Soluble CD59 in peritoneal dialysis: a potential biomarker for peritoneal membrane function.


Journal

Journal of nephrology
ISSN: 1724-6059
Titre abrégé: J Nephrol
Pays: Italy
ID NLM: 9012268

Informations de publication

Date de publication:
06 2021
Historique:
received: 21 08 2020
accepted: 19 11 2020
pubmed: 12 12 2020
medline: 19 8 2021
entrez: 11 12 2020
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 33306183
doi: 10.1007/s40620-020-00934-7
pii: 10.1007/s40620-020-00934-7
pmc: PMC8192357
doi:

Substances chimiques

Biomarkers 0
CD59 Antigens 0
Dialysis Solutions 0
CD59 protein, human 101754-01-2
Complement System Proteins 9007-36-7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

801-810

Références

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Auteurs

Bernardo Faria (B)

Department of Internal Medicine, Division of Nephrology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands. faria_bernardo@yahoo.com.
Nephrology and Infectious Disease R&D Group, INEB, Institute of Investigation and Innovation in Health (i3S), University of Porto, Al. Professor Hernâni Monteiro, 4200-319, Porto, Portugal. faria_bernardo@yahoo.com.

Mariana Gaya da Costa (M)

Department of Internal Medicine, Division of Nephrology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Carla Lima (C)

Hospital São Teotônio, Viseu, Portugal.

Loek Willems (L)

Hycult Biotech, Uden, The Netherlands.

Ricardo Brandwijk (R)

Hycult Biotech, Uden, The Netherlands.

Stefan P Berger (SP)

Department of Internal Medicine, Division of Nephrology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Mohamed R Daha (MR)

Department of Internal Medicine, Division of Nephrology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Department of Nephrology, University of Leiden, Leiden University Medical Center, Leiden, The Netherlands.

Manuel Pestana (M)

Nephrology and Infectious Disease R&D Group, INEB, Institute of Investigation and Innovation in Health (i3S), University of Porto, Al. Professor Hernâni Monteiro, 4200-319, Porto, Portugal.

Marc A Seelen (MA)

Department of Internal Medicine, Division of Nephrology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

Felix Poppelaars (F)

Department of Internal Medicine, Division of Nephrology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.

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