Evidence map›Paper›PMID 26577237›Full record

ReviewSeminars in immunopathology2016

Systemic sclerosis and localized scleroderma--current concepts and novel targets for therapy.

Oliver Distler, Antonio Cozzio

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Seminars in immunopathology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04179292 (The Effect of Physiotherapy Program in Scleroderma Patients), which is not on this map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing 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.

NCT04179292 nacompletednot on this mapstarted 2019, after this paper: background citation

The Effect of Physiotherapy Program in Scleroderma Patients: A Randomized Clinical Trial

TypeinterventionalSponsorIstanbul UniversityRan2019 to 2021Enrolled40ConditionsScleroderma, Systemic Sclerosis, Hand Rheumatism, PhysiotherapyArmsHand Therapy by Physiotherapist, Hand Therapy as home program
3 · Its place in the literature

Who cites it

38 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Erasmus syndrome: case description of a rare entity.Quantitative imaging in medicine and surgery · 2024
    Article
  6. Article
  7. Article
  8. Article
  9. Loss of Protein Kinase D2 Activity Protects Against Bleomycin-Induced Dermal Fibrosis in Mice.Laboratory investigation; a journal of technical methods and pathology · 2023
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Observational
  17. Article
  18. Article
  19. Article
  20. Review
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

2 authors.

Oliver DistlerDivision of Rheumatology, University Hospital Zurich, Gloriastr. 25, 8091, Zurich, Switzerland. oliver.distler@usz.ch.
Antonio CozzioDivision of Dermatology, University Hospital Zurich, Zurich, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Systemic sclerosis (SSc) is a chronic autoimmune disease with a high morbidity and mortality. Skin and organ fibrosis are key manifestations of SSc, for which no generally accepted therapy is available. Thus, there is a high unmet need for novel anti-fibrotic therapeutic strategies in SSc. At the same time, important progress has been made in the identification and characterization of potential molecular targets in fibrotic diseases over the recent years. In this review, we have selected four targeted therapies, which are tested in clinical trials in SSc, for in depths discussion of their preclinical characterization. Soluble guanylate cyclase (sGC) stimulators such as riociguat might target both vascular remodeling and tissue fibrosis. Blockade of interleukin-6 might be particularly promising for early inflammatory stages of SSc. Inhibition of serotonin receptor 2b signaling links platelet activation to tissue fibrosis. Targeting simultaneously multiple key molecules with the multityrosine kinase-inhibitor nintedanib might be a promising approach in complex fibrotic diseases such as SSc, in which many partially independent pathways are activated. Herein, we also give a state of the art overview of the current classification, clinical presentation, diagnostic approach, and treatment options of localized scleroderma. Finally, we discuss whether the novel targeted therapies currently tested in SSc could be used for localized scleroderma.

Indexed as

Molecular Targeted TherapyGuanylate CyclaseHumansInterleukin-6Protein Kinase InhibitorsScleroderma, LocalizedScleroderma, SystemicSerotonin AntagonistsGuanylate CyclaseInterleukin-6Protein Kinase InhibitorsSerotonin AntagonistsInterleukin-6Localized sclerodermaNintedanibSerotoninSoluble guanylate cyclaseSystemic sclerosis

Identifiers

What OpenQuestion holds

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Registered trials

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.