Division of Nephrology, Department of Medicine, University of Tennessee Health Science Center, Memphis, TN, USA.
Nephrology Center, Toranomon Hospital Kajigaya, Kanagawa, Japan.
Nephrol Dial Transplant. 2018 Feb 1;33(2):264-273. doi: 10.1093/ndt/gfw412.
Higher serum alkaline phosphatase (ALP) levels have been associated with excess mortality in patients with non-dialysis-dependent chronic kidney disease (NDD-CKD) and end-stage renal disease (ESRD). However, little is known about the impact of late-stage NDD-CKD ALP levels on outcomes after dialysis initiation.
Among 17 732 US veterans who transitioned to dialysis between October 2007 and September 2011, we examined the association of serum ALP levels averaged over the last 6 months of the pre-ESRD transition period ('prelude period') with all-cause, cardiovascular and infection-related mortality following dialysis initiation, using Cox (for all-cause mortality) and competing risk (for cause-specific mortality) regressions adjusted for demographics, comorbidities, medications, estimated glomerular filtration rate and serum albumin levels over the 6-month prelude period, and vascular access type at dialysis initiation.
During a median follow-up of 2.0 (interquartile range, 1.1-3.2) years following dialysis initiation, a total of 9196 all-cause deaths occurred. Higher ALP levels were incrementally associated with higher all-cause, cardiovascular and infection-related mortality. Compared with patients in the lowest ALP quartile (<66.0 U/L), those in the highest quartile (≥111.1 U/L) had multivariable-adjusted hazard/subhazard ratios (95% confidence interval) of 1.42 (1.34-1.51), 1.43 (1.09-1.88) and 1.39 (1.09-1.78) for all-cause, cardiovascular and infection-related mortality, respectively. The associations remained consistent in various subgroups and after further adjustment for liver enzymes, serum phosphorus and intact parathyroid hormone levels.
Higher pre-ESRD serum ALP levels are independently associated with higher post-ESRD mortality risk. Further studies are warranted to determine if interventions that lower pre-ESRD ALP levels reduce mortality in incident dialysis patients.
血清碱性磷酸酶(ALP)水平升高与非透析依赖性慢性肾脏病(NDD-CKD)和终末期肾病(ESRD)患者的超额死亡率相关。然而,对于晚期 NDD-CKD 患者 ALP 水平对透析开始后结局的影响知之甚少。
在 2007 年 10 月至 2011 年 9 月期间转为透析的 17732 名美国退伍军人中,我们检查了 ESRD 过渡期前 6 个月内血清 ALP 水平的平均值(“前奏期”)与透析开始后全因、心血管和感染相关死亡率之间的关系,使用 Cox(用于全因死亡率)和竞争风险(用于特定原因死亡率)回归,调整了前奏曲期间 6 个月的人口统计学、合并症、药物、估计肾小球滤过率和血清白蛋白水平,以及透析开始时的血管通路类型。
在透析开始后中位数为 2.0(四分位距,1.1-3.2)年的中位随访期间,共发生 9196 例全因死亡。ALP 水平越高,全因、心血管和感染相关死亡率越高。与 ALP 最低四分位数(<66.0U/L)的患者相比,最高四分位数(≥111.1U/L)的患者全因、心血管和感染相关死亡的多变量调整后的危险/亚危险比(95%置信区间)分别为 1.42(1.34-1.51)、1.43(1.09-1.88)和 1.39(1.09-1.78)。这些关联在各种亚组中仍然一致,并且在进一步调整肝酶、血清磷和完整甲状旁腺激素水平后仍然一致。
ESRD 前血清 ALP 水平升高与 ESRD 后死亡率风险增加独立相关。需要进一步研究以确定降低 ESRD 前 ALP 水平是否会降低新透析患者的死亡率。