Soluble CD59 in peritoneal dialysis: a potential biomarker for peritoneal membrane function.
Soluble CD59 in peritoneal dialysis: a potential biomarker for peritoneal membrane function.
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DOI:
10.1007/s40620-020-00934-7
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发表时间:
2021-06
影响因子:
3.4
通讯作者:
Poppelaars F
中科院分区:
文献类型:
--
作者:
Faria B;Gaya da Costa M;Lima C;Willems L;Brandwijk R;Berger SP;Daha MR;Pestana M;Seelen MA;Poppelaars F
Various studies have reported the importance of complement regulators in preventing mesothelial damage during peritoneal dialysis (PD). Its assessment, however, is limited in clinical practice due to the lack of easy access to the peritoneal membrane. Recently, a soluble form of the complement regulatory protein CD59 (sCD59) has been described. We therefore aimed to investigate the role of sCD59 in PD. Plasma sCD59 was measured in 48 PD patients, 41 hemodialysis patients, 15 non-dialysis patients with chronic kidney disease and 14 healthy controls by ELISA (Hycult; HK374-02). Additionally, sCD59 and sC5b-9 were assessed in the peritoneal dialysate. sCD59 and sC5b-9 were detectable in the peritoneal dialysate of all patients, and marginally correlated (r = 0.27, P = 0.06). Plasma sCD59 levels were significantly higher in PD patients than in patients with chronic kidney disease and healthy controls, but did not differ from hemodialysis patients. During follow-up, 19% of PD patients developed peritoneal membrane failure and 27% of PD patients developed loss of residual renal function. In adjusted models, increased sCD59 levels in the dialysate (HR 3.44, 95% CI 1.04–11.40, P = 0.04) and in plasma (HR 1.08, 95% CI 1.01–1.17, P = 0.04) were independently associated with the occurrence of peritoneal membrane failure. Higher plasma levels of sCD59 were also associated with loss of residual renal function (HR 1.10, 95% CI 1.04–1.17, P < 0.001). Our study suggests that sCD59 has potential as a biomarker to predict peritoneal membrane function and loss of residual renal function in PD, thereby offering a tool to improve patient management. The online version contains supplementary material available at 10.1007/s40620-020-00934-7.
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影响因子:
7.3
作者:
Faria, Bernardo;da Costa, Mariana Gaya;Seelen, Marc A.
通讯作者:
Seelen, Marc A.
影响因子:
15.9
作者:
Brasoveanu, LI;Fonsatti, E;Maio, M
通讯作者:
Maio, M
影响因子:
12.8
作者:
Qin, Xuebin;Hu, Weiguo;Song, Wenping;Grubissich, Luciano;Hu, Xuemei;Wu, Gongxiong;Ferris, Sean;Dobarro, Martin;Halperin, Jose A.
通讯作者:
Halperin, Jose A.
影响因子:
7.4
作者:
Poppelaars F;Gaya da Costa M;Berger SP;Assa S;Meter-Arkema AH;Daha MR;van Son WJ;Franssen CF;Seelen MA
通讯作者:
Seelen MA
影响因子:
6.1
作者:
Chung, SH;Heimbürger, O;Lindholm, B
通讯作者:
Lindholm, B