Evidence map›Paper›PMID 26161291›Full record

ArticleBone research2015

Administration of soluble activin receptor 2B increases bone and muscle mass in a mouse model of osteogenesis imperfecta.

Douglas J DiGirolamo, Vandana Singhal, Xiaoli Chang, Se-Jin Lee, Emily L Germain-Lee

Abstract read
In one paragraph

Article in Bone research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
–field-weighted citation impact
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

40 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Rethinking Osteoporosis Drugs: Can We Simultaneously Address Sarcopenia?International journal of molecular sciences · 2025
    Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. Myostatin: A Skeletal Muscle Chalone.Annual review of physiology · 2023
    Review
  10. Combinatorial Inhibition of Myostatin and Activin A Improves Femoral Bone Properties in the G610C Mouse Model of Osteogenesis Imperfecta.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Impact of Genetic and Pharmacologic Inhibition of Myostatin in a Murine Model of Osteogenesis Imperfecta.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2021
    Article
  18. Review
  19. Article
  20. Review
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.

Douglas J DiGirolamoDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine , Baltimore, MD, USA.
Vandana SinghalDepartment of Orthopaedic Surgery, Johns Hopkins University School of Medicine , Baltimore, MD, USA.
Xiaoli ChangBone & Osteogenesis Imperfecta Department, Kennedy Krieger Institute , Baltimore, MD, USA ; Department of Molecular Biology and Genetics, Johns Hopkins University School of Medicine , Baltimore, MD, USA.
Se-Jin LeeDepartment of Molecular Biology and Genetics, Johns Hopkins University School of Medicine , Baltimore, MD, USA.
Emily L Germain-LeeBone & Osteogenesis Imperfecta Department, Kennedy Krieger Institute , Baltimore, MD, USA ; Department of Pediatrics, Johns Hopkins University School of Medicine , Baltimore, MD, USA.

Funding

Regulation of TGF - (beta) pathways in muscular dystrophy fibrosisP01NS072027 · NINDS · UNIVERSITY OF CHICAGO · PI HEYDEMANN, AHLKE · 2011 to 2015
$6.2M
Characterization of Myostatin and GDF-11R01AR060636 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI LEE, SE-JIN · 2010 to 2020
$3.7M
Activin receptor-based therapies for musculoskeletal diseaseR01AR062074 · NIAMS · JOHNS HOPKINS UNIVERSITY · PI DIGIROLAMO, DOUGLAS JAMES · 2011 to 2015
$2.0M
NIAMS NIH HHS R01 AR060636NIAMS NIH HHS R01 AR062074NINDS NIH HHS P01 NS072027
6 · The paper itself

Abstract

Osteogenesis imperfecta (OI) comprises a group of heritable connective tissue disorders generally defined by recurrent fractures, low bone mass, short stature and skeletal fragility. Beyond the skeletal complications of OI, many patients also report intolerance to physical activity, fatigue and muscle weakness. Indeed, recent studies have demonstrated that skeletal muscle is also negatively affected by OI, both directly and indirectly. Given the well-established interdependence of bone and skeletal muscle in both physiology and pathophysiology and the observations of skeletal muscle pathology in patients with OI, we investigated the therapeutic potential of simultaneous anabolic targeting of both bone and skeletal muscle using a soluble activin receptor 2B (ACVR2B) in a mouse model of type III OI (oim). Treatment of 12-week-old oim mice with ACVR2B for 4 weeks resulted in significant increases in both bone and muscle that were similar to those observed in healthy, wild-type littermates. This proof of concept study provides encouraging evidence for a holistic approach to treating the deleterious consequences of OI in the musculoskeletal system.

Identifiers

PMID26161291
PMCPMC4472144

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Registered trials

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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.