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循环中纤溶酶原激活物抑制剂-1(PAI-1)水平升高与慢性阻塞性肺疾病患者的肺功能下降、全身炎症及小气道阻塞有关。

Elevated circulating PAI-1 levels are related to lung function decline, systemic inflammation, and small airway obstruction in chronic obstructive pulmonary disease.

作者信息

Wang Hao, Yang Ting, Li Diandian, Wu Yanqiu, Zhang Xue, Pang Caishuang, Zhang Junlong, Ying Binwu, Wang Tao, Wen Fuqiang

机构信息

Department of Respiratory and Critical Care Medicine, West China Hospital of Sichuan University, Chengdu, Sichuan, People's Republic of China; Division of Pulmonary Diseases, State Key Laboratory of Biotherapy of China, West China Hospital of Sichuan University, Chengdu, Sichuan, People's Republic of China.

Department of Laboratory Medicine, West China Hospital of Sichuan University, Chengdu, Sichuan, People's Republic of China.

出版信息

Int J Chron Obstruct Pulmon Dis. 2016 Sep 26;11:2369-2376. doi: 10.2147/COPD.S107409. eCollection 2016.

Abstract

BACKGROUND

Plasminogen activator inhibitor-1 (PAI-1) and soluble urokinase-type plasminogen activator receptor (suPAR) participate in inflammation and tissue remolding in various diseases, but their roles in chronic obstructive pulmonary disease (COPD) are not yet clear. This study aimed to investigate if PAI-1 and suPAR were involved in systemic inflammation and small airway obstruction (SAO) in COPD.

METHODS

Demographic and clinical characteristics, spirometry examination, and blood samples were obtained from 84 COPD patients and 51 healthy volunteers. Serum concentrations of PAI-1, suPAR, tissue inhibitor of metalloproteinase-1 (TIMP-1), Matrix metalloproteinase-9 (MMP-9), and C-reactive protein (CRP) were detected with Magnetic Luminex Screening Assay. Differences between groups were statistically analyzed using one-way analysis of variance or chi-square test. Pearson's partial correlation test (adjusted for age, sex, body mass index, cigarette status, and passive smoke exposure) and multivariable linear analysis were used to explore the relationships between circulating PAI-1 and indicators of COPD.

RESULTS

First, we found that serum PAI-1 levels but not suPAR levels were significantly increased in COPD patients compared with healthy volunteers (125.56±51.74 ng/mL versus 102.98±36.62 ng/mL, =0.007). Then, the correlation analysis showed that circulating PAI-1 was inversely correlated with pulmonary function parameters including the ratio of forced expiratory volume in 1 second to forced vital capacity (FEV/FVC), FEV/Pre (justified =-0.308, <0.001; justified =-0.295, =0.001, respectively) and SAO indicators such as FEV/FVC, MMEF25-75/Pre (justified =-0.289, =0.001; justified =-0.273, =0.002, respectively), but positively related to the inflammatory marker CRP (justified =0.351, <0.001), the small airway remolding biomarker TIMP-1, and MMP-9 (justified =0.498, <0.001; justified =0.267, =0.002, respectively). Besides, multivariable linear analysis showed that FEV/FVC, CRP, and TIMP-1 were independent parameters associated with PAI-1.

CONCLUSION

Our findings first illustrate that elevated serum PAI-1 levels are related to the lung function decline, systemic inflammation, and SAO in COPD, suggesting that PAI-1 may play critical roles in the pathogenesis of COPD.

摘要

背景

纤溶酶原激活物抑制剂-1(PAI-1)和可溶性尿激酶型纤溶酶原激活物受体(suPAR)参与多种疾病的炎症反应和组织重塑,但其在慢性阻塞性肺疾病(COPD)中的作用尚不清楚。本研究旨在探讨PAI-1和suPAR是否参与COPD的全身炎症反应和小气道阻塞(SAO)。

方法

收集84例COPD患者和51例健康志愿者的人口统计学和临床特征、肺功能检查结果及血样。采用磁珠免疫分析检测血清中PAI-1、suPAR、基质金属蛋白酶组织抑制剂-1(TIMP-1)、基质金属蛋白酶-9(MMP-9)和C反应蛋白(CRP)的浓度。采用单因素方差分析或卡方检验对组间差异进行统计学分析。采用Pearson偏相关检验(校正年龄、性别、体重指数、吸烟状况和被动吸烟暴露)和多变量线性分析探讨循环PAI-1与COPD指标之间的关系。

结果

首先,我们发现与健康志愿者相比,COPD患者血清PAI-1水平显著升高,但suPAR水平无显著变化(125.56±51.74 ng/mL对102.98±36.62 ng/mL,P=0.007)。然后,相关性分析显示,循环PAI-1与肺功能参数呈负相关,包括第1秒用力呼气容积与用力肺活量之比(FEV1/FVC)、FEV1/预计值(校正r=-0.308,P<0.001;校正r=-0.295,P=0.001),以及SAO指标如FEV1/FVC、MMEF25-75/预计值(校正r=-0.289,P=0.001;校正r=-0.273,P=0.002),但与炎症标志物CRP(校正r=0.351,P<0.001)、小气道重塑生物标志物TIMP-1和MMP-9呈正相关(校正r=0.498,P<0.001;校正r=0.267,P=0.002)。此外,多变量线性分析显示,FEV1/FVC、CRP和TIMP-1是与PAI-1相关的独立参数。

结论

我们的研究结果首次表明,血清PAI-1水平升高与COPD患者的肺功能下降、全身炎症反应和SAO有关,提示PAI-1可能在COPD的发病机制中起关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6271/5044991/1d78f9e34218/copd-11-2369Fig1.jpg

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