Periostin Predicts All-Cause Mortality in Male but Not Female End-Stage Renal Disease Patients on Hemodialysis
Language English Country Switzerland Media print-electronic
Document type Journal Article
PubMed
39004070
DOI
10.1159/000539765
PII: 000539765
Knihovny.cz E-resources
- Keywords
- All-cause mortality, Hemodialysis patients, Periostin, Sex dependency,
- MeSH
- Biomarkers blood MeSH
- Kidney Failure, Chronic * therapy mortality blood complications MeSH
- Renal Dialysis * MeSH
- Kaplan-Meier Estimate MeSH
- Middle Aged MeSH
- Humans MeSH
- Cell Adhesion Molecules * blood MeSH
- Periostin MeSH
- Cause of Death trends MeSH
- Prognosis MeSH
- Risk Factors MeSH
- ROC Curve MeSH
- Aged MeSH
- Sex Factors MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Biomarkers MeSH
- Cell Adhesion Molecules * MeSH
- Periostin MeSH
- POSTN protein, human MeSH Browser
INTRODUCTION: Periostin is a matricellular protein. Elevated serum concentrations of periostin have been reported in patients with various cardiovascular diseases, including heart failure. Patients with end-stage renal disease have a substantially increased risk for cardiovascular diseases. However, there is a lack of clinical studies to clarify the prognostic significance of systemic periostin on all-cause mortality in patients with end-stage renal disease on hemodialysis. METHODS: 313 stable end-stage renal disease patients were recruited and followed for 5 years concerning all-cause mortality. At baseline, we collected blood samples and clinical data. Serum periostin concentrations were measured using a certified ELISA. RESULTS: The optimal cut-off value for serum periostin regarding all-cause mortality, calculated through receiver operating characteristic analysis, was 777.5 pmol/L. Kaplan-Meier survival analysis using this cut-off value demonstrated that higher periostin concentrations are linked to higher all-cause mortality (log-rank test: p = 0.002). Subgroup analysis revealed that serum periostin concentrations only affected all-cause mortality in male but not in female patients (p = 0.002 in male patients and p = 0.474 in female patients). Multivariate Cox regression analyses, adjusted for confounding factors, likewise showed that elevated serum periostin concentrations were positively associated with all-cause mortality in male (p = 0.028) but not in female patients on hemodialysis (p = 0.313). CONCLUSION: Baseline serum periostin is an independent risk factor for all-cause mortality in male patients with chronic renal disease on hemodialysis.
2nd Medical Faculty Charles University of Prague Prague Czechia
Biomedica Slovakia s r o Bratislava Slovakia
Department of Medicine Charité Universitätsmedizin Berlin Berlin Germany
Department of Nephrology Odense University Hospital Odense Denmark
HMU Health and Medical University Potsdam Germany
Institute of Medical Diagnostics IMD Berlin Potsdam Berlin Germany
Reproductive and Genetic Hospital of CITIC Xiangya Changsha China
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