Evidence map›Paper›PMID 34532615›Full record

ArticleJBMR plus2021

Inhibition of TGF-β Increases Bone Volume and Strength in a Mouse Model of Osteogenesis Imperfecta.

Benjamin Greene, Ryan J Russo, Shannon Dwyer, Katie Malley, Errin Roberts, Joseph Serrielo, Peter Piepenhagen, Sheila Cummings, Susan Ryan, Christine Zarazinski and 7 more

Open access · goldAbstract read
In one paragraph

Article in JBMR plus, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Osteogenesis imperfecta: pathogenesis, classification, and treatment.Clinical pediatric endocrinology : case reports and clinical investigations : official journal of the Japanese Society for Pediatric Endocrinology · 2025
    Review
  6. Anti-transforming growth factor-β treatment shows increased bone mass and strength in a novel mouse model for osteogenesis imperfecta type I.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2025
    Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. RNA-based bone histomorphometry: method and its application to explaining postpubertal bone gain in a G610C mouse model of osteogenesis imperfecta.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2024
    Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Targeting TGF-β for treatment of osteogenesis imperfecta.The Journal of clinical investigation · 2022
    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

17 authors at 3 institutions in 3 countries.

Benjamin GreeneRare and Neurologic Diseases Research Sanofi Framingham MA USA.
Ryan J RussoRare and Neurologic Diseases Research Sanofi Framingham MA USA.
Shannon DwyerRare and Neurologic Diseases Research Sanofi Framingham MA USA.
Katie MalleyGlobal Discovery Pathology Sanofi Framingham MA USA.
Errin RobertsGlobal Discovery Pathology Sanofi Framingham MA USA.
Joseph SerrieloRare and Neurologic Diseases Research Sanofi Framingham MA USA.
Peter PiepenhagenGlobal Discovery Pathology Sanofi Framingham MA USA.
Sheila CummingsGlobal Discovery Pathology Sanofi Framingham MA USA.
Susan RyanGlobal Discovery Pathology Sanofi Framingham MA USA.
Christine ZarazinskiRare and Neurologic Diseases Research Sanofi Framingham MA USA.
Sasidhar UppugantiDepartment of Orthopaedic Surgery Vanderbilt University Medical Center Nashville TN USA.
Nikolai BukanovRare and Neurologic Diseases Research Sanofi Framingham MA USA.
Jeffry S NymanDepartment of Orthopaedic Surgery Vanderbilt University Medical Center Nashville TN USA.ORCID https://orcid.org/0000-0001-7403-7605
Megan K CoxRare and Neurologic Diseases Research Sanofi Framingham MA USA.
Shiguang LiuRare and Neurologic Diseases Research Sanofi Framingham MA USA.
Oxana Ibraghimov-BeskrovnayaRare and Neurologic Diseases Research Sanofi Framingham MA USA.
Yves SabbaghRare and Neurologic Diseases Research Sanofi Framingham MA USA.ORCID https://orcid.org/0000-0001-5339-6705
Sanofi (France) · FRVanderbilt University Medical Center · USNovozymes (Denmark) · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteogenesis imperfecta (OI), is a genetic disorder of bone fragility caused by mutations in collagen I or proteins involved in collagen processing. Previous studies in mice and human OI bones have shown that excessive activation of TGF-β signaling plays an important role in dominant and recessive OI disease progression. Inhibition of TGF-β signaling with a murine pan-specific TGF-β neutralizing antibody (1D11) was shown to significantly increase trabecular bone volume and long bone strength in mouse models of OI. To investigate the frequency of dosing and dose options of TGF-β neutralizing antibody therapy, we assessed the effect of 1D11 on disease progression in a dominant OI mouse model (

Indexed as

BIOCHEMICAL MARKERS OF BONE TURNOVEROSTEOBLASTSOSTEOCLASTSOSTEOGENESIS IMPERFECTATGF‐β

Identifiers

PMID34532615
PMCPMC8441395
OpenAlexW3173697488

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.