Soohoo Melissa, Feng Mingliang, Obi Yoshitsugu, Streja Elani, Rhee Connie M, Lau Wei Ling, Wang Jialin, Ravel Vanessa A, Brunelli Steven, Kovesdy Csaba P, Kalantar-Zadeh Kamyar
Harold Simmons Center for Kidney Disease Research and Epidemiology, University of California Irvine, School of Medicine, Orange, Calif., USA.
Am J Nephrol. 2016;43(2):85-96. doi: 10.1159/000444890. Epub 2016 Mar 8.
Abnormalities in mineral and bone disorder (MBD) markers are common in patients with chronic kidney disease. However, previous studies have not accounted for their changes over time, and it is unclear whether these changes are associated with survival.
We examined the association of change in MBD markers (serum phosphorus (Phos), albumin-corrected calcium (Ca(Alb)), intact parathyroid hormone (iPTH) and alkaline phosphatase (ALP)) during the first 6 months of hemodialysis (HD) with all-cause mortality across baseline MBD strata using survival models adjusted for clinical characteristics and laboratory measurements in 102,754 incident HD patients treated in a large dialysis organization between 2007 and 2011.
Across all MBD markers (Phos, Ca(Alb), iPTH and ALP), among patients whose baseline MBD levels were higher than the reference range, increase in MBD levels was associated with higher mortality (reference group: MBD level within reference range at baseline and no change at 6 months follow-up). Conversely, decrease in Phos and iPTH, among baseline Phos and iPTH levels lower than the reference range, respectively, were associated with higher mortality. An increase in ALP was associated with higher mortality across baseline strata of ALP ≥80 U/l. However, patients with baseline ALP <80 U/l trended towards a lower risk of mortality irrespective of the direction of change at 6 months follow-up.
There is a differential association between changes in MBD markers with mortality across varying baseline levels in HD patients. Further study is needed to determine if consideration of both baseline and longitudinal changes in the management of MBD derangements improves outcomes in this population.
矿物质和骨代谢紊乱(MBD)标志物异常在慢性肾脏病患者中很常见。然而,既往研究未考虑其随时间的变化,且尚不清楚这些变化是否与生存率相关。
我们在102754例2007年至2011年期间在一个大型透析机构接受治疗的新进入血液透析(HD)患者中,使用根据临床特征和实验室测量值调整的生存模型,研究HD开始后前6个月内MBD标志物(血清磷(Phos)、白蛋白校正钙(Ca(Alb))、全段甲状旁腺激素(iPTH)和碱性磷酸酶(ALP))的变化与全因死亡率之间的关联,该关联根据基线MBD分层进行分析。
在所有MBD标志物(Phos、Ca(Alb)、iPTH和ALP)中,基线MBD水平高于参考范围的患者中,MBD水平升高与较高死亡率相关(参考组:基线时MBD水平在参考范围内且随访6个月时无变化)。相反,基线Phos和iPTH水平分别低于参考范围时,Phos和iPTH降低与较高死亡率相关。在基线ALP≥80 U/l的各分层中,ALP升高与较高死亡率相关。然而,基线ALP<80 U/l的患者,无论随访6个月时变化方向如何,死亡率风险均有降低趋势。
HD患者中,MBD标志物变化与死亡率之间的关联在不同基线水平存在差异。需要进一步研究以确定在MBD紊乱管理中同时考虑基线和纵向变化是否能改善该人群的预后。