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早期表型分型:慢性阻塞性肺疾病干预的机会。

Early Endotyping: A Chance for Intervention in Chronic Obstructive Pulmonary Disease.

机构信息

1 COPD Program, Lovelace Respiratory Research Institute, Albuquerque, New Mexico.

2 Department of Internal Medicine, University of New Mexico School of Medicine, Albuquerque, New Mexico; and.

出版信息

Am J Respir Cell Mol Biol. 2018 Jul;59(1):13-17. doi: 10.1165/rcmb.2018-0002PS.

Abstract

Chronic obstructive pulmonary disease (COPD) is a syndrome that comprises several lung pathologies, but subphenotyping the various disease subtypes has been difficult. One reason may be that current efforts focused on studying COPD once it has occurred do not allow tracing back to the different origins of disease. This perspective proposes that emphysema originates when susceptible airway, endothelial, and/or hematopoietic cells are exposed to environmental toxins such as cigarette smoke, biomass fuel, or traffic emissions. These susceptible cell types may initiate distinct pathobiological mechanisms ("COPD endotypes") that ultimately manifest the emphysematous destruction of the lung. On the basis of evidence from the "airway" endotype, we suggest that grading these endotypes by severity may allow better diagnosis of disease at early stages when intervention can be designed on the basis of the mechanisms involved. Therefore, genomic, proteomic, and metabolomic studies on at-risk patients will be important in the identification of biomarkers that help designate each endotype. Together with understanding of the involved molecular pathways that lead to disease manifestation, these efforts may lead to development of intervention strategies.

摘要

慢性阻塞性肺疾病(COPD)是一种包含多种肺部病理的综合征,但对各种疾病亚型进行亚表型分析一直很困难。原因之一可能是,目前针对 COPD 的研究重点是在疾病已经发生之后进行,而无法追溯到疾病的不同起源。这种观点认为,当易感气道、内皮和/或造血细胞暴露于环境毒素(如香烟烟雾、生物质燃料或交通排放物)时,就会引发肺气肿。这些易感细胞类型可能引发不同的病理生物学机制(“COPD 表型”),最终导致肺部的气肿性破坏。基于“气道”表型的证据,我们建议通过严重程度对这些表型进行分级,以便在可以根据涉及的机制进行干预的早期阶段更好地诊断疾病。因此,对高危患者进行基因组、蛋白质组和代谢组学研究对于确定有助于指定每个表型的生物标志物将非常重要。此外,对导致疾病表现的相关分子途径的了解,可能会为干预策略的制定提供指导。

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