Serum S100A12 (EN-RAGE) levels in patients with decreased renal function and subclinical chronic inflammatory disease
Jazyk angličtina Země Švýcarsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21822023
DOI
10.1159/000329291
PII: 000329291
Knihovny.cz E-zdroje
- MeSH
- biologické markery krev MeSH
- chronická renální insuficience krev patologie patofyziologie MeSH
- chronické selhání ledvin krev patologie patofyziologie MeSH
- dospělí MeSH
- ledviny metabolismus patofyziologie MeSH
- lidé středního věku MeSH
- lidé MeSH
- mediátory zánětu krev MeSH
- protein S100A12 MeSH
- proteiny S100 krev MeSH
- senioři MeSH
- vyšetření funkce ledvin metody MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- biologické markery MeSH
- mediátory zánětu MeSH
- protein S100A12 MeSH
- proteiny S100 MeSH
- S100A12 protein, human MeSH Prohlížeč
BACKGROUND: The calcium-binding protein S100A12 (EN-RAGE) causes inflammation through interaction with the multiligand receptor for advanced glycation end products (RAGE). The aim of the study was to determine S100A12 levels and describe their relationship to inflammatory markers in patients with decreased renal function. METHODS: The studied group consisted of 46 patients with various degrees of chronic renal insufficiency (CHRI), 31 long-term hemodialysis (HD) patients and 24 healthy controls. S100A12 and soluble RAGE were assessed immunochemically (ELISA), and routine biochemical parameters were measured. RESULTS: S100A12 levels were not different in CHRI (166 ± 140 ng/ml) and HD patients (127 ± 101 ng/ml) compared to controls (126 ± 106 ng/ml; p = 0.20, n.s.). In CHRI patients, S100A12 correlated with C-reactive protein (CRP) levels, orosomucoid, and inversely with α(2)-macroglobulin. In HD patients, S100A12 correlated with age, CRP, orosomucoid, fibrinogen and leukocyte levels. In multivariate regression analysis after adjustment for age, S100A12 levels remained correlated with: orosomucoid in CHRI patients; CRP, leukocytes, fibrinogen and negatively with sRAGE in HD patients; and leukocytes in controls. CONCLUSIONS: Although S100A12 levels were not elevated in patients with decreased kidney function, a relation to markers of inflammation was found. Further studies are required to demonstrate the significance of S100A12 in patients with decreased renal function.
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