Evidence map›Paper›PMID 25191993›Full record

ReviewCurrent opinion in rheumatology2014

Update on scleroderma-associated interstitial lung disease.

Ming-Hui Fan, Carol A Feghali-Bostwick, Richard M Silver

Open access · greenAbstract readReview
In one paragraph

Review in Current opinion in rheumatology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Phenotypic Characterization of Transgenic Mice Expressing Human IGFBP-5.International journal of molecular sciences · 2020
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Management of Systemic-Sclerosis-Associated Interstitial Lung Disease.Rheumatic diseases clinics of North America · 2015
    Review
  11. Article
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

3 authors at 2 institutions in 1 country.

Ming-Hui FanaDivision of Pulmonary, Allergy and Critical Care Medicine, University of Pittsburgh, Pittsburgh bDivision of Rheumatology & Immunology, Medical University of South Carolina, Charleston, South Carolina, USA.
Carol A Feghali-Bostwick
Richard M Silver
Medical University of South Carolina · USUniversity of Pittsburgh · US

Funding

MOCSLID-DCCR01HL089901 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ELASHOFF, ROBERT M · 2008 to 2012
$9.1M
Patient Resource CoreP60AR062755 · NIAMS · MEDICAL UNIVERSITY OF SOUTH CAROLINA · PI GILKESON, GARY S · 2012 to 2016
$5.8M
Rheumatic Diseases Research Core CentersP30AR061271 · NIAMS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI BHAWAN, JAG · 2011 to 2015
$3.1M
Mediators of Fibrosis in Scleroderma Skin and LungR01AR050840 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FEGHALI-BOSTWICK, CAROL A. · 2003 to 2012
$3.0M
Scleroderma Twin Study and analysis of Estrogen in patients with dcSScK24AR060297 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FEGHALI-BOSTWICK, CAROL A. · 2013 to 2025
$1.4M
A Protective Role for Fibroblast Activation Protein (FAP) in Pulmonary FibrosisK08HL102266 · NHLBI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FAN, MING-HUI · 2010 to 2014
$658k
TWINS WITH SYSTEMIC SCLEROSISF32AR008373 · NIAMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI FEGHALI-BOSTWICK, CAROL A · 1996 to 1998
–
NHLBI NIH HHS 5R01HL089901NHLBI NIH HHS K08 HL102266NHLBI NIH HHS K08HL102266NIAMS NIH HHS F32 AR008373NIAMS NIH HHS K24 AR060297NIAMS NIH HHS P30 AR061271NIAMS NIH HHS P60 AR062755NIAMS NIH HHS R01 AR050840
6 · The paper itself

Abstract

purpose of reviewSystemic sclerosis (SSc), or scleroderma, is a heterogeneous and complex autoimmune disease characterized by varying degrees of skin and organ fibrosis and obliterative vasculopathy. The disease results in significant morbidity and mortality, and to date, available treatments are limited. Lung involvement is the leading cause of death of patients with SSc. Over the past year, significant advances have been made in our understanding of SSc-associated lung disease, and this review attempts to encapsulate these most recent findings and place them in context. RECENT

findingsWe divide our discussion of the most recent literature into the following: first, clinical aspects of SSc lung management, including classification, imaging, biomarkers, and treatment; second, promising new animal models that may improve our ability to accurately study this disease; and third, studies that advance or change our understanding of SSc lung disease pathogenesis, thereby raising the potential for new targets for therapeutic intervention. SUMMARY: Recent advances have resulted in a better understanding of SSc-associated lung disease, the development of new in-vivo models for exploring disease pathogenesis, and the identification of potential novel targets for the development of therapies.

Indexed as

AnimalsDisease Models, AnimalHumansLung Diseases, InterstitialScleroderma, Systemic

Identifiers

PMID25191993
PMCPMC4591932
OpenAlexW1974437007

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.