Department of Respiratory and Critical Care Medicine, Shanghai Pulmonary Hospital, Institute of Respiratory Medicine, Tongji University School of Medicine, 507 Zhengmin Road, Shanghai, 200433, China.
State Key Laboratory of Respiratory Disease, National Clinical Research Center for Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.
Respir Res. 2022 Dec 3;23(1):328. doi: 10.1186/s12931-022-02254-9.
Bronchiectasis is a highly heterogeneous chronic airway disease with marked geographic and ethnic variations. Most influential cohort studies to date have been performed in Europe and USA, which serve as the examples for developing a cohort study in China where there is a high burden of bronchiectasis. The Establishment of China Bronchiectasis Registry and Research Collaboration (BE-China) is designed to: (1) describe the clinical characteristics and natural history of bronchiectasis in China and identify the differences of bronchiectasis between the western countries and China; (2) identify the risk factors associated with disease progression in Chinese population; (3) elucidate the phenotype and endotype of bronchiectasis by integrating the genome, microbiome, proteome, and transcriptome with detailed clinical data; (4) facilitate large randomized controlled trials in China.
The BE-China is an ongoing prospective, longitudinal, multi-center, observational cohort study aiming to recruit a minimum of 10,000 patients, which was initiated in January 2020 in China. Comprehensive data, including medical history, aetiological testing, lung function, microbiological profiles, radiological scores, comorbidities, mental status, and quality of life (QoL), will be collected at baseline. Patients will be followed up annually for up to 10 years to record longitudinal data on outcomes, treatment patterns and QoL. Biospecimens, if possible, will be collected and stored at - 80 °C for further research. Up to October 2021, the BE-China has enrolled 3758 patients, and collected 666 blood samples and 196 sputum samples from 91 medical centers. The study protocol has been approved by the Shanghai Pulmonary Hospital ethics committee, and all collaborating centers have received approvals from their local ethics committee. All patients will be required to provide written informed consent to their participation.
Findings of the BE-China will be crucial to reveal the clinical characteristics and natural history of bronchiectasis and facilitate evidence-based clinical practice in China. Trial registration Registration Number in ClinicalTrials.gov: NCT03643653.
支气管扩张症是一种高度异质性的慢性气道疾病,具有明显的地域和种族差异。迄今为止,最有影响力的队列研究都集中在欧洲和美国,这些国家为中国开展队列研究提供了范例,中国的支气管扩张症负担很重。中国支气管扩张症注册和研究协作组(BE-China)旨在:(1)描述中国支气管扩张症的临床特征和自然史,并确定西方国家和中国之间支气管扩张症的差异;(2)确定与中国人群疾病进展相关的危险因素;(3)通过整合基因组、微生物组、蛋白质组和转录组与详细的临床数据,阐明支气管扩张症的表型和内型;(4)促进中国的大型随机对照试验。
BE-China 是一项正在进行的前瞻性、纵向、多中心、观察性队列研究,旨在招募至少 10000 名患者,于 2020 年 1 月在中国启动。将收集包括病史、病因学检测、肺功能、微生物谱、放射学评分、合并症、精神状态和生活质量(QoL)在内的综合数据。患者将每年进行随访,最长可达 10 年,以记录结局、治疗模式和 QoL 的纵向数据。如果可能,将收集并储存生物标本在-80°C 用于进一步研究。截至 2021 年 10 月,BE-China 已招募 3758 名患者,从 91 家医疗中心收集了 666 份血液样本和 196 份痰液样本。该研究方案已获得上海肺科医院伦理委员会的批准,所有合作中心均已获得其当地伦理委员会的批准。所有患者都需要提供书面知情同意书才能参与。
BE-China 的研究结果对于揭示支气管扩张症的临床特征和自然史,促进中国循证临床实践至关重要。
ClinicalTrials.gov 注册号:NCT03643653。