Evidence map›Paper›PMID 16709694›Full record

ArticleHeart (British Cardiac Society)2006

Distribution of SPARC during neovascularisation of degenerative aortic stenosis.

A Charest, A Pépin, R Shetty, C Côté, P Voisine, F Dagenais, P Pibarot, P Mathieu

Registry-linked trialAbstract read
In one paragraph

Article in Heart (British Cardiac Society), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01679431 (Metabolic Determinants of the Progression of Aortic Stenosis - PROGRESSA Study), which is not on this map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
6.6field-weighted citation impact, top 3% 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.

NCT01679431 unknown statusnot on this map

Metabolic Determinants of the Progression of Aortic Stenosis - PROGRESSA Study

TypeobservationalSponsorLaval UniversityRan2005 to 2024Enrolled250ConditionsAortic Valve StenosisArmsDoppler-echocardiography, Computed tomography, Magnetic resonance imaging, Fasting blood sample
3 · Its place in the literature

Who cites it

36 citing papers in PubMed, 90 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Bioprosthetic heart valve structural degeneration associated with metabolic syndrome: Mitigation with polyoxazoline modification.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  5. Article
  6. Review
  7. Review
  8. Association Between Serum Leptin Level and Calcific Aortic Valve Disease.Journal of the American Heart Association · 2019
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Calcific aortic stenosis.Nature reviews. Disease primers · 2016
    Review
  15. Osteopontin is proteolytically processed by matrix metalloproteinase 9.Canadian journal of physiology and pharmacology · 2015
    Article
  16. Article
  17. Article
  18. Review
  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

8 authors at 2 institutions in 1 country.

A CharestLaval Hospital Research Center/Quebec Heart Institute, Department of Surgery, Laval University, Ste-Foy, Quebec, Canada.
A Pépin
R Shetty
C Côté
P Voisine
F Dagenais
P Pibarot
P Mathieu
Université Laval · CACegep de Sainte Foy · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo examine the hypothesis that degenerative aortic stenosis (AS) is associated with the development of blood vessels and the expression of the secreted protein, acidic and rich in cysteine/osteonectin (SPARC), a matricellular protein that is involved in ossification, the modulation of angiogenesis and the production of metalloproteinases.

methods30 surgically excised AS valves and 20 normal aortic valves were studied.

resultsBlood vessels were detected in the aortic valves from patients with degenerative AS, whereas normal valves were avascular structures. Blood vessels in AS valves expressed endothelial nitric oxide synthase, CD34 and von Willebrand factor (vWF). Blood vessels were located in three distinct regions: near calcified nodules, under the leaflet border and in rich cellular areas forming cell islands. Blood vessels were predominantly present in early and intermediate grades of calcification. Cell islands were densely populated by CD45-positive cells where endothelial cells (CD34+, vWF+) forming cord-like structures were present. Immunoblotting detected SPARC only in AS valves and immunohistological analysis located SPARC in mature blood vessels. The proportion of blood vessels positive for SPARC was higher in valves with a lower grade of calcification. In cell islands, SPARC was distributed to mature blood vessels and to macrophages, where it co-located with matrix metalloproteinase-9, whereas no expression was detected in endothelial cells forming cord-like structures.

conclusionThe localisation of SPARC to mature blood vessels and its predominant expression in AS valves with a lower calcification grade suggest that the spatial and temporal distribution of this matricellular protein is tightly controlled to participate in the neovascularisation of AS valves.

Indexed as

AgedAortic ValveAortic Valve StenosisBlotting, WesternCase-Control StudiesFemaleHumansImmunohistochemistryMaleMatrix Metalloproteinase 9Neovascularization, PathologicOsteonectinMatrix Metalloproteinase 9Osteonectin

Identifiers

PMID16709694
PMCPMC1861285
OpenAlexW2098107069

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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.