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DOI 10.1155/2017/7918472

Медицинская библиотека · Mediators of inflammation · 2017

The Correlation between FSTL1 Expression and Airway Remodeling in Asthmatics.

Liu Yahui, Liu Tian, Wu Jinxiang, Li Tao, Jiao Xingai, Zhang Haiqing, Zhao Jiping, Wang Junfei, Liu Lin, Cao Liuzhao, Li Shuo, Xu Jiawei, Xu Jianfeng, Ma Xiaohui, Yang Lei, Dong Liang

СтатьяПеревод пока не подготовлен

Аннотация

BACKGROUND

Asthma is characterized by airway remodeling. Follistatin-like protein 1 (FSTL1) is an extracellular glycoprotein. Recent studies suggest that FSTL1 may participate in the pathogenesis of asthma.

OBJECTIVES

To analyze the association between FSTL1 and some parameters and inspect the role of FSTL1 in asthma.

METHODS

We examined FSTL1 levels in 32 asthmatics and 25 controls. All subjects enrolled had routine blood tests, spirometry, and impulse oscillometry performed. Additionally, 15 of the 32 asthmatics underwent fibre optic bronchoscopy. Spearman rank analysis was performed to detect the correlation between FSTL1 and other parameters.

RESULTS

Plasma FSTL1 levels were higher in asthmatics (130.762 ± 46.029 ng/mL) than in controls (95.408 ± 33.938 ng/mL) (p = 0.009). Plasma FSTL1 levels were associated with fibrosis levels around the airways (rs = 0.529, p = 0.043) and α-smooth muscle actin (α-SMA) (rs = 0.554, p = 0.032). FSTL1 levels in bronchoalveolar lavage fluid were associated with collagen I (rs = 0.536, p = 0.040), α-SMA (rs = 0.561, p = 0.029), fibrosis levels (rs = 0.779, p = 0.001), and the thickness of the airway reticular basement membrane (RBM) (rs = 0.660, p = 0.007).

CONCLUSIONS

FSTL1 levels in asthmatics were linked with increased smooth muscle mass and thickened RBM. FSTL1 may contribute to airway remodeling in asthmatics.

Для цитирования: Liu Yahui, Liu Tian, Wu Jinxiang, Li Tao, Jiao Xingai, Zhang Haiqing, Zhao Jiping, Wang Junfei, Liu Lin, Cao Liuzhao, Li Shuo, Xu Jiawei, Xu Jianfeng, Ma Xiaohui, Yang Lei, Dong Liang. The Correlation between FSTL1 Expression and Airway Remodeling in Asthmatics.. Mediators of inflammation. 2017. DOI: 10.1155/2017/7918472.

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