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Circulating CD5L is associated with cardiovascular events and all-cause mortality in individuals with chronic kidney
Esmeralda Castelblanco1,2,3, Maria R Sarrias4, Àngels Betriu5
1Department of Endocrinology and Nutrition, Hospital de la Santa Creu i Sant Pau and Sant Pau Biomedical Research Institute (IIB Sant Pau), Barcelona 08041, Spain.
Insights
Higher CD5L levels increase cardiovascular event and mortality risk in chronic kidney disease (CKD) patients. Soluble CD36 (sCD36) showed no significant association with these adverse outcomes.
Area of Science:
- Nephrology
- Cardiology
- Biomarkers
Background:
- Cardiovascular disease (CVD) is a leading cause of mortality in patients with chronic kidney disease (CKD).
- Identifying novel biomarkers for cardiovascular event (CVE) risk stratification in CKD is crucial.
Purpose of the Study:
- To investigate the association of CD5L and soluble CD36 (sCD36) with the risk of CVE and all-cause mortality in individuals with CKD.
Main Methods:
- Prospective cohort study of 1,516 participants with CKD, free from pre-existing CVD.
- Cox proportional hazards regression was used to analyze the association of baseline CD5L and sCD36 with a composite CVE endpoint and all-cause mortality, adjusted for established CV risk factors.
- Follow-up duration was 4 years.
Main Results:
- Higher baseline CD5L concentrations were significantly associated with an increased risk of CVE (HR: 1.17, 95% CI: 1.0-1.36) and all-cause mortality (HR: 1.22, 95% CI: 1.01-1.48) after multivariable adjustment.
- No significant association was found between sCD36 levels and adverse cardiovascular outcomes or mortality.
- The study included 98 CVEs and 72 deaths (26 CV-related) over 4 years.
Conclusions:
- Elevated CD5L concentrations represent a novel, independent risk factor for future cardiovascular events and all-cause mortality in individuals with CKD.
- CD5L may serve as a potential biomarker for risk prediction in this high-risk population.
- sCD36 does not appear to be associated with cardiovascular risk in CKD.
Abstract:
This study assessed the association of CD5L and soluble CD36 (sCD36) with the risk of a cardiovascular event (CVE), including CV death and all-cause mortality in CKD. We evaluated the association of CD5L and sCD36 with a predefined composite CV endpoint (unstable angina, myocardial infarction, transient ischemic attack, cerebrovascular accident, congestive heart failure, arrhythmia, peripheral arterial disease [PAD] or amputation by PAD, aortic aneurysm, or death from CV causes) and all-cause mortality using Cox proportional hazards regression, adjusted for CV risk factors. The analysis included 1,516 participants free from pre-existing CV disease followed up for 4 years. The median age was 62 years, 38.8% were female, and 26.8% had diabetes. There were 98 (6.5%) CVEs and 72 (4.8%) deaths, of which 26 (36.1%) were of CV origin. Higher baseline CD5L concentration was associated with increased risk of CVE (HR, 95% CI, 1.17, 1.0-1.36), and all-cause mortality (1.22, 1.01-1.48) after adjusting for age, sex, diabetes, systolic blood pressure, dyslipidemia, waist circumference, smoking, and CKD stage. sCD36 showed no association with adverse CV outcomes or mortality. Our study showed for the first time that higher concentrations of CD5L are associated with future CVE and all-cause mortality in individuals with CKD.
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