Evidence map›Paper›PMID 25681640›Full record

ArticleExperimental gerontology2015

Effects of low dose FGF-2 and BMP-2 on healing of calvarial defects in old mice.

Lyndon F Charles, Jessica L Woodman, Daisuke Ueno, Gloria Gronowicz, Marja M Hurley, Liisa T Kuhn

Open access · greenAbstract read
In one paragraph

Article in Experimental gerontology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
7.0field-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.

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

33 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Role of FGF2 in promoting osteogenic differentiation for craniofacial bone regeneration.Regenerative engineering and translational medicine · 2025
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. The role of proteoglycan form of DMP1 in cranial repair.BMC molecular and cell biology · 2022
    Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Review
  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

6 authors at 2 institutions in 2 countries.

Lyndon F CharlesDepartment of Reconstructive Sciences, University of Connecticut Health Center, Farmington, CT 06030, USA.
Jessica L WoodmanDepartment of Reconstructive Sciences, University of Connecticut Health Center, Farmington, CT 06030, USA.
Daisuke UenoUnit of Oral and Maxillofacial Implantology, Tsurumi University School of Dental Medicine, Yokohama, Japan.
Gloria GronowiczDepartment of Surgery, University of Connecticut Health Center, Farmington, CT 06030, USA.
Marja M HurleyDepartment of Medicine, University of Connecticut Health Center, Farmington, CT 06030, USA.
Liisa T KuhnDepartment of Reconstructive Sciences, University of Connecticut Health Center, Farmington, CT 06030, USA. Electronic address: lkuhn@uchc.edu.
UConn Health · USTsurumi University · JP

Funding

Modulated release of growth factors for stimulating progenitors in aging boneR01DE021103 · NIDCR · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI KUHN, LIISA TIINA · 2012 to 2025
$4.4M
NIDCR NIH HHS R01 DE021103NIDCR NIH HHS R01DE021103
6 · The paper itself

Abstract

There is an age-associated reduction in the bone healing activity of bone morphogenetic protein-2 (BMP-2) that is currently addressed by administering higher doses of BMP-2 in elderly patients. The unwanted medical complications from high dose BMP-2 motivated this investigation to determine whether the addition of a low dose of fibroblast growth factor 2 (FGF-2) could enhance the ability of a lower dose of BMP-2 to heal calvarial bone defects in old mice (18-20 months old). FGF-2 (5 ng) and BMP-2 (2 μg) were administered by a controlled release two-phase biomaterial scaffold placed into the bone defect. FGF-2 released more rapidly and completely in vitro than BMP-2 (40% vs 2%). In vivo, both BMP-2 and FGF-2+BMP-2 groups formed more new bone in calvarial defects than scaffold alone (p < 0.001) or FGF-2 only groups (p < 0.01). The overall total volume of new bone was not statistically increased by the addition of FGF-2 to BMP-2 as measured by microCT, but the pattern of bone deposition was different. In old mice, but not young, there was enhanced bony fill in the central bone defect area when the BMP-2 was supplemented with FGF-2. Histological analysis of the center of the defect revealed an increased bone volume (%BV/TV (p = 0.004)) from the addition of FGF-2. These studies suggest that combining a low dose of FGF-2 with a low dose of BMP-2 has the potential to increase bone healing in old mice relative to BMP-2 alone.

Indexed as

AgingAnimalsBone Morphogenetic Protein 2Bone RegenerationFemaleFibroblast Growth Factor 2MiceMice, Inbred BALB COsteogenesisSkullWound HealingX-Ray MicrotomographyBone Morphogenetic Protein 2Fibroblast Growth Factor 2

Identifiers

PMID25681640
PMCPMC4388203
OpenAlexW2043473344

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.