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职业和环境暴露在特发性肺纤维化发病机制中的作用:一项叙述性文献综述

The Role of Occupational and Environmental Exposures in the Pathogenesis of Idiopathic Pulmonary Fibrosis: A Narrative Literature Review.

作者信息

Trethewey Samuel P, Walters Gareth I

机构信息

Respiratory Medicine, University Hospitals Birmingham NHS Foundation Trust, Birmingham B95SS, UK.

Birmingham Regional NHS Occupational Lung Disease Service, Birmingham Chest Clinic, Birmingham B33HX, UK.

出版信息

Medicina (Kaunas). 2018 Dec 10;54(6):108. doi: 10.3390/medicina54060108.

DOI:10.3390/medicina54060108
PMID:30544758
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6306764/
Abstract

Idiopathic pulmonary fibrosis (IPF) is a chronic interstitial lung disease characterised by a progressive and irreversible decline in lung function, which is associated with poor long-term survival. The pathogenesis of IPF is incompletely understood. An accumulating body of evidence, obtained over the past three decades, suggests that occupational and environmental exposures may play a role in the development of IPF. This narrative literature review aims to summarise current understanding and the areas of ongoing research into the role of occupational and environmental exposures in the pathogenesis of IPF.

摘要

特发性肺纤维化(IPF)是一种慢性间质性肺疾病,其特征是肺功能进行性且不可逆地下降,这与长期生存率低相关。IPF的发病机制尚未完全明确。过去三十年积累的大量证据表明,职业和环境暴露可能在IPF的发生发展中起作用。本叙述性文献综述旨在总结目前对于职业和环境暴露在IPF发病机制中的作用的认识以及正在进行研究的领域。

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本文引用的文献

1
Diagnosis of Idiopathic Pulmonary Fibrosis in a Possible Usual Interstitial Pneumonia Pattern: a meta-analysis.特发性肺纤维化在可能的寻常型间质性肺炎模式中的诊断:一项荟萃分析。
Sci Rep. 2018 Oct 26;8(1):15886. doi: 10.1038/s41598-018-34230-z.
2
Metal-Induced Pulmonary Fibrosis.金属诱导性肺纤维化。
Curr Environ Health Rep. 2018 Dec;5(4):486-498. doi: 10.1007/s40572-018-0219-7.
3
Impact of Particulate Matter on the Natural History of IPF: A Matter of Concentrations?颗粒物对特发性肺纤维化自然病程的影响:浓度问题?
Chest. 2018 Sep;154(3):726-727. doi: 10.1016/j.chest.2018.05.043.
4
Diagnosis of Idiopathic Pulmonary Fibrosis: Differential Diagnosis.特发性肺纤维化的诊断:鉴别诊断
Med Sci (Basel). 2018 Sep 4;6(3):73. doi: 10.3390/medsci6030073.
5
Diagnosis of Idiopathic Pulmonary Fibrosis. An Official ATS/ERS/JRS/ALAT Clinical Practice Guideline.特发性肺纤维化诊断。美国胸科学会/欧洲呼吸学会/日本呼吸学会/拉丁美洲胸科学会临床实践指南。
Am J Respir Crit Care Med. 2018 Sep 1;198(5):e44-e68. doi: 10.1164/rccm.201807-1255ST.
6
Developmental pathways in the pathogenesis of lung fibrosis.肺纤维化发病机制中的发育途径。
Mol Aspects Med. 2019 Feb;65:56-69. doi: 10.1016/j.mam.2018.08.004. Epub 2018 Aug 23.
7
Idiopathic Pulmonary Fibrosis (IPF): An Overview.特发性肺纤维化(IPF)概述
J Clin Med. 2018 Aug 6;7(8):201. doi: 10.3390/jcm7080201.
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Causes of Pulmonary Fibrosis in the Elderly.老年人肺纤维化的病因。
Med Sci (Basel). 2018 Jul 24;6(3):58. doi: 10.3390/medsci6030058.
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Clinical behaviour of patients exposed to organic dust and diagnosed with idiopathic pulmonary fibrosis.接触有机粉尘并被诊断为特发性肺纤维化的患者的临床行为。
Respirology. 2018 Dec;23(12):1160-1165. doi: 10.1111/resp.13342. Epub 2018 Jun 13.
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Occupational risk factors for idiopathic pulmonary fibrosis in Southern Europe: a case-control study.南欧特发性肺纤维化的职业危险因素:一项病例对照研究。
BMC Pulm Med. 2018 May 21;18(1):75. doi: 10.1186/s12890-018-0644-2.