Evidence map›Paper›PMID 40685948›Full record

ArticleJournal of orthopaedic research : official publication of the Orthopaedic Research Society2025

Osteogenic Small Molecule FK506 for Enhanced Bone Formation in a Rabbit Ankle Fusion Model.

Nicholas Huffman, Amogh Magesh, Hanna Solomon, Caroline Dingler, Sreedhara Sangadala, Jay M Patel, Jason T Bariteau

Abstract read
In one paragraph

Article in Journal of orthopaedic research : official publication of the Orthopaedic Research Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Nicholas HuffmanDepartment of Orthopaedics, Emory University School of Medicine, Atlanta, Georgia, USA.
Amogh MageshDepartment of Orthopaedics, Emory University School of Medicine, Atlanta, Georgia, USA.
Hanna SolomonDepartment of Orthopaedics, Emory University School of Medicine, Atlanta, Georgia, USA.
Caroline DinglerDepartment of Orthopaedics, Emory University School of Medicine, Atlanta, Georgia, USA.
Sreedhara SangadalaDepartment of Orthopaedics, Emory University School of Medicine, Atlanta, Georgia, USA.
Jay M PatelDepartment of Orthopaedics, Emory University School of Medicine, Atlanta, Georgia, USA.ORCID 0000-0003-4889-0818
Jason T BariteauDepartment of Orthopaedics, Emory University School of Medicine, Atlanta, Georgia, USA.

Funding

This study was supported by American Orthopaedic Foot and Ankle Society (2022-21964-E).
6 · The paper itself

Abstract

Non-union remains a significant complication following ankle fusion procedures, underscoring the need for effective osteogenic adjuvants to improve boney healing and fusion outcomes. This study investigates the osteogenic potential of FK506 (Tacrolimus), both in vitro and in vivo, for enhanced ankle fusion. Known orthobiologics in the market, such as recombinant human platelet-derived growth factor-BB (rhPDGF-BB), have been utilized to promote bone healing and were included in this study to assess their comparative and combinatory effects with FK506. Bovine marrow-derived cells (MDCs) were cultured in 2D and 3D environments to assess temporal markers of osteogenesis: RUNX2 nuclear localization (early), Alizarin Red S staining (intermediate), and mineral deposition with micro-computed tomography (late). A rabbit ankle fusion model (t = 4 weeks) was utilized to evaluate FK506's early in vivo efficacy. In 2D cultures, FK506 resulted in an increase, but rhPDGF-BB and the combination of rhPDGF-BB and FK506 yielded the highest mineral deposition. However, in 3D fibrin gel cultures, FK506 alone demonstrated the greatest bone volume and tissue mineralization. In vivo rabbit ankle studies revealed that while ankle joint fusion was not achieved, FK506-treated animals consistently showed substantial bone formation anterior to the joint, indicating its potential for localized osteogenesis in the ankle environment. This study demonstrates FK506's osteogenic potential as a standalone or combinatorial therapy. These findings highlight the need for further optimization of FK506 delivery methods and fixation strategies to maximize its clinical utility in ankle fusion procedures. Statement of Clinical Significance: The investigation of FK506 represents a potential pharmacological strategy for enhancing fusion healing and improving patient outcomes.

Indexed as

Calcineurin InhibitorsFracture HealingFractures, MalunitedOsteogenesisTacrolimusAngiogenesis Inducing AgentsAnimalsAnkle FracturesArthrodesisBecaplerminCalcification, PhysiologicCells, CulturedModels, AnimalPostoperative ComplicationsRabbitsTreatment OutcomeAngiogenesis Inducing AgentsBecaplerminCalcineurin InhibitorsTacrolimusankle fusionnon‐unionosteogenesisTacrolimus

Identifiers

PMID40685948
PMCPMC12422209

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.