Small Airways in Idiopathic Pulmonary Fibrosis: Quiet but Not Forgotten.
作者信息
Maher Toby M
机构信息
Keck School of Medicine University of Southern California, Los Angeles Los Angeles, California.
Interstitial Lung Disease Unit Royal Brompton Hospital London, United Kingdom.
出版信息
Am J Respir Crit Care Med. 2021 Nov 1;204(9):1010-1011. doi: 10.1164/rccm.202108-2007ED.
Abstract
摘要
相似文献
1
Small Airways in Idiopathic Pulmonary Fibrosis: Quiet but Not Forgotten.特发性肺纤维化中的小气道：安静但未被遗忘。
Am J Respir Crit Care Med. 2021 Nov 1;204(9):1010-1011. doi: 10.1164/rccm.202108-2007ED.
2
Increased Airway Wall Thickness in Interstitial Lung Abnormalities and Idiopathic Pulmonary Fibrosis.间质性肺异常和特发性肺纤维化中气道壁厚度增加。
Ann Am Thorac Soc. 2019 Apr;16(4):447-454. doi: 10.1513/AnnalsATS.201806-424OC.
3
[Normal lung volumes in patients with idiopathic pulmonary fibrosis and emphysema].[特发性肺纤维化和肺气肿患者的正常肺容积]
Medicina (B Aires). 2008;68(4):282-4.
4
Occurrence of idiopathic pulmonary fibrosis during immunosuppressive treatment: a case report.免疫抑制治疗期间特发性肺纤维化的发生：一例报告
J Med Case Rep. 2016 May 25;10:127. doi: 10.1186/s13256-016-0916-5.
5
Comment on: CT analysis of the effect of pirfenidone in patients with idiopathic pulmonary fibrosis.关于《吡非尼酮对特发性肺纤维化患者疗效的CT分析》的评论
Eur J Radiol. 2014 Oct;83(10):1988-9. doi: 10.1016/j.ejrad.2014.07.007. Epub 2014 Jul 18.
6
Activated MCTC mast cells infiltrate diseased lung areas in cystic fibrosis and idiopathic pulmonary fibrosis.活化的 MCTC 肥大细胞浸润囊性纤维化和特发性肺纤维化的病变肺区。
Respir Res. 2011 Oct 20;12(1):139. doi: 10.1186/1465-9921-12-139.
7
Increased volume of conducting airways in idiopathic pulmonary fibrosis is independent of disease severity: a volumetric capnography study.特发性肺纤维化中传导气道容积增加与疾病严重程度无关：一项容量式二氧化碳描记法研究
J Breath Res. 2016 Feb 1;10(1):016005. doi: 10.1088/1752-7155/10/1/016005.
8
Diagnosing idiopathic pulmonary fibrosis: Has the time for surgical lung biopsy passed?
Respirology. 2020 Nov;25(11):1112-1113. doi: 10.1111/resp.13909. Epub 2020 Jul 9.
9
Lung Ultrasonography in Patients With Idiopathic Pulmonary Fibrosis: Evaluation of a Simplified Protocol With High-Resolution Computed Tomographic Correlation.特发性肺纤维化患者的肺部超声检查：一项与高分辨率计算机断层扫描相关性的简化方案评估
J Ultrasound Med. 2018 Mar;37(3):689-696. doi: 10.1002/jum.14406. Epub 2017 Sep 6.
10
[Nutrition in idiopathic pulmonary fibrosis: The great forgotten?].
Medicina (B Aires). 2021;81(4):671-673.
引用本文的文献
1
A Multimodal Spatial and Epigenomic Atlas of Human Adult Lung Topography.人类成年肺脏拓扑结构的多模态空间与表观基因组图谱
bioRxiv. 2025 May 23:2025.05.23.655666. doi: 10.1101/2025.05.23.655666.
2
Oscillometry Assesses Small Airway Disease and Reveals Peripheral Lung Pathology in Early Pulmonary Fibrosis: A Cross-Sectional Study.振荡法评估早期肺纤维化中的小气道疾病并揭示外周肺病理：一项横断面研究
Diagnostics (Basel). 2024 Dec 20;14(24):2873. doi: 10.3390/diagnostics14242873.
