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Circulating levels of clusterin and complement factor H in patients with obstructive sleep apnea
Martina Meszaros1, Peter Horvath1, Adrian Kis1
1Department of Pulmonology, Semmelweis University, Budapest, Hungary.
Insights
Obstructive sleep apnea (OSA) activates the complement system. Researchers found higher clusterin levels in OSA patients, suggesting it may protect against membrane attack complex (MAC) formation.
Area of Science:
- Immunology
- Sleep Medicine
- Biochemistry
Background:
- Obstructive sleep apnea (OSA) is linked to complement system activation.
- Despite activation, membrane attack complex (MAC) levels remain unchanged in OSA, indicating regulatory mechanisms.
- Complement factor H (CFH) and clusterin are key regulators of the complement system.
Purpose of the Study:
- To investigate the levels of complement regulators CFH and clusterin in patients with OSA.
- To explore the potential role of these regulators in the pathophysiology of OSA.
Main Methods:
- Plasma samples from 86 OSA patients and 33 control subjects were analyzed.
- Quantification of clusterin and CFH levels was performed using plasma assays.
Main Results:
- No significant difference in CFH levels was observed between OSA patients and controls.
- Clusterin levels were significantly higher in OSA patients compared to controls.
- A trend towards a positive correlation between clusterin levels and OSA severity was noted.
Conclusions:
- Elevated clusterin levels in OSA patients may play a protective role.
- Increased clusterin might inhibit MAC formation, potentially mitigating complement-mediated damage in OSA.
- Further research is warranted to elucidate the precise role of clusterin in OSA.
Abstract:
Aim: Obstructive sleep apnea (OSA) activates the complement system; however, the levels of membrane attack complex (MAC) are unaltered suggesting regulatory mechanisms. Our aim was to investigate complement factor H (CFH) and clusterin, two important complement regulators in OSA. Materials & methods: We analyzed clusterin and CFH levels in plasma of 86 patients with OSA and 33 control subjects. Results: There was no difference in CFH levels between patients (1099.4/784.6-1570.5/μg/ml) and controls (1051.4/652.0-1615.1/μg/ml, p = 0.72). Clusterin levels were higher in patients with OSA (309.7/217.2-763.2/μg/ml vs 276.1/131.0-424.3/μg/ml, p = 0.048) with a trend for a positive correlation with disease severity (p = 0.073). Conclusion: Increase in clusterin levels may be protective in OSA by blocking the MAC formation.
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