Evidence map›Paper›PMID 42658665›Full record

ArticleRheumatology (Oxford, England)2026

Radiomic analysis of high-resolution computed tomography predicts interstitial lung disease progression and mortality in systemic sclerosis.

Maria Iacovantuono, Nicholas Landini, Lisa Jungblut, Gesa M Sauer, Florian Käs, Rucsandra Dobrota, Sinziana Muraru, Muriel Elhai, Carina Mihai, Mike O Becker and 5 more

Abstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Maria IacovantuonoDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0009-0002-4963-0663
Nicholas LandiniDepartment of Radiological, Oncological and Pathological Sciences, "Sapienza" University of Rome, Policlinico Umberto I, Rome, Italy.ORCID 0000-0002-2928-3003
Lisa JungblutInstitute for Diagnostic and Interventional Radiology, University Hospital Zurich, University Zurich, Zurich, Switzerland.ORCID 0000-0003-2078-4730
Gesa M SauerDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0000-0002-0257-8952
Florian KäsDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0009-0008-0594-9262
Rucsandra DobrotaDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0000-0001-9819-7574
Sinziana MuraruDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0009-0004-2896-153X
Muriel ElhaiDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0000-0001-8627-5758
Carina MihaiDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0000-0002-8627-8817
Mike O BeckerDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0000-0001-9102-3088
Maria Sole ChimentiDepartment of Systems Medicine, Rheumatology, Allergology and Clinical Immunology, University of Rome Tor Vergata, Rome, Italy.ORCID 0000-0002-1343-1729
Thomas FrauenfelderInstitute for Diagnostic and Interventional Radiology, University Hospital Zurich, University Zurich, Zurich, Switzerland.ORCID 0000-0002-3295-6619
Anna-Maria Hoffmann-VoldDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0000-0001-6467-7422
Oliver DistlerDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0000-0002-0546-8310
Cosimo BruniDepartment of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.ORCID 0000-0003-2813-2083

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe automated assessment of chest high-resolution CT (HRCT) scans allows the objective quantification of interstitial lung disease (ILD)-related features. Here, we explored the ability of HRCT-derived radiomic features to predict all-cause mortality and ILD progression in SSc-ILD patients.

methodsWe analysed baseline and follow-up HRCT scans of SSc-ILD patients using lung texture analysis (LTA™, Imbio). Lung parenchymal alterations (honeycombing, ground-glass, reticulation, hyperlucency) and pulmonary vessel volume (PVV) were quantified as percentages of the respective lung volume-for whole lungs and for upper, middle and lower zones. Univariable and multivariable Cox regression and generalized estimating equation (GEE) models were applied to identify radiomics predictors of all-cause mortality and ILD progression, respectively.

resultsOf 313 SSc-ILD patients, 267 (85%) were eligible for radiomic analysis and were included in the mortality analysis; 160 (60%) were included in the progression analysis. Over 42 [interquartile range (IQ)R 27-110] months of follow-up, 65 (24%) patients died. They presented with a greater extent of PVV% and parenchymal alterations across all lung zones, compared with patients who survived. PVV% independently predicted mortality [adjusted hazard ratio (HR) 1.21, 95% CI 1.094-1.354], particularly in the upper zones (adjusted HR 1.28, 95% CI 1.11-1.46). Among 261 yearly follow-up visits from 160 SSc-ILD patients, 50.6% showed at least one episode of ILD progression, for a total of 99 (37.7%) episodes. Baseline radiomic features were overall comparable between progressors and non-progressors. The extent of whole-lung honeycombing was identified as the only independent radiomic predictor of ILD progression [adjusted odds ratio 1.53, 95% CI 1.17-2.01].

conclusionThe PVV% and the extent of honeycombing independently predict mortality and ILD progression, respectively. These radiomic features might support risk stratification of SSc-ILD patients, on top of functional and clinical characteristics.

Indexed as

LungLung Diseases, InterstitialScleroderma, SystemicTomography, X-Ray ComputedAgedDisease ProgressionFemaleHumansMaleMiddle AgedPredictive Value of TestsPrognosisRadiomicsRetrospective StudiesILD progressioninterstitial lung diseasemortalityradiomicssystemic sclerosis

Identifiers

PMID42658665
PMCPMC13592468

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.