全因和 CV 死亡率增加独立相关,这表明快速细胞内磷转移对 LTHD 患者的负面影响。