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DOI 10.1177/0004563212473275

Медицинская библиотека · Annals of clinical biochemistry · 2013

Decreased levels of serum omentin-1 in patients with obstructive sleep apnoea syndrome.

Wang Qiuyan, Feng Xuewei, Zhou Chuming, Li Peng, Kang Jian

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Аннотация

BACKGROUND

Inflammation is involved in the mechanism of obstructive sleep apnoea syndrome (OSAS). Omentin, a newly discovered adipokine, is implicated to play an anti-inflammatory role. This study aims to determine whether serum levels of omentin-1 are associated with the presence and severity of OSAS.

METHODS

This study consisted of 192 patients with OSAS and 144 healthy subjects. Serum levels of omentin-1 were measured using enzyme-linked immunosorbent assay.

RESULTS

Serum omentin-1 levels were significantly decreased in OSAS patients compared with healthy controls. Multivariable logistic regression analysis revealed that serum omentin-1 levels were inversely associated with the presence of OSAS (odds ratio 0.520, 95% confidence interval 0.433 to 0.623; P < 0.001). Severe OSAS patients had significantly lower serum omentin-1 levels compared with mild and moderate OSAS patients. Spearman correlation analysis showed that serum omentin-1 levels were correlated with the severity of OSAS. Simple linear regression analysis showed that the serum levels of omentin-1 were negatively correlated with waist circumference, body mass index, systolic blood pressure, homeostasis model assessment of insulin resistance (HOMA-IR), C-reactive protein (CRP), and apnoea-hypopnoea index in patients with OSAS. Furthermore, only HOMA-IR and CRP remained inversely associated with serum omentin-1 after multiple stepwise regression analysis.

CONCLUSION

Decreased serum omentin-1 levels could be considered as an independent predictive marker of the presence and severity of OSAS.

Для цитирования: Wang Qiuyan, Feng Xuewei, Zhou Chuming, Li Peng, Kang Jian. Decreased levels of serum omentin-1 in patients with obstructive sleep apnoea syndrome.. Annals of clinical biochemistry. 2013. DOI: 10.1177/0004563212473275.

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