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美国胸科学会官方研讨会报告:罕见呼吸系统疾病的转化研究。

An Official American Thoracic Society Workshop Report: Translational Research in Rare Respiratory Diseases.

出版信息

Ann Am Thorac Soc. 2017 Aug;14(8):1239-1247. doi: 10.1513/AnnalsATS.201705-406WS.

Abstract

Rare respiratory diseases (RRDs) are a heterogeneous group of disorders that collectively represent a significant health care burden. In recent years, strong advocacy and policy initiatives have led to advances in the implementation of research and clinical care for rare diseases. The development of specialized centers and research networks has facilitated support for affected individuals as well as emerging programs in basic, translational, and clinical research. In selected RRDs, subsequent gains in knowledge have informed the development of targeted therapies and effective diagnostic tests, but many gaps persist. There was therefore a desire to identify the elements contributing to an effective translational research program in RRDs. To this end, a workshop was convened in October 2015 with a focus on the implementation of effective transnational research networks and collaborations aimed at developing novel diagnostic and therapeutic tools. Key elements included an emphasis on molecular pathogenesis, the continuing engagement of patient advocacy groups and policy makers, the effective use of preclinical models in the translational research pipeline, and the detailed phenotyping of patient cohorts. During the course of the workshop, current logistical and knowledge gaps were identified, and new solutions or opportunities were highlighted.

摘要

罕见呼吸系统疾病(RRDs)是一组异质性疾病,它们共同构成了重大的医疗保健负担。近年来,强有力的宣传和政策举措推动了罕见病研究和临床护理的实施进展。专门中心和研究网络的发展为受影响的个人提供了支持,并为基础、转化和临床研究中的新兴项目提供了支持。在某些罕见呼吸系统疾病中,随后的知识进步为靶向治疗和有效诊断测试的开发提供了信息,但仍存在许多空白。因此,人们希望确定有助于罕见呼吸系统疾病有效转化研究计划的要素。为此,2015 年 10 月举办了一次研讨会,重点是实施有效的跨国研究网络和合作,旨在开发新的诊断和治疗工具。关键要素包括强调分子发病机制、持续让患者权益倡导团体和政策制定者参与、在转化研究管道中有效利用临床前模型,以及对患者队列进行详细表型分析。在研讨会期间,确定了当前的后勤和知识差距,并突出了新的解决方案或机会。

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