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Relationship between age and bronchodilator response at diagnosis in adult-onset asthma

机译:成人发病哮喘诊断年龄与支气管扩张剂反应的关系

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BACKGROUND:Possible variation in bronchodilator response (BDR) according to age at the diagnosis of adult-onset asthma is unknown. Our aim was to assess if BDR in FEV 1 is related to age at diagnosis of adult-onset asthma and how many subjects fulfill the 400?mL criterion of BDR, the suggested cut-off for asthma-like reversibility in asthma-COPD overlap (ACO).METHODS:A total of 1030 patients with adult-onset asthma were included; 245 from SAAS (Sein?joki Adult Asthma Study, Finland) and 785 from COREA (Cohort for Reality and Evolution of Adult Asthma in Korea) cohorts. BDR in FEV 1 at the diagnosis of asthma was assessed. Patients were divided into groups based on age at asthma diagnosis: ?40, 40-59.9, and?≥?60?years. The cohorts were analyzed separately.RESULTS:BDR % in FEV 1 did not differ between the groups of different age at asthma diagnosis and no correlation between BDR and age was found. Of patients aged ≥40?years, only 18% (SAAS-cohort) and 5% (COREA-cohort) reached the 400?mL BDR in FEV 1 . After exclusion of possible ACO patients, the results remained similar.CONCLUSION:By using two large cohorts of steroid-naive patients with asthma, we have shown that BDR at diagnosis of asthma is constant over large age span range, and the limit of 400?mL in BDR in FEV 1 is rarely reached.TRIAL REGISTRATION:Sein?joki Adult Asthma Study is registered at ClinicalTrials.gov with identifier number NCT02733016 .
机译:背景:根据成人发作哮喘诊断的年龄的核糖助剂(BDR)可能的变化是未知的。我们的目的是评估FEV1中的BDR是否与诊断成人发作哮喘的年龄相关,并且有多少受试者满足BDR的400?ML标准,在哮喘 - COPD重叠中的哮喘般的可逆性建议的截止值( ACO)。方法:共有1030例成人发病哮喘; 245来自SaaS(Sein?Joki成人哮喘学习,芬兰)和来自Corea(韩国成人哮喘的现实和演变的队列)的队列。评估FEV 1的BDR在哮喘的诊断中进行了评估。患者分为基于哮喘诊断的年龄的群体:<?40,40-59.9,≥?60?年。分别分析群组。结果:FEV 1中的BDR%在哮喘诊断中不同年龄的组之间没有差异,发现BDR和年龄之间没有相关性。 ≥40岁的患者患者,只有18%(SaaS-Cohort)和5%(Corea-Cohort)在FEV 1中达到400?ML BDR。排除可能的ACO患者后,结果仍然相似。结论:通过使用两个大群体的哮喘患者的类固醇 - 天真患者,我们已经表明,哮喘诊断的BDR在大年龄跨度范围内恒定,并且限制为400? ML在FEV 1中的BDR中很少达到.Tial注册:Sein?Joki成年人哮喘学习在ClinicalTrials.gov中注册了NCT02733016。

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