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慢性阻塞性肺疾病(COPD)患者血清IgE升高和曲霉菌致敏的患病率及其与症状和肺功能的关系。

The prevalence of increased serum IgE and Aspergillus sensitization in patients with COPD and their association with symptoms and lung function.

作者信息

Jin Jianmin, Liu Xiaofang, Sun Yongchang

机构信息

Department of Respiratory Medicine, Beijing Tongren Hospital, Capital Medical University, Beijing, China.

出版信息

Respir Res. 2014 Oct 29;15(1):130. doi: 10.1186/s12931-014-0130-1.

DOI:10.1186/s12931-014-0130-1
PMID:25359094
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4216660/
Abstract

BACKGROUND

Allergy and Aspergillus hypersensitivity (AH) were shown to be associated with severe symptoms or worse lung function in COPD patients. The prevalence of elevated total IgE (T-IgE) and its association with clinical symptoms and lung function in COPD have not been studied. The prevalence of AH and its correlation with clinical characteristics in a COPD cohort of larger sample size is also lacking.

METHODS

273 patients with COPD were evaluated by respiratory symptoms, blood test, chest HRCT, lung function, serum detection of T-IgE and Aspergillus specific IgE. Patients with T-IgE ≥ 1000 KU/L were further investigated for allergic bronchopulmonary aspergillosis (ABPA).

RESULTS

The prevalence of elevated T-IgE and AH in patients with COPD was 47.3% and 15.0%, respectively. Eight patients (2.9%) met the diagnostic criteria for ABPA. Compared with the normal T-IgE group, patients with elevated T-IgE had a longer history of dyspnea (p < 0.01), an earlier onset of dyspnea after chronic cough/expectoration (p < 0.01), and were more likely to wheeze (p < 0.01). They also showed worse lung functions and more severe GOLD staging (p < 0.01). Analysis of the clinical data in male patients with smoking as the risk factor showed the same results. To evaluate the clinical characteristics of COPD with AH, patients with elevated T-IgE were further divided into subgroups with and without AH. When compared with the normal T-IgE group, both the two subgroups showed longer history of dyspnea (p < 0.01), an earlier onset of dyspnea (p < 0.01) and a worse status of lung function (p < 0.05). Correlation analysis demonstrated that T-IgE was correlated positively with the time length of dyspnea (r = 0.401, p < 0.001), and the ratio of duration of dyspnea to that of chronic cough/expectoration (r = 0.59, p < 0.001), but negatively with FEV1/FVC% (r = -0.194, p = 0.001), and FEV1%predicted (r = -0.219, p < 0.001).

CONCLUSIONS

There was a high prevalence of elevated serum T-IgE and AH in patients with COPD. Serum T-IgE level was correlated with symptoms such as dyspnea and impairment of lung function. Allergens other than Aspergillus may have similar effects on disease expression or progression of COPD.

摘要

背景

过敏和曲霉菌超敏反应(AH)与慢性阻塞性肺疾病(COPD)患者的严重症状或更差的肺功能相关。COPD患者中总IgE(T-IgE)升高的患病率及其与临床症状和肺功能的关系尚未得到研究。大样本量的COPD队列中AH的患病率及其与临床特征的相关性也尚不明确。

方法

对273例COPD患者进行呼吸症状、血液检查、胸部高分辨率CT、肺功能、血清T-IgE及曲霉菌特异性IgE检测。对T-IgE≥1000 KU/L的患者进一步检查是否患有变应性支气管肺曲霉菌病(ABPA)。

结果

COPD患者中T-IgE升高和AH的患病率分别为47.3%和15.0%。8例患者(2.9%)符合ABPA诊断标准。与T-IgE正常组相比,T-IgE升高的患者呼吸困难病史更长(p<0.01),慢性咳嗽/咳痰后出现呼吸困难的时间更早(p<0.01),且更易出现喘息(p<0.01)。他们的肺功能也更差,GOLD分期更严重(p<0.01)。以吸烟为危险因素的男性患者临床数据分析显示结果相同。为评估合并AH的COPD的临床特征,将T-IgE升高的患者进一步分为合并AH和未合并AH的亚组。与T-IgE正常组相比,两个亚组的呼吸困难病史均更长(p<0.01),呼吸困难出现更早(p<0.01),肺功能状况更差(p<0.05)。相关性分析表明,T-IgE与呼吸困难时长(r=0.401,p<0.001)、呼吸困难持续时间与慢性咳嗽/咳痰持续时间的比值(r=0.59,p<0.001)呈正相关,但与FEV1/FVC%(r=-0.194,p=0.001)和预计FEV1%(r=-0.219,p<0.001)呈负相关。

结论

COPD患者血清T-IgE升高和AH的患病率较高。血清T-IgE水平与呼吸困难等症状及肺功能损害相关。除曲霉菌外的过敏原可能对COPD的疾病表现或进展有类似影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a90/4216660/9a4c0d8d02a1/12931_2014_130_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a90/4216660/9b615498ea63/12931_2014_130_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a90/4216660/34adea2635cc/12931_2014_130_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a90/4216660/1020405b8ac5/12931_2014_130_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a90/4216660/9a4c0d8d02a1/12931_2014_130_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a90/4216660/9b615498ea63/12931_2014_130_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a90/4216660/34adea2635cc/12931_2014_130_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a90/4216660/1020405b8ac5/12931_2014_130_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2a90/4216660/9a4c0d8d02a1/12931_2014_130_Fig4_HTML.jpg

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