Evidence map›Paper›PMID 42583063›Full record

ArticleJournal of thoracic disease2026

Correlations between quantitative computed tomography metrics with serum fibrosis biomarkers, pulmonary function, and mortality risk in patients with idiopathic pulmonary fibrosis: a prospective cohort study.

Chenxi Yan, Yaqian Li, Minjie Mao, Zirong Wang, Yi Shen, Xueyuan Chen

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Article in Journal of thoracic disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Chenxi YanTuberculosis Intensive Care Unit, Hangzhou Red Cross Hospital, Hangzhou, China.
Yaqian LiDepartment of Respiratory Medicine, Affiliated Hospital of Hangzhou Normal University, Hangzhou, China.
Minjie MaoTuberculosis Intensive Care Unit, Hangzhou Red Cross Hospital, Hangzhou, China.
Zirong WangDepartment of Radiology, Affiliated Hospital of Hangzhou Normal University, Hangzhou, China.
Yi ShenDepartment of Respiratory Medicine, Affiliated Hospital of Hangzhou Normal University, Hangzhou, China.
Xueyuan ChenDepartment of Respiratory Medicine, Affiliated Hospital of Hangzhou Normal University, Hangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: In patients with idiopathic pulmonary fibrosis (IPF), accurate assessment of pulmonary function is critical for evaluating disease severity and predicting prognosis. We aimed to investigate correlations among quantitative computed tomography (CT) metrics, serum fibrosis biomarkers, and pulmonary function tests, as well as examining the association between quantitative imaging metrics and patient mortality. Methods: A prospective cohort study was conducted between June 2018 and December 2022. Eligible patients with IPF and healthy adults underwent quantitative CT scanning. In addition, patients underwent serum fibrosis biomarker testing and pulmonary function testing and were followed up for 2 years to record mortality. Results: A total of 57 patients and 30 healthy adults were included in the study. Sex distribution, age, body mass index, and smoking history were comparable between patients and healthy adults; however, patients showed a statistically significant higher percentage of high-attenuation area and mean image value but a lower total lung volume than healthy adults. Among patients, quantitative imaging measurements were significantly correlated with serum fibrosis biomarkers (hyaluronic acid, type IV collagen, laminin, and type III procollagen N-terminal peptide) and pulmonary function test results (forced vital capacity, forced expiratory volume in one second, and carbon monoxide diffusing capacity). During the 2-year follow-up period, 25 (43.9%) patients died. Cox proportional hazards regression analysis showed that age and quantitative imaging metrics were associated with patient mortality. Conclusions: Quantitative CT imaging can be used to assess disease severity, activity, and mortality risk in patients with IPF.

Indexed as

idiopathic pulmonary fibrosis (IPF)mortalitypulmonary functionQuantitative computed tomographyserum biomarker

Identifiers

PMID42583063
PMCPMC13459849

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.