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Homocitrulline as marker of protein carbamylation in hemodialyzed patients.

Authors :
Jaisson, Stéphane
Kazes, Isabelle
Desmons, Aurore
Fadel, Fouad
Oudart, Jean-Baptiste
Santos-Weiss, Izabella C.R. Dos
Millart, Hervé
Touré, Fatouma
Rieu, Philippe
Gillery, Philippe
Source :
Clinica Chimica Acta. Sep2016, Vol. 460, p5-10. 6p.
Publication Year :
2016

Abstract

Background Homocitrulline (HCit) is a carbamylation-derived product (CDP) that has been identified as a valuable biomarker of morbidity and mortality in patients with chronic kidney disease (CKD). The aim of this study was to determine whether initiation of hemodialysis therapy (HD) could induce variations of HCit concentrations in CKD patients. Methods Serum HCit concentrations were determined by LC-MS/MS in CKD patients (n = 108) just before (M0) and six months (M6) after the initiation of HD therapy. Results Mean HCit concentrations reached 1000 μmol/mol Lysine before initiation of HD therapy and decreased by 50% within 6 months after HD onset. HCit concentrations remained stable over time as assessed during a 24-months follow-up period. HCit was mostly found in its protein-bound form in HD patients. HCit concentrations obtained at M0 were positively correlated with urea (r = 0.58) and carbamylated hemoglobin (r = 0.41), and are likely to be promising predictive markers of mortality. However, no correlations were found between HCit concentrations and Kt/V values, suggesting that HCit is not a marker of HD efficiency. Conclusion HCit concentrations reflect the intensity of protein carbamylation and are stable over time during HD treatment, making HCit a reliable biomarker in the follow-up of CKD patients. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00098981
Volume :
460
Database :
Academic Search Index
Journal :
Clinica Chimica Acta
Publication Type :
Academic Journal
Accession number :
117267669
Full Text :
https://doi.org/10.1016/j.cca.2016.06.009