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Protein carbamylation predicts mortality in ESRD.

Abstract
Traditional risk factors fail to explain the increased risk for cardiovascular morbidity and mortality in ESRD. Cyanate, a reactive electrophilic species in equilibrium with urea, posttranslationally modifies proteins through a process called carbamylation, which promotes atherosclerosis. The plasma level of protein-bound homocitrulline (PBHCit), which results from carbamylation, predicts major adverse cardiac events in patients with normal renal function, but whether this relationship is similar in ESRD is unknown. We quantified serum PBHCit in a cohort of 347 patients undergoing maintenance hemodialysis with 5 years of follow-up. Kaplan-Meier analyses revealed a significant association between elevated PBHCit and death (log-rank P<0.01). After adjustment for patient characteristics, laboratory values, and comorbid conditions, the risk for death among patients with PBHCit values in the highest tertile was more than double the risk among patients with values in the middle tertile (adjusted hazard ratio [HR], 2.4; 95% confidence interval [CI], 1.5-3.9) or the lowest tertile (adjusted HR, 2.3; 95% CI, 1.5-3.7). Including PBHCit significantly improved the multivariable model, with a net reclassification index of 14% (P<0.01). In summary, serum PBHCit, a footprint of protein carbamylation, predicts increased cardiovascular risk in patients with ESRD, supporting a mechanistic link among uremia, inflammation, and atherosclerosis.
AuthorsRobert A Koeth, Kamyar Kalantar-Zadeh, Zeneng Wang, Xiaoming Fu, W H Wilson Tang, Stanley L Hazen
JournalJournal of the American Society of Nephrology : JASN (J Am Soc Nephrol) Vol. 24 Issue 5 Pg. 853-61 (Apr 2013) ISSN: 1533-3450 [Electronic] United States
PMID23431074 (Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
Chemical References
  • Proteins
  • homocitrulline
  • Citrulline
Topics
  • Adult
  • Aged
  • Atherosclerosis (etiology)
  • Citrulline (analogs & derivatives, blood)
  • Cohort Studies
  • Female
  • Humans
  • Kidney Failure, Chronic (complications, metabolism, mortality)
  • Male
  • Middle Aged
  • Prognosis
  • Protein Binding
  • Protein Processing, Post-Translational
  • Proteins (metabolism)
  • Renal Dialysis

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