Suppr超能文献

特发性肺纤维化高分辨率计算机断层扫描特征的定量分析:一项结构-功能相关性研究。

Quantitative analysis of high-resolution computed tomography features of idiopathic pulmonary fibrosis: a structure-function correlation study.

作者信息

Sun Haishuang, Liu Min, Kang Han, Yang Xiaoyan, Zhang Peiyao, Zhang Rongguo, Dai Huaping, Wang Chen

机构信息

Department of Respiratory Medicine, The First Hospital of Jilin University, Changchun, China.

Department of Pulmonary and Critical Care Medicine, China-Japan Friendship Hospital, Beijing, China.

出版信息

Quant Imaging Med Surg. 2022 Jul;12(7):3655-3665. doi: 10.21037/qims-21-1232.

Abstract

BACKGROUND

The quantitative analysis of high-resolution computed tomography (HRCT) is increasingly being used to quantify the severity and evaluate the prognosis of disease. Our aim was to quantify the HRCT features of idiopathic pulmonary fibrosis (IPF) and identify their association with pulmonary function tests.

METHODS

This was a retrospective, single-center, clinical research study. Patients with IPF were retrospectively included. Pulmonary segmentation was performed using the deep learning-based method. Radiologists manually segmented 4 findings of IPF, including honeycombing (HC), reticular pattern (RE), traction bronchiectasis (TRBR), and ground glass opacity (GGO). Pulmonary vessels were segmented with the automatic integration segmentation method. All segmentation results were quantified by the corresponding segmentation software. Correlations between the volume of the 4 findings on HRCT, volume of the lesions at different sites, pulmonary vascular-related parameters, and pulmonary function tests were analyzed.

RESULTS

A total of 101 IPF patients (93 males) with a median age of 63 years [interquartile range (IQR), 58 to 68 years] were included in this study. Total lesion extent demonstrated a stronger negative correlation with diffusion capacity for carbon monoxide (DLco) compared to HC, RE, and TRBR [total lesion ratio, correlation coefficient (r) =-0.67, P<0.001; HC, r=-0.45, P<0.001; RE, r=-0.41, P<0.001; TRBR, r=-0.25, P<0.05, respectively]. Correlations with lung function were similar among various lesion sites with r from -0.38 to -0.61 (P<0.001). Pulmonary artery volume (PAV) displayed a slightly increased positive association with the DLco compared to total pulmonary vascular volume (PVV); for PAV, r=0.41 and P<0.001 and for total PVV, r=0.36 and P<0.001. Additionally, total lesion extent, HC, and RE indicated a negative relationship with vascular-related parameters, and the strength of the correlations was independent of lesion site.

CONCLUSIONS

Quantitative analysis of HRCT features of IPF indicated a decline in function and an aggravation of vascular destruction with increasing lesion extent. Furthermore, a positive correlation between vascular-related parameters and pulmonary function was confirmed. This co-linearity indicated the potential of vascular-related parameters as new objective markers for evaluating the severity of IPF.

摘要

背景

高分辨率计算机断层扫描(HRCT)的定量分析越来越多地用于量化疾病的严重程度和评估预后。我们的目的是量化特发性肺纤维化(IPF)的HRCT特征,并确定它们与肺功能测试的关联。

方法

这是一项回顾性、单中心临床研究。回顾性纳入IPF患者。使用基于深度学习的方法进行肺分割。放射科医生手动分割IPF的4种表现,包括蜂窝状改变(HC)、网状影(RE)、牵拉性支气管扩张(TRBR)和磨玻璃影(GGO)。采用自动积分分割方法对肺血管进行分割。所有分割结果均由相应的分割软件进行量化。分析HRCT上4种表现的体积、不同部位病变的体积、肺血管相关参数与肺功能测试之间的相关性。

结果

本研究共纳入101例IPF患者(93例男性),中位年龄63岁[四分位间距(IQR),58至68岁]。与HC、RE和TRBR相比,总病变范围与一氧化碳弥散量(DLco)的负相关性更强[总病变比率,相关系数(r)=-0.67,P<0.001;HC,r=-0.45,P<0.001;RE,r=-0.41,P<0.001;TRBR,r=-0.25,P<0.05]。不同病变部位与肺功能的相关性相似,r为-0.38至-0.61(P<0.001)。与总肺血管容积(PVV)相比,肺动脉容积(PAV)与DLco的正相关性略有增加;PAV的r=0.41,P<0.001,总PVV的r=0.36,P<0.001。此外,总病变范围、HC和RE与血管相关参数呈负相关,且相关性强度与病变部位无关。

结论

IPF的HRCT特征定量分析表明,随着病变范围的增加,功能下降,血管破坏加重。此外,证实了血管相关参数与肺功能之间存在正相关。这种共线性表明血管相关参数作为评估IPF严重程度的新客观标志物的潜力。

相似文献

2
Quantitative CT analysis of idiopathic pulmonary fibrosis and correlation with lung function study.
BMC Pulm Med. 2024 Sep 5;24(1):437. doi: 10.1186/s12890-024-03254-9.
3
Idiopathic pulmonary fibrosis disease progression: a dynamic quantitative chest computed tomography follow-up analysis.
Quant Imaging Med Surg. 2023 Mar 1;13(3):1488-1498. doi: 10.21037/qims-22-843. Epub 2023 Jan 9.
8
Quantitative Evaluation of Fibrosis in IPF Patients: Meaning of Diffuse Pulmonary Ossification.
Diagnostics (Basel). 2021 Jan 12;11(1):113. doi: 10.3390/diagnostics11010113.

引用本文的文献

2
A systematic review of the role of quantitative CT in the prognostication and disease monitoring of interstitial lung disease.
Eur Respir Rev. 2025 Apr 30;34(176). doi: 10.1183/16000617.0194-2024. Print 2025 Apr.
5
Radiomics and Artificial Intelligence in Pulmonary Fibrosis.
J Imaging Inform Med. 2025 Jan 6. doi: 10.1007/s10278-024-01377-3.
9
Idiopathic pulmonary fibrosis disease progression: a dynamic quantitative chest computed tomography follow-up analysis.
Quant Imaging Med Surg. 2023 Mar 1;13(3):1488-1498. doi: 10.21037/qims-22-843. Epub 2023 Jan 9.

本文引用的文献

2
Quantitative CT in mortality prediction in pulmonary fibrosis with or without emphysema.
Sarcoidosis Vasc Diffuse Lung Dis. 2021;38(3):e2021024. doi: 10.36141/svdld.v38i3.11044. Epub 2021 Sep 30.
3
6
Circulating Plasma Biomarkers of Survival in Antifibrotic-Treated Patients With Idiopathic Pulmonary Fibrosis.
Chest. 2020 Oct;158(4):1526-1534. doi: 10.1016/j.chest.2020.04.066. Epub 2020 May 22.
7
Evaluation of acute pulmonary embolism and clot burden on CTPA with deep learning.
Eur Radiol. 2020 Jun;30(6):3567-3575. doi: 10.1007/s00330-020-06699-8. Epub 2020 Feb 16.
8
Automated Computed Tomography analysis in the assessment of Idiopathic Pulmonary Fibrosis severity and progression.
Eur J Radiol. 2020 Mar;124:108852. doi: 10.1016/j.ejrad.2020.108852. Epub 2020 Jan 28.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验