Variables predicting clinical remission among adults with severe asthma treated with biologic agents.

IF 2.6 Q2 ALLERGY
S Yeşilkaya, K Aksu, G Tuğçe Vural Solak, O Akkale, O Telli, H C Tuğlu, G Köycü Buhari, S N Bahçecioğlu, S Demir
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Abstract

Summary: Background. Although biologic agents promise a short- to medium-term remission in asthma, it is unclear whether they can fundamentally alter disease course and achieve long-term remission. We aimed to investigate the clinical remission success of biologics in patients with severe asthma and the factors associated with remission. Methods. Adults followed-up due to severe asthma who were treated with mepolizumab or omalizumab were included in the study. Sociodemographic and clinical characteristics were reviewed. Subjects with and without clinical remission at 12 and 36 months were identified. Comparisons between the groups were made with univariate and multivariable analyses. Results. Seventy-four patients were included in the study. The mean age of subjects was 51.85 (standard deviation: 11.43) years, and 50 (67.57%) were females. The 12- and 36-month remission rates were 72.97% and 51.79%, respectively. Patients with and without remission were similar in terms of age and gender distribution. FEV1% predicted (p = 0.009) and FEV1/FVC ratio (p = 0.039) were significantly higher in those with remission at 12 months compared to those without. FEV1 (p less than 0.001), FEV1% predicted (p less than 0.001) and FEV1/FVC ratio (p = 0.004) were significantly higher in those with remission at 36 months compared to those without. Multivariable logistic regression revealed that higher FEV1% predicted was the only factor independently associated with remission for both time points. Conclusions. Omalizumab and mepolizumab provide significant clinical remission rates in severe asthma. FEV1% predicted is a variable that can independently predict clinical remission among severe asthmatics receiving biologic agents.

预测接受生物制剂治疗的成人重症哮喘患者临床缓解的变量。
摘要:背景。尽管生物制剂有望在中短期内缓解哮喘,但它们能否从根本上改变病程并实现长期缓解尚不清楚。我们旨在研究生物制剂在重症哮喘患者中的临床缓解成功率以及与缓解相关的因素。方法。研究纳入了因重症哮喘接受甲泼尼单抗或奥马珠单抗治疗的随访成人。研究人员回顾了社会人口学和临床特征。确定了在 12 个月和 36 个月时有临床缓解和无临床缓解的受试者。通过单变量和多变量分析对两组患者进行比较。研究结果研究共纳入 74 名患者。受试者的平均年龄为 51.85 岁(标准差:11.43),其中 50 人为女性(67.57%)。12个月和36个月的缓解率分别为72.97%和51.79%。缓解和未缓解患者的年龄和性别分布相似。与未缓解者相比,12 个月后缓解者的预测 FEV1% (p = 0.009) 和 FEV1/FVC 比值 (p = 0.039) 明显更高。与未缓解者相比,36 个月时缓解者的 FEV1(p 小于 0.001)、预测 FEV1% (p 小于 0.001)和 FEV1/FVC 比值(p = 0.004)明显更高。多变量逻辑回归显示,预测 FEV1% 较高是唯一与两个时间点的缓解率独立相关的因素。结论奥马珠单抗和美泊珠单抗可显著提高重症哮喘患者的临床缓解率。FEV1%预测值是一个可以独立预测接受生物制剂治疗的重症哮喘患者临床缓解情况的变量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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