Protocol and research program of the European registry and biobank for interstitial lung diseases (eurILDreg).

IF 2.6 3区 医学 Q2 RESPIRATORY SYSTEM
Ekaterina Krauss, Silke Tello, Jennifer Naumann, Sandra Wobisch, Clemens Ruppert, Stefan Kuhn, Poornima Mahavadi, Raphael W Majeed, Philippe Bonniaud, Maria Molina-Molina, Athol Wells, Nik Hirani, Carlo Vancheri, Simon Walsh, Matthias Griese, Bruno Crestani, Andreas Guenther
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引用次数: 0

Abstract

Background and aims: Interstitial lung diseases (ILDs), encompassing both pediatric and adult cases, present a diverse spectrum of chronic conditions with variable prognosis. Despite limited therapeutic options beyond antifibrotic drugs and immunosuppressants, accurate diagnosis is challenging, often necessitating invasive procedures that may not be feasible for certain patients. Drawn against this background, experts across pediatric and adult ILD fields have joined forces in the RARE-ILD initiative to pioneer novel non-invasive diagnostic algorithms and biomarkers. Collaborating with the RARE-ILD consortium, the eurILDreg aims to comprehensively describe different ILDs, analyze genetically defined forms across age groups, create innovative diagnostic and therapeutic biomarkers, and employ artificial intelligence for data analysis.

Methods: The foundation of eurILDreg is built on a comprehensive parameter list developed and adopted by clinical experts, encompassing over 1,800 distinct parameters related to patient history, clinical examinations, diagnosis, lung function and biospecimen collection. This robust dataset is further enriched with daily assessments captured through the patientMpower app, including handheld spirometry and exercise tests, conducted on approximately 350 patients over the course of a year. This approach involves app-based daily assessments of quality of life, symptom tracking, handheld spirometry, saturation measurement, and the 1-min sit-to-stand test (1-STST). Additionally, pediatric data from the ChILD-EU registry will be integrated into the RARE-ILD Data Warehouse, with the ultimate goal of including a total of 4.000 ILD patients and over 100.000 biospecimen.

Discussion: The collaborative efforts within the consortium are poised to streamline research endeavors significantly, promising to advance patient-centered care, foster innovation, and shape the future landscape of interstitial lung disease research and healthcare practices.

Trial registration: EurILDreg is registered in the German Clinical Trials Register (DRKS 00028968, 26.07.2022), and eurIPFreg is registered in ClinicalTrials.gov (NCT02951416).

欧洲间质性肺病登记和生物库(eurILDreg)的协议和研究计划。
背景和目的:间质性肺疾病(ILDs)包括儿童和成人病例,是一种预后各异的慢性疾病。尽管除抗纤维化药物和免疫抑制剂外,治疗方案有限,但准确诊断仍具有挑战性,往往需要进行侵入性手术,而这对某些患者来说可能并不可行。在此背景下,儿科和成人 ILD 领域的专家们在 RARE-ILD 计划中携手合作,开创了新型非侵入性诊断算法和生物标志物。eurILDreg 与 RARE-ILD 联盟合作,旨在全面描述不同的 ILD,分析各年龄组的基因定义形式,创建创新的诊断和治疗生物标记物,并采用人工智能进行数据分析:eurILDreg 的基础是由临床专家开发和采用的综合参数列表,其中包括与患者病史、临床检查、诊断、肺功能和生物样本采集相关的 1800 多个不同参数。通过 patientMpower 应用程序采集的日常评估进一步丰富了这一强大的数据集,这些评估包括手持式肺活量测定和运动测试,在一年的时间里对大约 350 名患者进行了评估。这种方法包括基于应用程序的生活质量日常评估、症状跟踪、手持式肺活量测量、饱和度测量和 1 分钟坐立测试 (1-STST)。此外,ChILD-EU登记处的儿科数据也将纳入RARE-ILD数据仓库,最终目标是纳入4000名ILD患者和10万多份生物样本:讨论:联盟内的合作努力将大大简化研究工作,有望推动以患者为中心的护理,促进创新,并塑造间质性肺病研究和医疗实践的未来前景:EurILDreg已在德国临床试验注册中心注册(DRKS 00028968, 26.07.2022),eurIPFreg已在ClinicalTrials.gov注册(NCT02951416)。
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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来源期刊
BMC Pulmonary Medicine
BMC Pulmonary Medicine RESPIRATORY SYSTEM-
CiteScore
4.40
自引率
3.20%
发文量
423
审稿时长
6-12 weeks
期刊介绍: BMC Pulmonary Medicine is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of pulmonary and associated disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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