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Homocitrulline Is Associated with Cardiovascular Outcomes in Nondialysis Patients with CKD
Solène M Laville1,2, Stéphane Jaisson3, Philippe Gillery3
1MP3CV Laboratory, Jules Verne University of Picardie, Amiens, France.
Insights
Higher homocitrulline (HCit) levels in chronic kidney disease (CKD) patients are linked to increased cardiovascular events and mortality. This study highlights HCit as a potential biomarker for adverse outcomes in CKD.
Area of Science:
- Nephrology
- Cardiovascular Medicine
- Biochemistry
Background:
- Protein carbamylation, indicated by homocitrulline (HCit), elevates cardiovascular risk, particularly in chronic kidney disease (CKD) patients with high urea.
- HCit serves as a biomarker for overall protein carbamylation.
Purpose of the Study:
- To investigate the association between serum HCit concentration and adverse cardiovascular outcomes and all-cause mortality in non-dialysis CKD patients.
- To determine if HCit levels predict major adverse cardiovascular events (MACE) and death before kidney replacement therapy (KRT).
Main Methods:
- A prospective cohort study (CKD-REIN) included 2,195 CKD patients (eGFR <60mL/min/1.73m2).
- Serum HCit was measured at baseline and patients were grouped into tertiles.
- Adjusted Cox proportional hazards models analyzed risks for MACE and death before KRT.
Main Results:
- Serum HCit concentration correlated with decreased eGFR and increased urea levels.
- Higher HCit tertiles (T2 and T3) were independently associated with increased risk of MACE compared to the lowest tertile (T1).
- Elevated HCit levels significantly increased the risk of death before KRT.
Conclusions:
- Serum HCit concentration is associated with a higher likelihood of MACE and death in CKD patients.
- Further research into therapeutic interventions to reduce carbamylation is warranted to confirm causality.
No abstract available in PubMed .
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