Evidence map›Paper›PMID 32079645›Full record

ReviewThe European respiratory journal2020

Predictors of progression in systemic sclerosis patients with interstitial lung disease.

Oliver Distler, Shervin Assassi, Vincent Cottin, Maurizio Cutolo, Sonye K Danoff, Christopher P Denton, Jörg H W Distler, Anna-Maria Hoffmann-Vold, Sindhu R Johnson, Ulf Müller Ladner and 3 more

Open access · bronzeAbstract readReview
In one paragraph

Review in The European respiratory journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed, 1 pooled it
20.3field-weighted citation impact, top 1% of its field
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

117 citing papers in PubMed, 1 synthesis or guideline pooled it, 232 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Prevalence and Prognostic Impact of Progressive Pulmonary Fibrosis.Tuberculosis and respiratory diseases · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article

57 more citing papers are in PubMed but not listed here.

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

13 authors at 12 institutions in 9 countries.

Oliver DistlerDept of Rheumatology, University Hospital Zurich, Zurich, Switzerland.
Shervin AssassiDept of Rheumatology and Clinical Immunogenetics, McGovern Medical School, University of Texas, Houston, TX, USA.
Vincent CottinNational Reference Center for Rare Pulmonary Diseases, Louis Pradel Hospital, Hospices Civils de Lyon, Claude Bernard University Lyon 1, UMR754, Lyon, France.ORCID 0000-0002-5591-0955
Maurizio CutoloResearch Laboratory, Clinical Division of Rheumatology, Dept of Internal Medicine DIMI, University of Genoa, IRCSS Polyclinic Hospital San Martino, Genoa, Italy.
Sonye K DanoffDivision of Pulmonary and Critical Care Medicine, Johns Hopkins Medicine, Baltimore, MD, USA.
Christopher P DentonUCL Centre for Rheumatology and Connective Tissue Diseases, Royal Free Hospital, London, UK.ORCID 0000-0003-3975-8938
Jörg H W DistlerDept of Internal Medicine 3, University of Erlangen-Nuremberg, Erlangen, Germany oliver.distler@usz.ch.
Anna-Maria Hoffmann-VoldDept of Rheumatology, Oslo University Hospital, Oslo, Norway.
Sindhu R JohnsonToronto Scleroderma Program, Dept of Medicine, Toronto Western and Mount Sinai Hospitals, University of Toronto, Toronto, ON, Canada.
Ulf Müller LadnerDept of Rheumatology and Clinical Immunology, Justus-Liebig University Giessen, Campus Kerckhoff, Bad Nauheim, Germany.
Vanessa SmithDept of Rheumatology, Ghent University Hospital, Ghent, Belgium.ORCID 0000-0001-6271-7945
Elizabeth R VolkmannDept of Medicine, Division of Rheumatology, University of California, David Geffen School of Medicine, Los Angeles, CA, USA.
Toby M MaherNational Heart and Lung Institute, Imperial College London, London, UK.
Friedrich-Alexander-Universität Erlangen-Nürnberg · DEGhent University Hospital · BEJohns Hopkins University · USJustus-Liebig-Universität Gießen · DEMount Sinai Hospital · CAOslo University Hospital · NOOspedale Policlinico San Martino · ITRoyal Brompton Hospital · GBThe Royal Free Hospital · GBUniversité Claude Bernard Lyon 1 · FRUniversity Hospital of Zurich · CHUniversity of California, Los Angeles · US

Funding

HSRD VA CDA 13-017
6 · The paper itself

Abstract

Systemic sclerosis (SSc) is a systemic autoimmune disease affecting multiple organ systems, including the lungs. Interstitial lung disease (ILD) is the leading cause of death in SSc.There are no valid biomarkers to predict the occurrence of SSc-ILD, although auto-antibodies against anti-topoisomerase I and several inflammatory markers are candidate biomarkers that need further evaluation. Chest auscultation, presence of shortness of breath and pulmonary function testing are important diagnostic tools, but lack sensitivity to detect early ILD. Baseline screening with high-resolution computed tomography (HRCT) is therefore necessary to confirm an SSc-ILD diagnosis. Once diagnosed with SSc-ILD, patients' clinical courses are variable and difficult to predict, although certain patient characteristics and biomarkers are associated with disease progression. It is important to monitor patients with SSc-ILD for signs of disease progression, although there is no consensus about which diagnostic tools to use or how often monitoring should occur. In this article, we review methods used to define and predict disease progression in SSc-ILD.There is no valid definition of SSc-ILD disease progression, but we suggest that either a decline in forced vital capacity (FVC) from baseline of ≥10%, or a decline in FVC of 5-9% in association with a decline in diffusing capacity of the lung for carbon monoxide of ≥15% represents progression. An increase in the radiographic extent of ILD on HRCT imaging would also signify progression. A time period of 1-2 years is generally used for this definition, but a decline over a longer time period may also reflect clinically relevant disease progression.

Indexed as

Disease ProgressionTomography, X-Ray ComputedBiomarkersCarbon MonoxideHumansLungLung Diseases, InterstitialRespiratory Function TestsScleroderma, SystemicBiomarkersCarbon Monoxide

Identifiers

PMID32079645
PMCPMC7236865
OpenAlexW3007003780

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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 OpenQuestion graph.