Circulating lipopolysaccharide-binding protein and carotid intima-media thickness in obstructive sleep apnea
Language English Country Czech Republic Media print-electronic
Document type Journal Article
PubMed
29137477
DOI
10.33549/physiolres.933632
PII: 933632
Knihovny.cz E-resources
- MeSH
- Biomarkers blood MeSH
- Adult MeSH
- Endotoxemia blood diagnosis physiopathology MeSH
- Carotid Intima-Media Thickness * trends MeSH
- Cohort Studies MeSH
- Middle Aged MeSH
- Humans MeSH
- Membrane Glycoproteins blood MeSH
- Sleep Apnea, Obstructive blood diagnosis physiopathology MeSH
- Polysomnography methods trends MeSH
- Acute-Phase Proteins MeSH
- Cross-Sectional Studies MeSH
- Risk Factors MeSH
- Carrier Proteins blood MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Biomarkers MeSH
- lipopolysaccharide-binding protein MeSH Browser
- Membrane Glycoproteins MeSH
- Acute-Phase Proteins MeSH
- Carrier Proteins MeSH
Circulating lipopolysaccharide-binding protein (LBP), a metabolic endotoxemia marker, was identified as an independent predictor of atherosclerosis. Although increases in carotid intima-media thickness (CIMT) were repeatedly reported in obstructive sleep apnea (OSA), neither the role of OSA in metabolic endotoxemia nor of LBP in early atherosclerosis were explored in patients with OSA. At a tertiary university hospital we investigated the relationships between OSA, LBP and CIMT in 117 men who underwent full polysomnography and CIMT assessment by B-mode ultrasound. Circulating LBP concentrations and average CIMT increased from patients without OSA to those with mild-moderate and severe OSA (from 32.1+/-10.3 to 32.3+/-10.9 to 38.1+/-10.3 microg.ml(-1), p=0.015; from 0.52+/-0.09 to 0.58+/-0.06 to 0.62+/-0.10 mm, p=0.004, respectively). Oxygen desaturation index (ODI) was a predictor of serum LBP levels independent of age, waist-to-hip ratio (WHR), smoking, hypertension, HDL cholesterol, triglycerides and fasting glucose [p (ANOVA)=0.002, r(2)=0.154], with no independent effect of the ODI*WHR interaction term on LBP. Furthermore, serum LBP predicted CIMT independently of known risk factors of atherosclerosis including obesity (p<0.001, r(2)=0.321). Our results suggest that OSA severity contributes to metabolic endotoxemia in patients with OSA independently of obesity, and that LBP might represent a contributing factor promoting early atherosclerosis in such patients.
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