3
May Small Airways Dysfunction (SAD) Play a Role in the Idiopathic Pulmonary Fibrosis (IPF) and May SAD Be a Therapeutic Target?小气道功能障碍 (SAD) 可能在特发性肺纤维化 (IPF) 中起作用，SAD 是否可能成为治疗靶点？
Adv Respir Med. 2024 Sep 6;92(5):348-355. doi: 10.3390/arm92050033.
4
Microscopic Small Airway Abnormalities Identified in Early Idiopathic Pulmonary Fibrosis Using Endobronchial Optical Coherence Tomography.经支气管光学相干断层成像术在特发性肺纤维化早期识别微观小气道异常。
Am J Respir Crit Care Med. 2024 Aug 15;210(4):473-483. doi: 10.1164/rccm.202401-0249OC.
5
The Role of Small Airway Disease in Pulmonary Fibrotic Diseases.小气道疾病在肺纤维化疾病中的作用。
J Pers Med. 2023 Nov 13;13(11):1600. doi: 10.3390/jpm13111600.
6
Differential Transcriptomic Signatures of Small Airway Cell Cultures Derived from IPF and COVID-19-Induced Exacerbation of Interstitial Lung Disease.特发性肺纤维化和 COVID-19 诱导的间质性肺病加重中小气道细胞培养物的差异转录组特征。
Cells. 2023 Oct 21;12(20):2501. doi: 10.3390/cells12202501.
本文引用的文献
1
Small Airway Reduction and Fibrosis Is an Early Pathologic Feature of Idiopathic Pulmonary Fibrosis.小气道减少和纤维化是特发性肺纤维化的早期病理特征。
Am J Respir Crit Care Med. 2021 Nov 1;204(9):1048-1059. doi: 10.1164/rccm.202103-0585OC.
2
Single-cell RNA-seq reveals ectopic and aberrant lung-resident cell populations in idiopathic pulmonary fibrosis.单细胞 RNA 测序揭示特发性肺纤维化中异位和异常的肺驻留细胞群体。
Sci Adv. 2020 Jul 8;6(28):eaba1983. doi: 10.1126/sciadv.aba1983. eCollection 2020 Jul.
3
Small airways pathology in idiopathic pulmonary fibrosis: a retrospective cohort study.特发性肺纤维化中小气道病变：一项回顾性队列研究。
Lancet Respir Med. 2020 Jun;8(6):573-584. doi: 10.1016/S2213-2600(19)30356-X. Epub 2020 Feb 13.
4
Idiopathic Pulmonary Fibrosis Is a Genetic Disease Involving Mucus and the Peripheral Airways.特发性肺纤维化是一种涉及黏液和外周气道的遗传疾病。
Ann Am Thorac Soc. 2018 Nov;15(Suppl 3):S192-S197. doi: 10.1513/AnnalsATS.201802-144AW.
5
Recent advances in understanding idiopathic pulmonary fibrosis.特发性肺纤维化认识的最新进展
F1000Res. 2016 May 31;5. doi: 10.12688/f1000research.8209.1. eCollection 2016.
6
Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis.全基因组关联研究鉴定出多个肺纤维化易感性位点。
Nat Genet. 2013 Jun;45(6):613-20. doi: 10.1038/ng.2609. Epub 2013 Apr 14.
7
Targeted injury of type II alveolar epithelial cells induces pulmonary fibrosis.靶向损伤 II 型肺泡上皮细胞可诱导肺纤维化。
Am J Respir Crit Care Med. 2010 Feb 1;181(3):254-63. doi: 10.1164/rccm.200810-1615OC. Epub 2009 Oct 22.
8
The lung's "quiet zone".肺部的“安静区域”。
N Engl J Med. 1970 Jun 4;282(23):1318-9. doi: 10.1056/NEJM197006042822311.
9
Pathogenesis of "fibrosis" in interstitial pneumonia: an electron microscopic study.
Hum Pathol. 1985 Oct;16(10):1015-24. doi: 10.1016/s0046-8177(85)80279-3.
10
Relationship of alveolar epithelial injury and repair to the induction of pulmonary fibrosis.肺泡上皮损伤与修复与肺纤维化诱导的关系。
Am J Pathol. 1988 Feb;130(2):377-83.
Zotero 插件