Wang Xiao-ru, Li Yong-pu, Gao Shui, Xia Wei, Gao Kun, Kong Qing-hua, Qi Hui, Wu Ling, Zhang Jing, Qu Jie-ming, Bai Chun-xue
Department of Pulmonary Medicine, Dahua Hospital, Xuhui District, Shanghai, People's Republic of China.
Department of Pulmonary Medicine, People's Hospital of Changshou, Chongqing, Shanghai, People's Republic of China.
Int J Chron Obstruct Pulmon Dis. 2014 May 27;9:543-9. doi: 10.2147/COPD.S62700. eCollection 2014.
Despite a number of studies on biomarkers in chronic obstructive pulmonary disease (COPD), only a few disease-related markers have been identified, yet we still have no satisfactory markers specific to innate immune system and neutrophil activation, which is essential in airway inflammation in COPD. Recent biological studies indicated that lipocalins (LCNs) might be involved in airway inflammation and innate immunity; however, results from available studies on the association of LCNs with COPD are not consistent. We carried out a multicenter prospective observational cohort study to investigate the differences in serum levels of LCN1 and LCN2 between subjects with COPD (n=58) and healthy controls (n=29). Several validated inflammatory markers, including C-reactive protein, tumor necrosis factor-α, interleukin-6, and interleukin-8, were measured. The correlation of LCN1 and LCN2 with clinical features such as smoking habits, lung function, symptoms, and disease category was also analyzed. When comparing with healthy controls, serum levels of LCN1 (66.35±20.26 ng/mL versus 41.16±24.19 ng/mL, P<0.001) and LCN2 (11.29±3.92 ng/mL versus 6.09±5.13 ng/mL, P<0.001) were both elevated in subjects with COPD after adjusting for age, sex, smoking habits, and inflammatory biomarkers. Smoking history and tobacco exposure, as quantified by pack-year, had no impact on systemic expressions of LCN1 and LCN2 in our study. Blood levels of LCN1 and LCN2, respectively, were negatively correlated to COPD Assessment Test and Modified Medical British Research Council score (P<0.001). Disease category by Global Initiative for Chronic Obstructive Lung Disease grade 1-4 or group A-D was not associated with levels of LCNs. Patient-reported exacerbations and body mass index were also tested, but no relationship with LCNs was found. In summary, serum concentrations of LCN1 and LCN2 were both elevated in patients with COPD, with their levels correlating to COPD Assessment Test and Modified Medical British Research Council score. These findings warrant large-scale and longitudinal studies to validate LCNs as circulating biomarkers for COPD.
尽管针对慢性阻塞性肺疾病(COPD)的生物标志物开展了多项研究,但仅识别出少数与疾病相关的标志物,而且我们仍未找到针对先天性免疫系统和中性粒细胞活化的令人满意的特异性标志物,而这在COPD的气道炎症中至关重要。近期的生物学研究表明,脂质运载蛋白(LCNs)可能参与气道炎症和先天性免疫;然而,关于LCNs与COPD关联的现有研究结果并不一致。我们开展了一项多中心前瞻性观察性队列研究,以调查慢性阻塞性肺疾病患者(n = 58)和健康对照者(n = 29)血清中LCN1和LCN2水平的差异。检测了几种经过验证的炎症标志物,包括C反应蛋白、肿瘤坏死因子-α、白细胞介素-6和白细胞介素-8。还分析了LCN1和LCN2与吸烟习惯、肺功能、症状和疾病类别等临床特征的相关性。与健康对照者相比,在调整年龄、性别、吸烟习惯和炎症生物标志物后,COPD患者的血清LCN1水平(66.35±20.26 ng/mL对41.16±24.19 ng/mL,P<0.001)和LCN2水平(11.29±3.92 ng/mL对6.09±5.13 ng/mL,P<0.001)均升高。在我们的研究中,吸烟史和以包年量化的烟草暴露对LCN1和LCN2的全身表达没有影响。LCN1和LCN2的血液水平分别与COPD评估测试和改良英国医学研究委员会评分呈负相关(P<0.001)。慢性阻塞性肺疾病全球倡议1 - 4级或A - D组的疾病类别与LCNs水平无关。还对患者报告的病情加重情况和体重指数进行了检测,但未发现与LCNs有关联。总之,COPD患者血清中LCN1和LCN2的浓度均升高,其水平与COPD评估测试和改良英国医学研究委员会评分相关。这些发现需要大规模的纵向研究来验证LCNs作为COPD循环生物标志物的作用。