Evidence map›Paper›PMID 35038187›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2022

Sclerostin Protects Against Vascular Calcification Development in Mice.

Annelies De Maré, Britt Opdebeeck, Ellen Neven, Patrick C D'Haese, Anja Verhulst

Open access · hybridAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed, 1 pooled it
3.8field-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

47 citing papers in PubMed, 1 synthesis or guideline pooled it, 62 citations in OpenAlex.

  1. Pooled it
  2. Bone reports · 2026
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  8. Review
  9. Article
  10. Article
  11. Article
  12. Reply.Arthritis & rheumatology (Hoboken, N.J.) · 2025
    Article
  13. Role of Sclerostin in Cardiovascular System.International journal of molecular sciences · 2025
    Review
  14. Lipopolysaccharide (LPS) induces sclerostin secretion by extracellular vesicle via TLR4/miR-92a-3p/PTEN/NF-κB signalling pathway in murine macrophage.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Article
  15. Article
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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

5 authors at 1 institution in 1 country.

Annelies De MaréLaboratory of Pathophysiology, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.ORCID 0000-0003-0063-1227
Britt OpdebeeckLaboratory of Pathophysiology, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.ORCID 0000-0002-9379-2718
Ellen NevenLaboratory of Pathophysiology, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.
Patrick C D'HaeseLaboratory of Pathophysiology, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.
Anja VerhulstLaboratory of Pathophysiology, Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium.
University of Antwerp · BE

Funding

Fonds Wetenschappelijk Onderzoek 1182417NResearch Foundation Flanders 1182419N
6 · The paper itself

Abstract

Sclerostin is a negative regulator of the Wnt/β-catenin signaling and is, therefore, an important inhibitor of bone formation and turnover. Because ectopic vascular calcification develops in a similar way to bone formation, one might reasonably attribute a role to sclerostin in this pathological process. Ectopic calcification, especially vascular calcification, importantly contributes to mortality in elderly and patients with diabetes, osteoporosis, chronic kidney disease (CKD), and hypertension. The central players in this ectopic calcification process are the vascular smooth muscle cells that undergo dedifferentiation and thereby acquire characteristics of bonelike cells. Therefore, we hypothesize that depletion/deactivation of the Wnt/β-catenin signaling inhibitor sclerostin may promote the development of ectopic calcifications through stimulation of bone-anabolic effects at the level of the arteries. We investigated the role of sclerostin (encoded by the Sost gene) during vascular calcification by using either Sost

Indexed as

Renal Insufficiency, ChronicVascular CalcificationAdaptor Proteins, Signal TransducingAdenineAgedAnimalsbeta CateninCalciumFemaleHumansMaleMiceMice, Inbred C57BLMice, Inbred DBAWarfarinAdaptor Proteins, Signal TransducingAdeninebeta CateninCalciumWarfarinBONE HISTOMORPHOMETRYMATRIX MINERALIZATIONSYSTEMS BIOLOGY - BONE INTERACTORSWnt/BETA-CATENIN

Identifiers

PMID35038187
PMCPMC9303214
OpenAlexW4206286703

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.