Evidence map›Paper›PMID 40794200›Full record

Observational studyRheumatology international2025

The association of symptoms, pulmonary function test and computed tomography in interstitial lung disease at the onset of connective tissue disease: an observational study with artificial intelligence analysis of high-resolution computed tomography.

Tobias Hoffmann, Ulf Teichgräber, Luis Benedict Brüheim, Bianca Lassen-Schmidt, Diane Renz, Tobias Weise, Martin Krämer, Peter Oelzner, Joachim Böttcher, Felix Güttler and 2 more

Abstract readObservational Study
In one paragraph

Observational study in Rheumatology international, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Tobias HoffmannDepartment of Internal Medicine III, Center of Rheumatology, Jena University Hospital, Friedrich Schiller University Jena, Am Klinikum 1, 07747, Jena, Germany.ORCID http://orcid.org/0000-0003-2959-1126
Ulf TeichgräberInstitute of Diagnostic and Interventional Radiology, Jena University Hospital, Friedrich Schiller University Jena, Jena, Germany.ORCID http://orcid.org/0000-0002-4048-3938
Luis Benedict BrüheimDepartment of Internal Medicine III, Center of Rheumatology, Jena University Hospital, Friedrich Schiller University Jena, Am Klinikum 1, 07747, Jena, Germany.
Bianca Lassen-SchmidtFraunhofer Institute for Digital Medicine MEVIS, Bremen, Germany.ORCID http://orcid.org/0000-0001-7888-9928
Diane RenzInstitute of Diagnostic and Interventional Radiology, Department of Pediatric Radiology, Hannover Medical School, Hannover, Germany.ORCID http://orcid.org/0000-0002-3764-3697
Tobias WeiseBioControl Jena GmbH, Jena, Germany.
Martin KrämerInstitute of Diagnostic and Interventional Radiology, Jena University Hospital, Friedrich Schiller University Jena, Jena, Germany.ORCID http://orcid.org/0000-0002-0173-9830
Peter OelznerDepartment of Internal Medicine III, Center of Rheumatology, Jena University Hospital, Friedrich Schiller University Jena, Am Klinikum 1, 07747, Jena, Germany.ORCID http://orcid.org/0000-0002-2218-4096
Joachim BöttcherDepartment of Internal Medicine III, Center of Rheumatology, Jena University Hospital, Friedrich Schiller University Jena, Am Klinikum 1, 07747, Jena, Germany.
Felix GüttlerInstitute of Diagnostic and Interventional Radiology, Jena University Hospital, Friedrich Schiller University Jena, Jena, Germany.ORCID http://orcid.org/0000-0002-4414-2188
Gunter WolfDepartment of Internal Medicine III, Center of Rheumatology, Jena University Hospital, Friedrich Schiller University Jena, Am Klinikum 1, 07747, Jena, Germany.ORCID http://orcid.org/0000-0002-3291-0610
Alexander PfeilDepartment of Internal Medicine III, Center of Rheumatology, Jena University Hospital, Friedrich Schiller University Jena, Am Klinikum 1, 07747, Jena, Germany. alexander.pfeil@med.uni-jena.de.ORCID http://orcid.org/0000-0002-2709-6685

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interstitial lung disease (ILD) is a common and serious organ manifestation in patients with connective tissue disease (CTD), but it is uncertain whether there is a difference in ILD between symptomatic and asymptomatic patients. Therefore, we conducted a study to evaluate differences in the extent of ILD based on radiological findings between symptomatic/asymptomatic patients, using an artificial intelligence (AI)-based quantification of pulmonary high-resolution computed tomography (AIpqHRCT). Within the study, 67 cross-sectional HRCT datasets and clinical data (including pulmonary function test) of consecutively patients (mean age: 57.1 ± 14.7 years, woman n = 45; 67.2%) with both, initial diagnosis of CTD, with systemic sclerosis being the most frequent (n = 21, 31.3%), and ILD (all without immunosuppressive therapy), were analysed using AIqpHRCT. 25.4% (n = 17) of the patients with ILD at initial diagnosis of CTD had no pulmonary symptoms. Regarding the baseline characteristics (age, gender, disease), there were no significant difference between the symptomatic and asymptomatic group. The pulmonary function test (PFT) revealed the following mean values (%predicted) in the symptomatic and asymptomatic group, respectively: Forced vital capacity (FVC) 69.4 ± 17.4% versus 86.1 ± 15.8% (p = 0.001), and diffusing capacity of the lung for carbon monoxide (DLCO) 49.7 ± 17.9% versus 60.0 ± 15.8% (p = 0.043). AIqpHRCT data showed a significant higher amount of high attenuated volume (HAV) (14.8 ± 11.0% versus 8.9 ± 3.9%; p = 0.021) and reticulations (5.4 ± 8.7% versus 1.4 ± 1.5%; p = 0.035) in symptomatic patients. A quarter of patients with ILD at the time of initial CTD diagnosis had no pulmonary symptoms, showing DLCO were reduced in both groups. Also, AIqpHRCT demonstrated clinically relevant ILD in asymptomatic patients. These results underline the importance of an early risk adapted screening for ILD also in asymptomatic CTD patients, as ILD is associated with increased mortality.

Indexed as

Artificial IntelligenceConnective Tissue DiseasesLungLung Diseases, InterstitialTomography, X-Ray ComputedAdultAgedCross-Sectional StudiesFemaleHumansMaleMiddle AgedRespiratory Function TestsAI-based quantification of pulmonary HRCTArtificial intelligenceConnective tissue diseasesHRCTInflammatory rheumatic diseasesInterstitialInterstitial lung diseaseLung diseasesPulmonary symptomsQuantificationRheumatic diseasesTomographyX-ray computed

Identifiers

PMID40794200
PMCPMC12343718

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Registered trials

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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 OpenQuestion graph.