Evidence map›Paper›PMID 32134199›Full record

ArticleArthritis & rheumatology (Hoboken, N.J.)2020

Current and Future Outlook on Disease Modification and Defining Low Disease Activity in Systemic Sclerosis.

Vivek Nagaraja, Marco Matucci-Cerinic, Daniel E Furst, Masataka Kuwana, Yannick Allanore, Christopher P Denton, Ganesh Raghu, Vallerie Mclaughlin, Panduranga S Rao, James R Seibold and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Arthritis & rheumatology (Hoboken, N.J.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 5% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
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  13. Promise and challenge of systemic sclerosis therapies.Nature reviews. Rheumatology · 2021
    Article
  14. Observational
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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

13 authors at 9 institutions in 5 countries.

Vivek NagarajaUniversity of Michigan, Ann Arbor.ORCID 0000-0002-4930-3200
Marco Matucci-CerinicUniversity of Florence, Florence, Italy.
Daniel E FurstUniversity of California in Los Angeles, University of Washington, Seattle, and University of Florence, Florence, Italy.
Masataka KuwanaNippon Medical School, Tokyo, Japan.ORCID 0000-0001-8352-6136
Yannick AllanoreParis Descartes University, INSERM U1016, Université Sorbonne Paris Cité, and Cochin Hospital, Paris, France.
Christopher P DentonUniversity College London and Royal Free Hospital, London, UK.
Ganesh RaghuUniversity of Washington, Seattle.
Vallerie MclaughlinUniversity of Michigan, Ann Arbor.
Panduranga S RaoUniversity of Michigan, Ann Arbor.
James R SeiboldScleroderma Research Consultants, LLC, Aiken, South Carolina.
John D PaulingRoyal National Hospital for Rheumatic Diseases, Royal United Hospitals, Bath, UK.ORCID 0000-0002-2793-2364
Michael L WhitfieldGeisel School of Medicine at Dartmouth, Hanover, New Hampshire.
Dinesh KhannaUniversity of Michigan, Ann Arbor.ORCID 0000-0003-1412-4453
University of Michigan · USUniversity of Washington · USDartmouth College · USDélégation Paris 5 · FRNippon Medical School · JPRoyal National Hospital for Rheumatic Diseases · GBThe Royal Free Hospital · GBUniversity of Florence · ITUniversity of South Carolina Aiken · US

Funding

Outcomes Research in Rheumatic DiseasesK24AR063120 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KHANNA, DINESH · 2012 to 2022
$1.6M
Systemic Sclerosis-Associated Interstitial Lung Disease Response IndexR01AR070470 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI KHANNA, DINESH · 2017 to 2019
$642k
NIAMS NIH HHS K24 AR063120NIAMS NIH HHS R01 AR070470
6 · The paper itself

Abstract

Systemic sclerosis (SSc) is an autoimmune rheumatic disease with heterogeneous clinical manifestations and a variable course in which the severity of the pathology dictates the disease prognosis and course. Among autoimmune rheumatic diseases, SSc has the highest mortality rate among all rheumatic diseases, though there are exciting new therapeutic targets that appear to halt the progression of SSc manifestations such as skin or lung fibrosis. In selected patients, high-intensity regimens with autologous stem cell transplantation can favorably modify the course. In what was once thought to be an untreatable disease, targeted therapies have now changed the outlook of SSc to a treatable disorder. Herein, we discuss the targeted therapies modifying the outlook on selected organ involvement and creating opportunities for future treatment. We also present a framework for defining low disease activity in SSc.

Indexed as

Acute DiseaseAntihypertensive AgentsDisease ProgressionEndothelin Receptor AntagonistsFibrosisFingersHeart DiseasesHematopoietic Stem Cell TransplantationHumansImmunosuppressive AgentsKidney DiseasesLung Diseases, InterstitialMyocardiumOutcome Assessment, Health CareProstaglandins IPulmonary Arterial HypertensionAntihypertensive AgentsEndothelin Receptor AntagonistsImmunosuppressive AgentsProstaglandins I

Identifiers

PMID32134199
PMCPMC7329619
OpenAlexW3010510320

What OpenQuestion holds

Textmetadata
LicenceTDM
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.