Computed tomography morphological assessments of central airways in interstitial lung abnormalities and idiopathic pulmonary fibrosis.

IF 5.8 2区 医学 Q1 Medicine Respiratory Research Pub Date : 2024-11-10 DOI:10.1186/s12931-024-03032-5
Tomoki Maetani, Naoya Tanabe, Kiminobu Tanizawa, Ryo Sakamoto, Yusuke Shiraishi, Yusuke Hayashi, Michihiro Uyama, Atsushi Matsunashi, Susumu Sato, Katsuhiro Suzuki, Izuru Masuda, Motonari Fukui, Shizuo Kaji, Tomohiro Handa, Toyohiro Hirai
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Abstract

Background: Little is known about whether central airway morphological changes beyond traction bronchiectasis develop and affect clinical outcomes in patients with idiopathic pulmonary fibrosis (IPF). This study aimed to compare central airway structure comprehensively between patients with IPF, subjects with interstitial lung abnormality (ILA), and those without ILA (control) using computed tomography (CT). We further examined the prognostic impact of IPF-specific CT airway parameters in patients with IPF.

Methods: This retrospective study included male patients with IPF, and male health checkup subjects divided into those with ILA and control based on lung cancer screening CT. Using an artificial intelligence-based segmentation technique, the extent of fibrotic regions in the lung was quantified. After airway tree segmentation, CT parameters for central airway morphology, including the lumen area of the extrapulmonary airways (LAextra), wall and lumen area of the segmental/subsegmental intrapulmonary airways (WAintra and LAintra), tracheal distortion (tortuosity and curvature) and bifurcation angle of the main carina, were calculated.

Results: There were 106 patients with IPF, 53 subjects with ILA, and 1295 controls. Multivariable models adjusted for age, height and smoking history revealed that LAintra and WAintra were larger in both ILA and IPF, and that tracheal tortuosity and curvature were higher in IPF, but not in ILA, than in the control, whereas the bifurcation angle did not differ between the 3 groups. According to multivariable Cox proportional hazards models including only patients with IPF, increased WAintra was significantly associated with greater mortality (standardized hazard ratio [95% confidence interval] = 1.58 [1.17, 2.14]), independent of the volume of fibrotic regions, normal-appearing regions, or the whole airway tree in the lung.

Conclusion: Increased lumen area and wall thickening of the central airways may be involved in the pathogenesis of ILA and IPF, and wall thickening may affect the prognosis of patients with IPF.

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对肺间质异常和特发性肺纤维化的中央气道进行计算机断层扫描形态学评估。
背景:对于特发性肺纤维化(IPF)患者除牵引性支气管扩张外是否还会发生中心气道形态学改变并影响临床预后,目前所知甚少。本研究旨在使用计算机断层扫描(CT)全面比较 IPF 患者、肺间质异常(ILA)患者和无 ILA 患者(对照组)的中心气道结构。我们进一步研究了 IPF 特异性 CT 气道参数对 IPF 患者预后的影响:这项回顾性研究包括 IPF 男性患者,以及根据肺癌筛查 CT 将 ILA 患者和对照组分为两组的男性健康体检者。采用基于人工智能的分割技术,对肺部纤维化区域的范围进行量化。气道树分割后,计算中央气道形态的CT参数,包括肺外气道的管腔面积(LAextra)、肺内气道节段/亚节段的管壁和管腔面积(WAintra和LAintra)、气管变形(迂曲度和弯曲度)以及主心尖的分叉角:共有 106 名 IPF 患者、53 名 ILA 患者和 1295 名对照者。根据年龄、身高和吸烟史调整的多变量模型显示,ILA 和 IPF 患者的 LAintra 和 WAintra 均较大,IPF 患者的气管迂曲度和弯曲度高于对照组,但 ILA 患者的气管迂曲度和弯曲度不高于对照组,而 3 组患者的分叉角没有差异。根据仅包括IPF患者的多变量Cox比例危险模型,WAintra增加与死亡率升高显著相关(标准化危险比[95%置信区间] = 1.58 [1.17,2.14]),与纤维化区域、外观正常区域或肺部整个气道树的体积无关:结论:中心气道管腔面积增大和管壁增厚可能与 ILA 和 IPF 的发病机制有关,管壁增厚可能会影响 IPF 患者的预后。
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来源期刊
Respiratory Research
Respiratory Research RESPIRATORY SYSTEM-
CiteScore
9.70
自引率
1.70%
发文量
314
审稿时长
4-8 weeks
期刊介绍: Respiratory Research publishes high-quality clinical and basic research, review and commentary articles on all aspects of respiratory medicine and related diseases. As the leading fully open access journal in the field, Respiratory Research provides an essential resource for pulmonologists, allergists, immunologists and other physicians, researchers, healthcare workers and medical students with worldwide dissemination of articles resulting in high visibility and generating international discussion. Topics of specific interest include asthma, chronic obstructive pulmonary disease, cystic fibrosis, genetics, infectious diseases, interstitial lung diseases, lung development, lung tumors, occupational and environmental factors, pulmonary circulation, pulmonary pharmacology and therapeutics, respiratory immunology, respiratory physiology, and sleep-related respiratory problems.
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