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基于临床特征的数据分析驱动的成人哮喘表型与二十年后的哮喘结局相关。

Data-driven adult asthma phenotypes based on clinical characteristics are associated with asthma outcomes twenty years later.

机构信息

IAB, Team of Environmental Epidemiology Applied To Reproduction and Respiratory Health, INSERM, Université Grenoble Alpes, CNRS, Grenoble, France.

Faculté de Pharmacie, Université Grenoble Alpes, Grenoble, France.

出版信息

Allergy. 2019 May;74(5):953-963. doi: 10.1111/all.13697. Epub 2019 Jan 15.

Abstract

BACKGROUND

Research based on cluster analyses led to the identification of particular phenotypes confirming phenotypic heterogeneity of asthma. The long-term clinical course of asthma phenotypes defined by clustering analysis remains unknown, although it is a key aspect to underpin their clinical relevance. We aimed to estimate risk of poor asthma events between asthma clusters identified 20 years earlier.

METHODS

The study relied on two cohorts of adults with asthma with 20-year follow-up, ECRHS (European Community Respiratory Health Survey) and EGEA (Epidemiological study on Genetics and Environment of Asthma). Regression models were used to compare asthma characteristics (current asthma, asthma exacerbations, asthma control, quality of life, and FEV ) at follow-up and the course of FEV  between seven cluster-based asthma phenotypes identified 20 years earlier.

RESULTS

The analysis included 1325 adults with ever asthma. For each asthma characteristic assessed at follow-up, the risk for adverse outcomes differed significantly between the seven asthma clusters identified at baseline. As compared with the mildest asthma phenotype, ORs (95% CI) for asthma exacerbations varied from 0.9 (0.4 to 2.0) to 4.0 (2.0 to 7.8) and the regression estimates (95% CI) for FEV % predicted varied from 0.6 (-3.5 to 4.6) to -9.9 (-14.2 to -5.5) between clusters. Change in FEV over time did not differ significantly across clusters.

CONCLUSION

Our findings show that the long-term risk for poor asthma outcomes differed between comprehensive adult asthma phenotypes identified 20 years earlier, and suggest a strong tracking of asthma activity and impaired lung function over time.

摘要

背景

基于聚类分析的研究导致了特定表型的识别,这些表型证实了哮喘表型异质性。通过聚类分析定义的哮喘表型的长期临床病程尚不清楚,尽管这是支持其临床相关性的关键方面。我们旨在估计 20 年前确定的哮喘聚类之间不良哮喘事件的风险。

方法

该研究依赖于两个具有 20 年随访的成年人哮喘队列,ECRHS(欧洲社区呼吸健康调查)和 EGEA(哮喘遗传学和环境的流行病学研究)。回归模型用于比较随访时的哮喘特征(当前哮喘、哮喘加重、哮喘控制、生活质量和 FEV )和 20 年前确定的基于聚类的七个哮喘表型之间的 FEV 进程。

结果

该分析包括 1325 名有过哮喘的成年人。对于在随访时评估的每种哮喘特征,在基线时确定的七个哮喘聚类之间,不良结局的风险差异显著。与最轻微的哮喘表型相比,哮喘加重的 OR(95%CI)从 0.9(0.4 至 2.0)到 4.0(2.0 至 7.8)不等,而 FEV %预测的回归估计(95%CI)从 0.6(-3.5 至 4.6)到-9.9(-14.2 至-5.5)不等。不同聚类之间的 FEV 随时间的变化没有显著差异。

结论

我们的研究结果表明,20 年前确定的综合成人哮喘表型之间的长期不良哮喘结局风险不同,并表明随着时间的推移,哮喘活动和肺功能受损具有很强的追踪性。

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