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肺动脉高压的病理学和病理生物学:现状和研究展望。

Pathology and pathobiology of pulmonary hypertension: state of the art and research perspectives.

机构信息

Faculté de Médecine, Université Paris-Sud and Université Paris-Saclay, Le Kremlin-Bicêtre, France.

INSERM UMR_S 999, Le Plessis-Robinson, France.

出版信息

Eur Respir J. 2019 Jan 24;53(1). doi: 10.1183/13993003.01887-2018. Print 2019 Jan.

Abstract

Clinical and translational research has played a major role in advancing our understanding of pulmonary hypertension (PH), including pulmonary arterial hypertension and other forms of PH with severe vascular remodelling ( chronic thromboembolic PH and pulmonary veno-occlusive disease). However, PH remains an incurable condition with a high mortality rate, underscoring the need for a better transfer of novel scientific knowledge into healthcare interventions. Herein, we review recent findings in pathology (with the questioning of the strict morphological categorisation of various forms of PH into pre- or post-capillary involvement of pulmonary vessels) and cellular mechanisms contributing to the onset and progression of pulmonary vascular remodelling associated with various forms of PH. We also discuss ways to improve management and to support and optimise drug development in this research field.

摘要

临床和转化研究在推进我们对肺动脉高压(PH)的认识方面发挥了重要作用,包括肺动脉高压和其他严重血管重塑形式的 PH(慢性血栓栓塞性 PH 和肺静脉闭塞性疾病)。然而,PH 仍然是一种无法治愈的疾病,死亡率很高,这突显了将新的科学知识更好地转化为医疗保健干预措施的必要性。在此,我们回顾了病理学的最新发现(质疑将各种形式的 PH 严格地按照肺血管的前或后毛细血管受累进行形态分类)和导致与各种形式的 PH 相关的肺血管重塑发生和进展的细胞机制。我们还讨论了改善该研究领域的管理以及支持和优化药物开发的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81ea/6351340/1fdc1d44c0d5/ERJ-01887-2018.01.jpg

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