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Decreased levels of serum nesfatin-1 in patients with obstructive sleep apnea syndrome

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Abstract

Purpose

Recent evidences suggest that inflammation is involved in the mechanism of obstructive sleep apnea syndrome (OSAS). Nesfatin-1, recently identified as the satiety regulator, is implicated to possess an anti-inflammatory effect. The aim of our study is to investigate whether serum levels of nesfatin-1 are associated with the presence and severity of OSAS.

Methods

A total of 196 patients with OSAS and 104 healthy subjects were enrolled in this study. Serum levels of nesfatin-1 were measured by enzyme-linked immunosorbent assay.

Results

OSAS patients showed significantly reduced levels of serum nesfatin-1 levels than healthy controls. Multivariable logistic regression analysis indicates that serum nesfatin-1 levels were inversely associated with the presence of OSAS (odds ration (OR) 0.003, 95 % confidence interval (CI) 0.001 to 0.017; P < 0.001). Serum levels of nesfatin-1 were significantly decreased in severe OSAS patients compared with mild and moderate OSAS patients. Spearman correlation analysis showed that serum nesfatin-1 levels were inversely correlated with the severity of OSAS. In addition, Spearman correlation analysis showed that serum nesfatin-1 levels were negatively correlated with body mass index (BMI) (r = −0.299, P < 0.001), waist–hip ratio (WHR) (r = −0.277, P < 0.001), homeostasis model assessment of insulin resistance (HOMA-IR) (r = −0.338, P < 0.001), and apnea–hypopnea index (AHI) (r = −0.248, P < 0.001) in patients with OSAS.

Conclusions

Decreased serum nesfatin-1 levels are associated with the presence and severity of OSAS.

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Science Funding of Tianjin First Center Hospital (SFTFCH120)

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Correspondence to Yu Wang.

Additional information

Peng Shen and Yingying Han contributed equally to this article

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Shen, P., Han, Y., Cai, B. et al. Decreased levels of serum nesfatin-1 in patients with obstructive sleep apnea syndrome. Sleep Breath 19, 515–522 (2015). https://doi.org/10.1007/s11325-014-1039-0

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  • DOI: https://doi.org/10.1007/s11325-014-1039-0

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