Literature DB >> 35782232

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

Haishuang Sun1,2,3, Min Liu4, Han Kang5, Xiaoyan Yang2, Peiyao Zhang4, Rongguo Zhang5, Huaping Dai2,3, Chen Wang1,2,3.   

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. 2022 Quantitative Imaging in Medicine and Surgery. All rights reserved.

Entities:  

Keywords:  Idiopathic pulmonary fibrosis (IPF); high-resolution computed tomography (HRCT); pulmonary vessel; quantitative analysis

Year:  2022        PMID: 35782232      PMCID: PMC9246749          DOI: 10.21037/qims-21-1232

Source DB:  PubMed          Journal:  Quant Imaging Med Surg        ISSN: 2223-4306


  32 in total

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2.  Intraindividual variability in serial measurements of DLCO and alveolar volume over one year in eight healthy subjects using three independent measuring systems.

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3.  Quantitative CT analysis of honeycombing area in idiopathic pulmonary fibrosis: Correlations with pulmonary function tests.

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Journal:  Eur J Radiol       Date:  2015-11-07       Impact factor: 3.528

4.  Risk stratification of acute pulmonary embolism based on the clot volume and right ventricular dysfunction on CT pulmonary angiography.

Authors:  Cong Shen; Nan Yu; Leitao Wen; Sheng Zhou; Fuwen Dong; Min Liu; Youmin Guo
Journal:  Clin Respir J       Date:  2019-09-04       Impact factor: 2.570

5.  Novel Artificial Intelligence-based Technology for Chest Computed Tomography Analysis of Idiopathic Pulmonary Fibrosis.

Authors:  Tomohiro Handa; Kiminobu Tanizawa; Tsuyoshi Oguma; Ryuji Uozumi; Kizuku Watanabe; Naoya Tanabe; Takafumi Niwamoto; Hiroshi Shima; Ryobu Mori; Tomomi W Nobashi; Ryo Sakamoto; Takeshi Kubo; Atsuko Kurosaki; Kazuma Kishi; Yuji Nakamoto; Toyohiro Hirai
Journal:  Ann Am Thorac Soc       Date:  2022-03

6.  Assessment of survival in patients with idiopathic pulmonary fibrosis using quantitative HRCT indexes.

Authors:  Sebastiano Emanuele Torrisi; Stefano Palmucci; Alessandro Stefano; Giorgio Russo; Alfredo Gaetano Torcitto; Daniele Falsaperla; Mauro Gioè; Mauro Pavone; Ada Vancheri; Gianluca Sambataro; Domenico Sambataro; Letizia Antonella Mauro; Emanuele Grassedonio; Antonio Basile; Carlo Vancheri
Journal:  Multidiscip Respir Med       Date:  2018-12-01

7.  Quantitative CT analysis of honeycombing area predicts mortality in idiopathic pulmonary fibrosis with definite usual interstitial pneumonia pattern: A retrospective cohort study.

Authors:  Hiroaki Nakagawa; Emiko Ogawa; Kentaro Fukunaga; Daisuke Kinose; Masafumi Yamaguchi; Taishi Nagao; Sachiko Tanaka-Mizuno; Yasutaka Nakano
Journal:  PLoS One       Date:  2019-03-21       Impact factor: 3.240

8.  Quantitative CT in mortality prediction in pulmonary fibrosis with or without emphysema.

Authors:  Fatma Üçsular; Gülistan Karadeniz; Gülru Polat; Enver Yalnız; Aysu Ayrancı; Akin Çinkooğlu; Recep Savaş; Hatice Solmaz; Filiz Güldaval; Melih Büyükşirin
Journal:  Sarcoidosis Vasc Diffuse Lung Dis       Date:  2021-09-30       Impact factor: 0.670

9.  Prediction of idiopathic pulmonary fibrosis progression using early quantitative changes on CT imaging for a short term of clinical 18-24-month follow-ups.

Authors:  Grace Hyun J Kim; Stephan S Weigt; John A Belperio; Matthew S Brown; Yu Shi; Joshua H Lai; Jonathan G Goldin
Journal:  Eur Radiol       Date:  2019-08-26       Impact factor: 5.315

10.  Automated computed tomography quantification of fibrosis predicts prognosis in combined pulmonary fibrosis and emphysema in a real-world setting: a single-centre, retrospective study.

Authors:  Masahiro Nemoto; Yuichiro Nei; Brian Bartholmai; Kazuki Yoshida; Hiroki Matsui; Tamao Nakashita; Shinji Motojima; Masahiro Aoshima; Jay H Ryu
Journal:  Respir Res       Date:  2020-10-20
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