黎巴嫩严重哮喘患者嗜酸性粒细胞表型的患病率:PREPARE研究的结果

Wajdi Abi Saleh, Zuhair Alameh, Zeina Aoun Bacha, Joudy Bahous, Pierre Bou Khalil, Zahia Chahine, Hassan Chami, Georges Dabar, Hassan Dheiny, Alfred Dib, Dany Farhat, Carla Irani, Georges Juvelekian, Nadim Kanj, Bassam Mansour, Moussa Riachi, Mirna Waked, Mohamad Yassine, Carole Youakim, Salah Zeinedine, Fares Zaitoun
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引用次数: 0

摘要

背景:黎巴嫩嗜酸性粒细胞哮喘的患病率是严重哮喘中最严重的表型之一,目前尚不清楚。本研究旨在确定黎巴嫩严重哮喘患者嗜酸性粒细胞表型(嗜酸性粒细胞计数≥300细胞/mm3)的患病率。方法:PREPARE研究的黎巴嫩分会是一项全国性、多中心、横断面观察性研究。年龄≥12岁的严重哮喘患者在门诊就诊期间被确定并前瞻性纳入,并完成全球哮喘倡议(GINA)哮喘控制问卷评估。从病历中收集患者的健康特征,并采集血样,测定血清IgE水平和血嗜酸性粒细胞计数。结果:共纳入101例重度哮喘患者(平均年龄46.3±17.0岁,女性占73.27%),其中37%为嗜酸性粒细胞表型,67.3%为IgE > 100 IU/mL的特应性表型,25.7%为特应性和嗜酸性粒细胞表型重叠。近80%的患者患有12岁以上的晚发性哮喘,约85%的患者在研究入组前的12个月内至少有一次严重发作。大多数参与者(64.4%)哮喘未控制,24.7%症状部分控制,10.9%症状控制。19.8%的参与者服用慢性口服糖皮质激素,78.2%的参与者服用糖皮质激素短期治疗,所有参与者都服用吸入糖皮质激素和长效β激动剂的联合处方。结论:大多数严重哮喘患者未得到控制,其中37%呈现嗜酸性粒细胞表型,鉴于新的表型特异性治疗方案,应考虑到这一点,以便更好地管理这些患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

PRevalence of the Eosinophilic Phenotype Among SeveRE asthma patients in Lebanon: results of the PREPARE study.

PRevalence of the Eosinophilic Phenotype Among SeveRE asthma patients in Lebanon: results of the PREPARE study.

Background: The prevalence of eosinophilic asthma in Lebanon, one of the most severe phenotypes among severe asthma, is not known. This study aimed at determining the prevalence of the eosinophilic phenotype defined as an eosinophil count ≥ 300 cells/mm3 among severe asthma patients in Lebanon.

Methods: The Lebanese Chapter of the PREPARE study was a national, multicenter, cross-sectional observational study. Patients aged ≥ 12 years with severe asthma were identified and prospectively enrolled during clinic visits and completed the Global Initiative for Asthma (GINA) assessment of asthma control questionnaire. Patients' health characteristics were collected from medical records and blood samples were obtained for measurement of serum IgE levels and blood eosinophils count.

Results: Overall, 101 patients (with mean age of 46.3 ± 17.0 years and 73.27% females) with severe asthma were included and, among them, 37% had eosinophilic phenotype, 67.3% had atopic phenotype with IgE > 100 IU/mL and 25.7% patients had overlapping atopic and eosinophilic phenotypes. Close to 80% had late-onset asthma, beyond 12 years of age, and around 85% had at least one severe exacerbation in the 12 months prior to study enrolment. The majority of participants [64.4%] had uncontrolled asthma, 24.7% had partially controlled symptoms and 10.9% had controlled symptoms. 19.8% of participants were on chronic oral corticosteroids, 78.2% had short course treatment of corticosteroids and all were prescribed a combination of inhaled corticosteroids and long-acting beta-agonist.

Conclusions: The majority of patients with severe asthma were uncontrolled of which 37% present with an eosinophilic phenotype, which should be taken into consideration for better management of these patients in view of the novel phenotype-specific therapeutic options.

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