EN-RAGE (extracellular newly identified receptor for advanced glycation end-products binding protein) and mortality of long-term hemodialysis patients: A prospective observational cohort study
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
22394461
DOI
10.1016/j.clinbiochem.2012.02.014
PII: S0009-9120(12)00091-4
Knihovny.cz E-resources
- MeSH
- Biomarkers blood MeSH
- C-Reactive Protein analysis MeSH
- Time Factors MeSH
- Renal Dialysis mortality MeSH
- Infections metabolism mortality MeSH
- Cardiovascular Diseases metabolism mortality MeSH
- Cohort Studies MeSH
- Middle Aged MeSH
- Humans MeSH
- Multivariate Analysis MeSH
- Prognosis MeSH
- Proportional Hazards Models MeSH
- Prospective Studies MeSH
- S100A12 Protein MeSH
- S100 Proteins blood MeSH
- Aged MeSH
- Case-Control Studies MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Aged MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Biomarkers MeSH
- C-Reactive Protein MeSH
- S100A12 Protein MeSH
- S100 Proteins MeSH
- S100A12 protein, human MeSH Browser
OBJECTIVES: EN-RAGE is extracellular newly identified receptor for advanced glycation end-products binding protein playing a role in inflammation. The aim was to test the relationship of EN-RAGE to prognosis of long-term hemodialysis patients (HD). DESIGN AND METHODS: This is a prospective observational cohort study in 261 HD patients followed up for five years. Laboratory parameters were measured at the beginning of the study. RESULTS: EN-RAGE was slightly but unsignificantly increased in HD patients compared with healthy controls and correlated significantly with inflammatory markers. Univariate Cox analysis demonstrated EN-RAGE as a significant predictor for mortality due to infection (HR (95%CI): 1.305 (1.063-1.602), per standard deviation, p=0.01), but this significance disappeared in multivariate Cox analysis when CRP was included into the model. CONCLUSIONS: Our study demonstrates EN-RAGE as an inflammatory biomarker. It is related to mortality of HD patients due to infection, but in our study, it did not provide additional information to CRP.
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