Evidence map›Paper›PMID 36849541›Full record

ReviewNature reviews. Rheumatology2023

State-of-the-art evidence in the treatment of systemic sclerosis.

Janet E Pope, Christopher P Denton, Sindhu R Johnson, Andreu Fernandez-Codina, Marie Hudson, Tatiana Nevskaya

Open access · bronzeAbstract readReview
In one paragraph

Review in Nature reviews. Rheumatology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 111 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
111citing papers in PubMed, 5 pooled it
45.1field-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

111 citing papers in PubMed, 5 syntheses or guidelines pooled it, 177 citations in OpenAlex.

  1. Pooled it
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  6. Review
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  18. Automatic assessment of lung involvement in systemic sclerosis using deep learning.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2026
    Article
  19. Review
  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 6 institutions in 3 countries.

Janet E PopeDivision of Rheumatology, St Joseph's Health Care, London, ON, Canada. janet.pope@sjhc.london.on.ca.ORCID http://orcid.org/0000-0003-1479-5302
Christopher P DentonDivision of Medicine, University College London, London, UK.ORCID http://orcid.org/0000-0003-3975-8938
Sindhu R JohnsonToronto Scleroderma Program, Toronto Western Hospital, Mount Sinai Hospital, Toronto, ON, Canada.ORCID http://orcid.org/0000-0003-0591-2976
Andreu Fernandez-CodinaDivision of Rheumatology, St Joseph's Health Care, London, ON, Canada.
Marie HudsonDepartment of Medicine, McGill University, Montreal, QC, Canada.
Tatiana NevskayaDivision of Rheumatology, St Joseph's Health Care, London, ON, Canada.
Jewish General Hospital · CAMount Sinai Hospital · CASt Joseph's Health Care · CAUniversity College London · GBWestern University · CAWindsor Regional Hospital · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic sclerosis (SSc) is a rare autoimmune connective tissue disease with multi-organ involvement, fibrosis and vasculopathy. Treatment in SSc, including early diffuse cutaneous SSc (dcSSc) and the use of organ-specific therapies, has improved, as evident from randomized clinical trials. Treatments for early dcSSc include immunosuppressive agents such as mycophenolate mofetil, methotrexate, cyclophosphamide, rituximab and tocilizumab. Patients with rapidly progressive early dcSSc might be eligible for autologous haematopoietic stem cell transplantation, which can improve survival. Morbidity from interstitial lung disease and pulmonary arterial hypertension is improving with the use of proven therapies. Mycophenolate mofetil has surpassed cyclophosphamide as the initial treatment for SSc-interstitial lung disease. Nintedanib and possibly perfinidone can be considered in SSc pulmonary fibrosis. Pulmonary arterial hypertension is frequently treated with initial combination therapy (for example, with phosphodiesterase 5 inhibitors and endothelin receptor antagonists) and, if necessary, the addition of a prostacyclin analogue. Raynaud phenomenon and digital ulcers are treated with dihydropyridine calcium channel blockers (especially nifedipine), then phosphodiesterase 5 inhibitors or intravenous iloprost. Bosentan can reduce the development of new digital ulcers. Trial data for other manifestations are mostly lacking. Research is needed to develop targeted and highly effective treatments, best practices for organ-specific screening and early intervention, and sensitive outcome measurements.

Indexed as

Lung Diseases, InterstitialPulmonary Arterial HypertensionScleroderma, SystemicCyclophosphamideHumansMycophenolic AcidPhosphodiesterase 5 InhibitorsSkin UlcerCyclophosphamideMycophenolic AcidPhosphodiesterase 5 Inhibitors

Identifiers

PMID36849541
PMCPMC9970138
OpenAlexW4322418740

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.