Evidence map›Paper›PMID 32736145›Full record

ReviewBone2020

The role of bone morphogenetic protein signaling in vascular calcification.

Peiran Yang, Luca Troncone, Zachary M Augur, Stephanie S J Kim, Megan E McNeil, Paul B Yu

Open access · greenAbstract readReview
In one paragraph

Review in Bone, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
9.5field-weighted citation impact, top 1% 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

73 citing papers in PubMed, 119 citations in OpenAlex.

  1. Article
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  12. Paeonol fromFood science and biotechnology · 2025
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13 more citing papers are in PubMed but not listed here.

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

6 authors at 2 institutions in 1 country.

Peiran YangDivision of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Luca TronconeDivision of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Zachary M AugurDivision of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Stephanie S J KimDivision of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Megan E McNeilDivision of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Paul B YuDivision of Cardiovascular Medicine, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA 02115, USA. Electronic address: pbyu@bwh.harvard.edu.
Brigham and Women's Hospital · USHarvard University · US

Funding

Novel probes of BMP and TGF-beta signaling and functionR01AR057374 · NIAMS · MASSACHUSETTS GENERAL HOSPITAL · PI YU, PAUL B · 2010 to 2023
$4.5M
HLS- Cyclic CAR peptide: a targeted therapy for pulmonary hypertensionR42HL132742 · NHLBI · VASCULAR BIOSCIENCES · PI YU, PAUL B · 2017 to 2019
$2.3M
Molecular imaging of angiogenic activity in pulmonary arterial hypertensionR01HL131910 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI YU, PAUL B · 2016 to 2018
$2.3M
Repositioning AZD0530 for surgical treatment of fibrodysplasia ossificans progressivaUG3TR002617 · NCATS · BRIGHAM AND WOMEN'S HOSPITAL · PI YU, PAUL B · 2018 to 2019
$702k
NCATS NIH HHS UG3 TR002617NHLBI NIH HHS R01 HL131910NHLBI NIH HHS R42 HL132742NIAMS NIH HHS R01 AR057374
6 · The paper itself

Abstract

Vascular calcification is associated with atherosclerosis, chronic kidney disease, and diabetes, and results from processes resembling endochondral or intramembranous ossification, or from processes that are distinct from ossification. Bone morphogenetic proteins (BMP), as well as other ligands, receptors, and regulators of the transforming growth factor beta (TGFβ) family regulate vascular and valvular calcification by modulating the phenotypic plasticity of multipotent progenitor lineages associated with the vasculature or valves. While osteogenic ligands BMP2 and BMP4 appear to be both markers and drivers of vascular calcification, particularly in atherosclerosis, BMP7 may serve to protect against calcification in chronic kidney disease. BMP signaling regulators such as matrix Gla protein and BMP-binding endothelial regulator protein (BMPER) play protective roles in vascular calcification. The effects of BMP signaling molecules in vascular calcification are context-dependent, tissue-dependent, and cell-type specific. Here we review the current knowledge on mechanisms by which BMP signaling regulates vascular calcification and the potential therapeutic implications.

Indexed as

Bone Morphogenetic ProteinsSignal TransductionVascular CalcificationBone Morphogenetic Protein 2Bone Morphogenetic Protein 4Bone Morphogenetic Protein 7Carrier ProteinsHumansBMPER protein, humanBone Morphogenetic Protein 2Bone Morphogenetic Protein 4Bone Morphogenetic Protein 7Bone Morphogenetic ProteinsCarrier ProteinsAtherosclerosisBone morphogenetic proteinChronic kidney diseaseDiabetesMedial calcificationMineralizationTransforming growth factor betaVascular calcificationVascular disease

Identifiers

PMID32736145
PMCPMC8185454
OpenAlexW3045569242

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.