免疫球蛋白E作为特应性哮喘和慢性阻塞性肺疾病重叠的生物标志物

C. Hersh, Soumya Zacharia, Ram Prakash Arivu Chelvan, L. Hayden, A. Mirtar, S. Zarei, N. Putcha
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引用次数: 19

摘要

哮喘-慢性阻塞性肺病重叠(ACO)是一种常见的临床综合征,但没有单一客观的定义。我们假设免疫球蛋白E (IgE)测量可用于细化ACO的定义。在COPD遗传流行病学(COPDGene®)研究的2870名参与者的基线血浆样本中,我们测量了6种常见过敏原的总IgE水平和特异性IgE水平。与通常的慢性阻塞性肺疾病(COPD)相比,ACO参与者(基于哮喘自我报告)的总IgE水平更高(中位数为67.0对42.2 IU/ml),并且更频繁地至少有一种特异性IgE阳性(43.5%对24.5%)。我们之前在COPD患者中使用了严格的ACO定义,基于40岁前医生诊断哮喘的自我报告。这种严格的ACO定义因特应性的存在而得到完善,由总IgE bb0 100 IU/ml或至少一种阳性特异性IgE确定,正如基于自我报告的哮喘史的ACO的更广泛定义一样。所有3种ACO定义的参与者都更年轻(平均年龄60.0-61.3岁),更常见的是非裔美国人(36.8%-44.2%),有更高的加重频率(过去一年1.0-1.2),胸部计算机断层扫描(CT)定量分析显示气道壁增厚更多。在ACO患者中,37%-46%的人没有特应性反应;这些人在胸部CT扫描中有更多的肺气肿。基于与急性加重和CT气道疾病的关联,IgE并没有明显改善ACO的临床定义。然而,IgE测量可用于细分特应性和非特应性ACO个体,他们可能具有不同的生物学机制和潜在的治疗方法。
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Immunoglobulin E as a Biomarker for the Overlap of Atopic Asthma and Chronic Obstructive Pulmonary Disease.
Asthma-COPD overlap (ACO) is a common clinical syndrome, yet there is no single objective definition. We hypothesized that immunoglobulin E (IgE) measurements could be used to refine the definition of ACO. In baseline plasma samples from 2870 participants in the COPD Genetic Epidemiology (COPDGene®) study, we measured total IgE levels and specific IgE levels to 6 common allergens. Compared to usual chronic obstructive pulmonary disease (COPD), participants with ACO (based on self-report of asthma) had higher total IgE levels (median 67.0 versus 42.2 IU/ml) and more frequently had at least one positive specific IgE (43.5% versus 24.5%). We previously used a strict definition of ACO in participants with COPD, based on self-report of a doctor's diagnosis of asthma before age 40. This strict ACO definition was refined by the presence of atopy, determined by total IgE > 100 IU/ml or at least one positive specific IgE, as was the broader definition of ACO based on self-reported asthma history. Participants with all 3 ACO definitions were younger (mean age 60.0-61.3 years), were more commonly African American (36.8%-44.2%), had a higher exacerbation frequency (1.0-1.2 in the past year), and had more airway wall thickening on quantitative analysis of chest computed tomography (CT) scans. Among participants with ACO, 37%-46% did not have atopy; these individuals had more emphysema on chest CT scan. Based on associations with exacerbations and CT airway disease, IgE did not clearly improve the clinical definition of ACO. However, IgE measurements could be used to subdivide individuals with atopic and non-atopic ACO, who might have different biologic mechanisms and potential treatments.
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