Evidence map›Paper›PMID 39775478›Full record

ArticleRheumatology (Oxford, England)2025

Gastroesophageal reflux disease is associated with a more severe interstitial lung disease in systemic sclerosis in the EUSTAR cohort.

Eliane Roth, Cosimo Bruni, Liubov Petelytska, Mike Oliver Becker, Rucsandra Dobrota, Suzana Jordan, Carina Mihai, Sinziana Muraru, Patricia E Carreira, Jeska De Vries-Bouwstra and 17 more

Abstract read
In one paragraph

Article in Rheumatology (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 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

27 authors.

Eliane RothDepartment of Rheumatology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Cosimo BruniDepartment of Rheumatology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Liubov PetelytskaDepartment of Rheumatology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Mike Oliver BeckerDepartment of Rheumatology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.ORCID 0000-0001-9102-3088
Rucsandra DobrotaDepartment of Rheumatology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Suzana JordanDepartment of Rheumatology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Carina MihaiDepartment of Rheumatology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Sinziana MuraruDepartment of Rheumatology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.
Patricia E CarreiraRheumatology Department, Hospital Universitario, 12 De Octubre, Madrid, Spain.
Jeska De Vries-BouwstraDepartment of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands.
Yolanda Braun-MoscoviciRappaport Faculty of Medicine, Rheumatology Institute Rambam Health Care Campus, Technion, Haifa, Israel.ORCID 0000-0001-7706-9346
Vasiliki LiakouliRheumatology Unit, Department of Precision Medicine, University of Campania "Luigi Vanvitelli", Naples, Italy.
Gianluca MoronciniClinica Medica, Department of Internal Medicine, Marche University Hospital, Ancona, Italy.
Christina BergmannDepartment Internal Medicine 3, University Hospital Erlangen, Erlangen, Germany.
Luc MouthonDepartment of Internal Medicine, Hôpital Cochin, Paris, France.
Christopher P DentonDivision of Medicine, Department of Inflammation and Rare Diseases, Centre For Rheumatology Royal Free Hospital and University College London, London, UK.ORCID 0000-0003-3975-8938
Maria De SantisIRCCS Humanitas Research Hospital, Rozzano, Italy.ORCID 0000-0002-3196-1336
Alberto CauliRheumatology Unit, AOU and University Hospital of Cagliari, Monserrato (CA), Italy.
Sabine AdlerDepartment of Rheumatology and Immunology, Kantonsspital Aarau, Aarau, Switzerland.
Vera BernardinoUnidade de Doenças Autoimunes-Hospital Curry Cabral, Centro Hospitalar Universitário Lisboa Central, ULS S. José, Centro Clínico Académico de Lisboa, Portugal.
Marie-Elise TruchetetDepartment of Rheumatology, Bordeaux University Hospital, Bordeaux, France.
Madelon VonkDepartment of Rheumatology, Radboud University Medical Center, Nijmegen, The Netherlands.
Francesco Del GaldoLeeds Institute of Rheumatic and Muskuloskeletal Medicine, University of Leeds, Leeds, UK.
Anna-Maria Hoffmann-VoldDepartment of Rheumatology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.ORCID 0000-0001-6467-7422
Oliver DistlerDepartment of Rheumatology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.ORCID 0000-0002-0546-8310
Muriel ElhaiDepartment of Rheumatology, University Hospital Zurich and University of Zurich, Zurich, Switzerland.ORCID 0000-0001-8627-5758
EUSTAR Collaborators

Funding

AbbVieBoehringer IngelheimFoundation for Research in RheumatologyWelcome Trust
6 · The paper itself

Abstract

objectivesGastroesophageal reflux disease (GERD) is frequent in systemic sclerosis (SSc) and could predict progression of interstitial lung disease (ILD). We aimed to analyse (1) the prevalence of GERD among SSc-ILD patients, (2) its association with disease characteristics and (3) predictive factors for ILD progression in SSc-ILD patients with GERD.

methodsSSc patients from the EUSTAR database with ILD were included. GERD was labelled as present if reflux/dysphagia was reported at the baseline visit or before. Disease characteristics of patients with and without GERD were compared at baseline. ILD progression was defined as relative FVC decline ≥10% or relative FVC decline between 5-9% in association with relative DLCO decline of ≥15% over 12 ± 3 months of follow-up. Prognostic factors for ILD progression, overall survival and progression-free survival in SSc-ILD patients with GERD were tested by multivariable Cox regression.

resultsA total of 5462 SSc-ILD patients were included, 4400 (80.6%) had GERD. Patients with GERD presented more frequently with diffuse cutaneous SSc (OR: 1.44 [1.22-1.69], P < 0.001) and more severe lung involvement with lower FVC (85.8 ± 22.1 vs 90.2 ± 20.1, P < 0.001), lower DLCO (60.8 ± 19.7 vs 65.3 ± 20.6, P < 0.001) and worse performance at the 6-min walking test. Female sex (HR: 1.39 [1.07-1.80], P = 0.012) and older age (HR: 1.02 [1.01-1.03], P < 0.001) independently predicted ILD progression in SSc-ILD patients with GERD.

conclusionSSc-ILD patients with GERD appear to suffer from a more severe SSc disease. In this population, female sex may be considered a risk factor for ILD progression.

Indexed as

Gastroesophageal RefluxLung Diseases, InterstitialScleroderma, SystemicAgedDisease ProgressionFemaleHumansMaleMiddle AgedPrevalencePrognosisRisk FactorsSeverity of Illness Indexgastroesophageal reflux diseaseinterstitial lung diseaseprogressionsystemic sclerosis

Identifiers

PMID39775478
PMCPMC12695048

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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.