Evidence map›Paper›PMID 19296882›Full record

ReviewCurrent rheumatology reports2009

Is scleroderma a vasculopathy?

Jo Nadine Fleming, Richard A Nash, William M Mahoney, Stephen Mark Schwartz

Open access · greenAbstract readReview
In one paragraph

Review in Current rheumatology reports, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.2field-weighted citation impact, top 14% 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

28 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Observational
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Cardiovascular disease in systemic sclerosis.Annals of translational medicine · 2015
    Review
  15. Article
  16. Article
  17. Animal models of systemic sclerosis: their utility and limitations.Open access rheumatology : research and reviews · 2014
    Review
  18. Article
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Jo Nadine FlemingUniversity of Washington School of Medicine, 815 Mercer Street, #419, Brotman Building, Seattle, WA 98109, USA. flemij@u.washington.edu
Richard A Nash
William M Mahoney
Stephen Mark Schwartz
University of Washington · US

Funding

Vasular cell origins and fates in granulation tissueP01HL003174 · NHLBI · UNIVERSITY OF WASHINGTON · PI SCHWARTZ, EMILY J. · 1985 to 2007
$13.8M
NHLBI NIH HHS P01 HL003174
6 · The paper itself

Abstract

Described as an autoimmune collagen vascular disease, the most striking feature of scleroderma may be a systemic vasculopathy. This vasculopathy includes characteristic noninflammatory macrovascular and microvascular changes with dramatic and possibly occlusive formation of a thickened neointima. Scleroderma vessels also have an unusual endothelial phenotype, with loss of normal markers including vascular endothelial (VE)-cadherin. These endothelial cells express type 1 interferon and regulator of G protein signaling 5 (RGS5), two molecules associated with vascular rarefaction. These genes may be important because tissue is hypoxic with high levels of vascular endothelial growth factor (VEGF), especially early in the disease. The combination of VEGF and rarefaction is not necessarily paradoxical. VEGF-mediated angiogenesis creates labile vessels that may not survive unless the vessel acquires a smooth muscle coat. The combination of interferon and RGS5 is consistent with an antiangiogenic phenotype. We offer a hypothesis that places vascular injury at the center of this disease and also suggest possible clinical approaches for arresting and/or reversing the disease.

Indexed as

AnimalsBiomarkersDisease Models, AnimalEndothelium, VascularHumansScleroderma, DiffuseScleroderma, LimitedSkinVascular DiseasesBiomarkers

Identifiers

PMID19296882
PMCPMC4091992
OpenAlexW2020978512

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.