Department of Respiratory Medicine, Copenhagen University Hospital - Hvidovre, Hvidovre, Denmark.
Division of Pulmonary and Sleep Medicine, Children's National Health System, Washington DC, USA.
Respir Med. 2024 Nov-Dec;234:107808. doi: 10.1016/j.rmed.2024.107808. Epub 2024 Sep 14.
Phenotype classification contributes to risk assessment of asthma. Previous studies have applied this concept primarily to adult populations and in the setting of research protocol assessments which may not be applicable to clinical settings.
Exploring the value of routinely collected clinical data for phenotype classification and risk assessment of childhood asthma.
Using hospital and laboratory data, 29,851 children in a Danish nationwide database aged 2-17 years with ICS-treated asthma in 2015 followed for two years (730 days) were classified to have T2 (elevated blood eosinophils (>300 cells/μL) and/or elevated total- or specific-IgE), and/or non-T2 risk factors (in utero tobacco exposure and/or severe viral infections). Logistic regression was applied to quantify associations of risk factors with asthma severity, control, and exacerbation risk.
In a complete case analysis, 85.8 % children had at least one T2 risk factor and 29.3 % had mixed T2/non-T2 risk factors. Elevated blood eosinophils and total/specific IgE were associated with exacerbations (ORs 1.55 (1.38-1.73) and 1.41 (1.20-1.66) and higher asthma severity (1.42 (1.24-1.63) and 1.31 (1.08-1.60)), respectively. Dose-dependency was observed between blood eosinophil counts, total IgE levels, and risk of adverse outcomes. Furthermore, accumulation of risk factors demonstrated an increasing risk, with children with all four risk factors having a high risk of any adverse asthma-related outcome (OR 3.13 (2.03-4.82) CONCLUSION: Asthma phenotypic markers defined in research protocols can be reliably applied in real-world settings by utilizing data collected during routine clinical care and enable better classification of risk of adverse asthma outcomes.
表型分类有助于评估哮喘风险。既往研究主要应用于成年人群,以及在研究方案评估中,而这些方法可能不适用于临床环境。
探索常规临床数据在儿童哮喘表型分类和风险评估中的价值。
利用丹麦全国性数据库中的医院和实验室数据,对 2015 年接受 ICS 治疗的 2-17 岁哮喘患儿(29851 例)进行了为期两年(730 天)的随访,根据患儿是否存在 T2(血嗜酸性粒细胞升高(>300 个/μL)和/或总 IgE 或特异性 IgE 升高)和/或非 T2 危险因素(宫内烟草暴露和/或严重病毒感染)进行分类。采用逻辑回归量化危险因素与哮喘严重程度、控制情况和加重风险的相关性。
在完整病例分析中,85.8%的患儿至少存在 1 项 T2 危险因素,29.3%的患儿存在 T2/非 T2 混合危险因素。血嗜酸性粒细胞和总/特异性 IgE 与哮喘加重(OR 1.55[1.38-1.73]和 1.41[1.20-1.66])和更高的哮喘严重程度(OR 1.42[1.24-1.63]和 1.31[1.08-1.60])相关。血嗜酸性粒细胞计数、总 IgE 水平与不良结局风险之间存在剂量依赖性。此外,危险因素的累积显示出风险的增加,具有全部 4 项危险因素的患儿发生任何不良哮喘相关结局的风险很高(OR 3.13[2.03-4.82])。
通过利用常规临床护理期间收集的数据,可在真实环境中可靠地应用研究方案中定义的哮喘表型标志物,从而更好地对不良哮喘结局风险进行分类。