4.6 Article

Quantitative computed tomography predicts outcomes in idiopathic pulmonary fibrosis

期刊

RESPIROLOGY
卷 27, 期 12, 页码 1045-1053

出版社

WILEY
DOI: 10.1111/resp.14333

关键词

data-driven texture analysis; idiopathic pulmonary fibrosis; pulmonary function; quantitative computed tomography

资金

  1. Australian IPF Registry
  2. NHMRC Centre of Research Excellence in Pulmonary Fibrosis
  3. Lung Foundation Australia
  4. Boehringer Ingelheim
  5. Roche Products Pty.
  6. Galapagos and Bristol-Myers Squibb Australia

向作者/读者索取更多资源

This study assessed the prognostic value of quantifying lung fibrosis extent using data-driven texture analysis (DTA) in a large cohort of idiopathic pulmonary fibrosis (IPF) patients. The results showed that the extent of fibrotic abnormality on baseline CT analyzed via DTA was associated with outcomes independent of pulmonary function.
Background and objectivePrediction of disease course in patients with progressive pulmonary fibrosis remains challenging. The purpose of this study was to assess the prognostic value of lung fibrosis extent quantified at computed tomography (CT) using data-driven texture analysis (DTA) in a large cohort of well-characterized patients with idiopathic pulmonary fibrosis (IPF) enrolled in a national registry. MethodsThis retrospective analysis included participants in the Australian IPF Registry with available CT between 2007 and 2016. CT scans were analysed using the DTA method to quantify the extent of lung fibrosis. Demographics, longitudinal pulmonary function and quantitative CT metrics were compared using descriptive statistics. Linear mixed models, and Cox analyses adjusted for age, gender, BMI, smoking history and treatment with anti-fibrotics were performed to assess the relationships between baseline DTA, pulmonary function metrics and outcomes. ResultsCT scans of 393 participants were analysed, 221 of which had available pulmonary function testing obtained within 90 days of CT. Linear mixed-effect modelling showed that baseline DTA score was significantly associated with annual rate of decline in forced vital capacity and diffusing capacity of carbon monoxide. In multivariable Cox proportional hazard models, greater extent of lung fibrosis was associated with poorer transplant-free survival (hazard ratio [HR] 1.20, p < 0.0001) and progression-free survival (HR 1.14, p < 0.0001). ConclusionIn a multi-centre observational registry of patients with IPF, the extent of fibrotic abnormality on baseline CT quantified using DTA is associated with outcomes independent of pulmonary function.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据