Evidence map›Paper›PMID 34173706›Full record

ArticleJournal of biomedical materials research. Part A2021

Endogenous FGF-2 levels impact FGF-2/BMP-2 growth factor delivery dosing in aged murine calvarial bone defects.

Liisa T Kuhn, Tao Peng, Gloria Gronowicz, Marja M Hurley

Open access · greenAbstract read
In one paragraph

Article in Journal of biomedical materials research. Part A, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Liisa T KuhnDepartment of Biomedical Engineering, University of Connecticut Health Center, Farmington, Connecticut, USA.
Tao PengDepartment of Biomedical Engineering, University of Connecticut Health Center, Farmington, Connecticut, USA.
Gloria GronowiczDepartment of Surgery, University of Connecticut Health Center, Farmington, Connecticut, USA.
Marja M HurleyDepartment of Medicine, University of Connecticut Health Center, Farmington, Connecticut, USA.
UConn Health · US

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
Action of Anbolic Factors on Bone Formation in MiceR01AG021189 · NIA · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI HURLEY, MARJA MARIE · 2004 to 2013
$2.5M
FGF2 Isoforms in Bone and Phosphate HomeostasisR01AR072985 · NIAMS · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI HURLEY, MARJA MARIE · 2018 to 2022
$1.8M
NIAMS NIH HHS R01 AR072985NIA NIH HHS R01 AG021189NIA NIH HHS RO1AG021189-A1NIDCR NIH HHS R01 DE021103NIDCR NIH HHS R01DE021103
6 · The paper itself

Abstract

Bone repair in elderly mice has been shown to be improved or negatively impacted by supplementing the highly osteogenic bone morphogenetic protein-2 (BMP-2) with fibroblast growth factor-2 (FGF-2). To better predict the outcome of FGF-2 supplementation, we investigated whether endogenous levels of FGF-2 play a role in optimal dosing of FGF-2 for augmenting BMP-2 activity in elderly mice. In vivo calvarial bone defect studies in Fgf2 knockout mice with wildtype controls were conducted with the growth factors delivered in a highly localized manner from a biomimetic calcium phosphate/polyelectrolyte multilayer coating applied to a bone graft substitute. Endogenous FGF-2 levels were measured in old mice versus young and found to decrease with age. Optimal dosing for improving bone defect repair correlated with levels of endogenous FGF-2, with a larger dose of FGF-2 required to have a positive effect on bone healing in the Fgf2 knockout mice. The same dose in wildtype old mice, with higher levels of FGF-2, promoted chondrogenesis and increased osteoclast activity. The results suggest a personalized medicine approach, based on a knowledge of endogenous levels of FGF-2, should guide FGF-2 supplementation in order to avoid provoking excessive bone resorption and cartilage formation, both of which inhibited calvarial bone repair.

Indexed as

AgingAnimalsBiomimeticsBone and BonesBone Morphogenetic Protein 2Bone ResorptionBone TransplantationCalcium PhosphatesCartilageCoated Materials, BiocompatibleDrug Delivery SystemsFemaleFibroblast Growth Factor 2Fracture HealingMiceMice, KnockoutBmp2 protein, mouseBone Morphogenetic Protein 2calcium phosphateCalcium PhosphatesCoated Materials, BiocompatibleFibroblast Growth Factor 2BMP-2bone regenerationcalcium phosphateFGF-2growth factor delivery

Identifiers

PMID34173706
PMCPMC9943554
OpenAlexW3173608642

What OpenQuestion holds

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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.