Evidence map›Paper›PMID 38255829›Full record

ArticleInternational journal of molecular sciences2024

Cilostazol Stimulates Angiogenesis and Accelerates Fracture Healing in Aged Male and Female Mice by Increasing the Expression of PI3K and RUNX2.

Maximilian M Menger, Maximilian Emmerich, Claudia Scheuer, Sandra Hans, Sabrina Ehnert, Andreas K Nüssler, Steven C Herath, Konrad Steinestel, Michael D Menger, Tina Histing and 1 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
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  5. International journal of molecular sciences · 2024
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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

11 authors at 2 institutions in 1 country.

Maximilian M MengerDepartment of Trauma and Reconstructive Surgery, BG Trauma Center Tuebingen, Eberhard Karls University Tuebingen, 72076 Tuebingen, Germany.ORCID 0000-0002-1261-9877
Maximilian EmmerichInstitute for Clinical and Experimental Surgery, Saarland University, 66421 Homburg, Germany.
Claudia ScheuerInstitute for Clinical and Experimental Surgery, Saarland University, 66421 Homburg, Germany.
Sandra HansInstitute for Clinical and Experimental Surgery, Saarland University, 66421 Homburg, Germany.
Sabrina EhnertDepartment of Trauma and Reconstructive Surgery, BG Trauma Center Tuebingen, Siegfried Weller Institute for Trauma Research, Eberhard Karls University Tuebingen, 72076 Tuebingen, Germany.ORCID 0000-0003-4347-1702
Andreas K NüsslerDepartment of Trauma and Reconstructive Surgery, BG Trauma Center Tuebingen, Siegfried Weller Institute for Trauma Research, Eberhard Karls University Tuebingen, 72076 Tuebingen, Germany.ORCID 0000-0002-6666-6791
Steven C HerathDepartment of Trauma and Reconstructive Surgery, BG Trauma Center Tuebingen, Eberhard Karls University Tuebingen, 72076 Tuebingen, Germany.
Konrad SteinestelInstitute of Pathology and Molecular Pathology, Bundeswehrkrankenhaus Ulm, 89081 Ulm, Germany.ORCID 0000-0002-6549-9848
Michael D MengerInstitute for Clinical and Experimental Surgery, Saarland University, 66421 Homburg, Germany.
Tina HistingDepartment of Trauma and Reconstructive Surgery, BG Trauma Center Tuebingen, Eberhard Karls University Tuebingen, 72076 Tuebingen, Germany.
Matthias W LaschkeInstitute for Clinical and Experimental Surgery, Saarland University, 66421 Homburg, Germany.ORCID 0000-0002-7847-8456
Saarland University · DEBundeswehrkrankenhaus · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fracture healing in the aged is associated with a reduced healing capacity, which often results in delayed healing or non-union formation. Many factors may contribute to this deterioration of bone regeneration, including a reduced 'angiogenic trauma response'. The phosphodiesterase-3 (PDE-3) inhibitor cilostazol has been shown to exert pro-angiogenic and pro-osteogenic effects in preclinical studies. Therefore, we herein analyzed in a stable closed femoral fracture model whether this compound also promotes fracture healing in aged mice. Forty-two aged CD-1 mice (age: 16-18 months) were daily treated with 30 mg/kg body weight cilostazol (

Indexed as

Femoral FracturesPhosphatidylinositol 3-KinaseAngiogenesisAnimalsCilostazolCore Binding Factor Alpha 1 SubunitFemaleFracture HealingMaleMicePhosphatidylinositol 3-KinasesPhosphodiesterase 3 InhibitorsX-Ray MicrotomographyCilostazolCore Binding Factor Alpha 1 SubunitPhosphatidylinositol 3-KinasePhosphatidylinositol 3-KinasesPhosphodiesterase 3 InhibitorsRunx2 protein, mouseagingangiogenesiscilostazolfemurfracture healingmicePI3KRUNX2screw

Identifiers

PMID38255829
PMCPMC10815626
OpenAlexW4390671051

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.