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系统医学在间质性肺疾病中的进展。

Systems medicine advances in interstitial lung disease.

机构信息

Comprehensive Pneumology Center, Ludwig-Maximilians-Universität, University Hospital Grosshadern and Helmholtz Zentrum München and Member of the German Center for Lung Research, Munich, Germany.

Division of Respiratory Sciences and Critical Care Medicine, Dept of Medicine, University of Colorado, Denver, CO, USA.

出版信息

Eur Respir Rev. 2017 Sep 27;26(145). doi: 10.1183/16000617.0021-2017. Print 2017 Sep 30.

DOI:10.1183/16000617.0021-2017
PMID:28954764
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9488840/
Abstract

Fibrotic lung diseases involve subject-environment interactions, together with dysregulated homeostatic processes, impaired DNA repair and distorted immune functions. Systems medicine-based approaches are used to analyse diseases in a holistic manner, by integrating systems biology platforms along with clinical parameters, for the purpose of understanding disease origin, progression, exacerbation and remission.Interstitial lung diseases (ILDs) refer to a heterogeneous group of complex fibrotic diseases. The increase of systems medicine-based approaches in the understanding of ILDs provides exceptional advantages by improving diagnostics, unravelling phenotypical differences, and stratifying patient populations by predictable outcomes and personalised treatments. This review discusses the state-of-the-art contributions of systems medicine-based approaches in ILDs over the past 5 years.

摘要

纤维化肺疾病涉及宿主-环境相互作用,以及失调的内稳态过程、受损的 DNA 修复和紊乱的免疫功能。基于系统医学的方法用于全面分析疾病,通过整合系统生物学平台以及临床参数,以了解疾病的起源、进展、恶化和缓解。间质性肺疾病(ILDs)是指一组异质性的复杂纤维化疾病。基于系统医学的方法在ILDs 中的应用增加,通过提高诊断能力、揭示表型差异以及通过可预测的结果和个体化治疗对患者人群进行分层,提供了卓越的优势。这篇综述讨论了过去 5 年来基于系统医学的方法在 ILDs 中的最新进展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8854/9488840/a7819dd3eb85/ERR-0021-2017.01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8854/9488840/a7819dd3eb85/ERR-0021-2017.01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8854/9488840/a7819dd3eb85/ERR-0021-2017.01.jpg

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Am J Respir Crit Care Med. 2017 Jul 15;196(2):208-219. doi: 10.1164/rccm.201607-1525OC.
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iTRAQ-Based Proteomics Reveals Novel Biomarkers for Idiopathic Pulmonary Fibrosis.基于iTRAQ的蛋白质组学揭示特发性肺纤维化的新型生物标志物。
PLoS One. 2017 Jan 25;12(1):e0170741. doi: 10.1371/journal.pone.0170741. eCollection 2017.
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Host-Microbial Interactions in Idiopathic Pulmonary Fibrosis.特发性肺纤维化中的宿主-微生物相互作用
Am J Respir Crit Care Med. 2017 Jun 15;195(12):1640-1650. doi: 10.1164/rccm.201607-1408OC.
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Single-cell RNA sequencing identifies diverse roles of epithelial cells in idiopathic pulmonary fibrosis.单细胞 RNA 测序鉴定特发性肺纤维化中上皮细胞的多种作用。
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Six-SOMAmer Index Relating to Immune, Protease and Angiogenic Functions Predicts Progression in IPF.与免疫、蛋白酶和血管生成功能相关的六SOMAmer指数可预测特发性肺纤维化的病情进展。
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Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia.全基因组归因研究确定了肺纤维化的新HLA基因座以及自身免疫在特发性间质性肺炎纤维化中的潜在作用。
BMC Genet. 2016 Jun 7;17(1):74. doi: 10.1186/s12863-016-0377-2.
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Integrated Genomics Reveals Convergent Transcriptomic Networks Underlying Chronic Obstructive Pulmonary Disease and Idiopathic Pulmonary Fibrosis.整合基因组学揭示慢性阻塞性肺疾病和特发性肺纤维化潜在的趋同转录组网络。
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Comparative proteomic analysis of bronchoalveolar lavage of familial and sporadic cases of idiopathic pulmonary fibrosis.家族性和散发性特发性肺纤维化病例支气管肺泡灌洗的比较蛋白质组学分析
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