Key result
Novel biomarkers fail to outperform traditional risk factors for predicting cardiovascular mortality in dialysis.
Why the study?
Do adipokines, myokines, gut-microbiota-derived uremic toxins, and nutritional status predict two-year cardiovascular mortality in dialysis patients?
Cohort (n=128)
Do adipokines, myokines, gut-microbiota-derived uremic toxins, and nutritional status predict two-year cardiovascular mortality in dialysis patients?
In dialysis patients, traditional risk factors and inflammatory markers remain stronger predictors of cardiovascular mortality than novel adipokines, myokines, or gut-derived uremic toxins.
Patients with chronic kidney disease (CKD) are at a significantly increased risk of cardiovascular (CV) mortality, which cannot be fully accounted for by traditional risk factors. Background/Objectives: The aim of this study is to evaluate the impact of adipokines, myokines, gut-microbiota-derived uremic toxins, and nutritional status on the risk of CV mortality in patients undergoing kidney replacement therapy (KRT). Methods: This study includes 84 hemodialysis (HD) patients and 44 peritoneal dialysis (PD) patients. Adipokines and myokines concentrations were measured using enzyme-linked immunosorbent assays (ELISA), while gut-microbiota-derived uremic toxins were quantified using liquid chromatography-tandem mass spectrometry (LC–MS/MS). Nutritional status was assessed using the seven-point Subjective Global Assessment (SGA) and anthropometric measurements. The survival was analyzed using Kaplan–Meier curves with the log-rank test, along with univariate and multivariate Cox proportional hazards regression. Results: The mean follow-up period was 18.2 (8) months for the HD group and 14.3 (8) months for the PD group. During the 2-year follow-up, 15.5% of HD patients and 6.8% of PD patients died due to cardiovascular disease (CVD). In the HD group, age, blood urea nitrogen (BUN), phosphorus, interleukin-6 (IL-6), high-sensitivity C-protein (hsCRP), and neutrophil-to-lymphocyte ratio (NLR) levels were significantly associated with CV mortality. HD patients who died had significantly lower myostatin/IL-6 ratios. CV mortality was significantly associated with age and potassium levels in the PD group. Conclusions: The examined adipokines, myokines, and gut-microbiota-derived uremic toxins exert a less significant direct influence on survival compared to widely recognized indicators, including age, nutritional status, and inflammatory markers.
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Czaja-Stolc et al. (2025) conducted a cohort in Chronic kidney disease on kidney replacement therapy (n=128). Adipokines, myokines, gut-microbiota-derived uremic toxins, and nutritional status was evaluated on Cardiovascular mortality. Novel biomarkers (adipokines, myokines, uremic toxins) were less predictive of 2-year cardiovascular mortality (15.5% in HD, 6.8% in PD) than age, nutrition, and inflammatory markers.
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