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Biological clustering supports both 'Dutch'' and 'British'' hypotheses of asthma and chronic obstructive pulmonary disease

机译:生物聚类支持哮喘和慢性阻塞性肺疾病的“荷兰”和“英国”假设

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Background: Asthma and chronic obstructive pulmonary disease (COPD) are heterogeneous diseases. Objective: We sought to determine, in terms of their sputum cellular and mediator profiles, the extent to which they represent distinct or overlapping conditions supporting either the "British'' or "Dutch'' hypotheses of airway disease pathogenesis. Methods: We compared the clinical and physiological characteristics and sputum mediators between 86 subjects with severe asthma and 75 with moderate-to-severe COPD. Biological subgroups were determined using factor and cluster analyses on 18 sputum cytokines. The subgroups were validated on independent severe asthma (n = 166) and COPD (n = 58) cohorts. Two techniques were used to assign the validation subjects to subgroups: linear discriminant analysis, or the best identified discriminator (single cytokine) in combination with subject disease status (asthma or COPD). Results: Discriminant analysis distinguished severe asthma from COPD completely using a combination of clinical and biological variables. Factor and cluster analyses of the sputum cytokine profiles revealed 3 biological clusters: cluster 1: asthma predominant, eosinophilic, high T(H)2 cytokines; cluster 2: asthma and COPD overlap, neutrophilic; cluster 3: COPD predominant, mixed eosinophilic and neutrophilic. Validation subjects were classified into 3 subgroups using discriminant analysis, or disease status with a binary assessment of sputum IL-1 beta expression. Sputum cellular and cytokine profiles of the validation subgroups were similar to the subgroups from the test study. Conclusions: Sputum cytokine profiling can determine distinct and overlapping groups of subjects with asthma and COPD, supporting both the British and Dutch hypotheses. These findings may contribute to improved patient classification to enable stratified medicine.
机译:背景:哮喘和慢性阻塞性肺疾病(COPD)是异质性疾病。目的:我们试图根据痰的细胞和介导物特征,确定它们代表气道疾病发病机理的“英国”或“荷兰”假设的不同或重叠条件的程度。方法:我们比较了86例重度哮喘患者和75例中度至重度COPD患者的临床和生理特征以及痰液介质。使用因子和聚类分析对18种痰液细胞因子确定生物学亚组。亚组在独立的严重哮喘(n = 166)和COPD(n = 58)队列中得到验证。使用两种技术将验证对象分配给亚组:线性判别分析,或与对象疾病状况(哮喘或COPD)相结合的最佳识别判别器(单细胞因子)。结果:判别分析结合临床和生物学变量,将重度哮喘与COPD完全区分开。痰细胞因子谱的因子和聚类分析揭示了3个生物簇:簇1:哮喘为主,嗜酸性,高T(H)2细胞因子;第2类:哮喘和COPD重叠,嗜中性;第三类:COPD为主,嗜酸性和嗜中性混合。使用判别分析或疾病状态通过对痰液IL-1β表达进行二元评估,将验证对象分为3个亚组。验证亚组的痰细胞和细胞因子谱与测试研究中的亚组相似。结论:痰细胞因子谱分析可以确定哮喘和COPD受试者的不同和重叠的组,支持英国和荷兰的假设。这些发现可能有助于改善患者分类,从而使药物分层。

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