2型炎症及性别对哮喘加重率的影响

Trisha Agarwal BS , Ryan Peterson PhD , Guillermo Jimenez MD , Zachary Taich MD , Sunita Sharma MD, MPH , Fernando Holguin MD, MPH , Meghan D. Althoff MD, PhD
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引用次数: 0

摘要

先前的研究已经确定了哮喘恶化的预测因素;然而,大多数缺乏2型(T2)炎症标志物的整合。研究问题:在一个大型电子健康记录数据库中,哮喘加重率的预测因子是什么? T2炎症、女性性别和肥胖是否存在相互作用?研究设计和方法这是一项回顾性队列研究,使用在uhealth系统中随访至少1年的哮喘患者的电子健康记录数据。主要结局是哮喘加重率,由口服皮质类固醇的处方定义。感兴趣的预测因素包括T2高炎症,定义为绝对嗜酸性粒细胞计数(AEC)≥300细胞/μL, BMI和性别。加重次数和预先指定的相互作用的预测因子用负二项模型确定。采用自然三次样条曲线模拟AEC与急性加重率之间的剂量响应。结果纳入70939例哮喘患者;52%的患者患有T2高炎症,62%的患者为女性,70%的患者超重或肥胖。T2高炎症个体的调整加重率更高(调整发病率比,1.13;95% CI, 1.10-1.16)。AEC预测急性发作频率呈剂量依赖性。性别差异显著,T2高炎症的女性受试者与T2高炎症的男性受试者相比,加重率增加。本研究发现T2高炎症伴哮喘患者的加重率增加,并表现出对AEC的剂量依赖性反应。据我们所知,这是第一个发现性别和T2状态影响的研究,确定了一组可能从T2靶向生物治疗中获益的患者,以降低他们的恶化率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of Effect Modification of Type 2 Inflammation and Sex on Asthma Exacerbation Rates

Background

Prior studies have identified predictors of asthma exacerbations; however, most lack integration of type 2 (T2) inflammatory markers.

Research Question

In a large electronic health record database, what are predictors of asthma exacerbation rates and is there interaction by T2 inflammation, female sex, and obesity?

Study Design and Methods

This is a retrospective cohort study using electronic health record data of patients with asthma followed for at least 1 year in the UCHealth system. The primary outcome was asthma exacerbation rate, defined by the prescription of an oral corticosteroid burst. Predictors of interest included T2 high inflammation, defined as absolute eosinophil count (AEC) ≥ 300 cells/μL, BMI, and sex. Predictors of the numbers of exacerbation and prespecified interactions were identified with negative binomial models. A natural cubic spline was used to model the dose response between AEC and exacerbation rate.

Results

The cohort included 70,939 patients with asthma; 52% had T2 high inflammation and 62% were female, with 70% of patients being overweight or obese. Individuals with T2 high inflammation had higher adjusted rates of exacerbation (adjusted incidence rate ratio, 1.13; 95% CI, 1.10-1.16). AEC predicted exacerbation frequency in a dose-dependent manner. There was significant effect modification by sex, with female participants with T2 high inflammation having increased exacerbation rates compared with male participants with T2 high inflammation.

Interpretation

This study finds an increase in exacerbation rate among patients with T2 high inflammation with asthma and shows a dose-dependent response to AEC. To our knowledge, this is the first study to find effect modification by sex and T2 status, identifying a group of patients who could potentially benefit from T2-targeted biologic therapy to decrease their exacerbation rate.
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