Evidence map›Paper›PMID 38855797›Full record

ArticleJBMR plus2024

Irisin prevents trabecular bone damage and tumor invasion in a mouse model of multiple myeloma.

Roberta Zerlotin, Angela Oranger, Patrizia Pignataro, Manuela Dicarlo, Lorenzo Sanesi, Clelia Suriano, Giuseppina Storlino, Rita Rizzi, Anna Mestice, Sante Di Gioia and 4 more

Abstract read
In one paragraph

Article in JBMR plus, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. 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

14 authors.

Roberta ZerlotinDepartment of Precision and Regenerative Medicine and Ionian Area, University of Bari, 70124 Bari, Italy.
Angela OrangerDepartment of Precision and Regenerative Medicine and Ionian Area, University of Bari, 70124 Bari, Italy.
Patrizia PignataroDepartment of Translational Biomedicine and Neuroscience, University of Bari, 70124 Bari, Italy.
Manuela DicarloDepartment of Precision and Regenerative Medicine and Ionian Area, University of Bari, 70124 Bari, Italy.
Lorenzo SanesiDepartment of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.
Clelia SurianoDepartment of Precision and Regenerative Medicine and Ionian Area, University of Bari, 70124 Bari, Italy.
Giuseppina StorlinoDepartment of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.
Rita RizziDepartment of Precision and Regenerative Medicine and Ionian Area, University of Bari, 70124 Bari, Italy.
Anna MesticeDepartment of Precision and Regenerative Medicine and Ionian Area, University of Bari, 70124 Bari, Italy.
Sante Di GioiaDepartment of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.
Giorgio MoriDepartment of Clinical and Experimental Medicine, University of Foggia, 71122 Foggia, Italy.
Maria GranoDepartment of Precision and Regenerative Medicine and Ionian Area, University of Bari, 70124 Bari, Italy.
Graziana ColaianniDepartment of Precision and Regenerative Medicine and Ionian Area, University of Bari, 70124 Bari, Italy.
Silvia ColucciDepartment of Translational Biomedicine and Neuroscience, University of Bari, 70124 Bari, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Bone disease associated with multiple myeloma (MM) is characterized by osteolytic lesions and pathological fractures, which remain a therapeutic priority despite new drugs improving MM patient survival. Antiresorptive molecules represent the main option for the treatment of MM-associated bone disease (MMBD), whereas osteoanabolic molecules are under investigation. Among these latter, we here focused on the myokine irisin, which is able to enhance bone mass in healthy mice, prevent bone loss in osteoporotic mouse models, and accelerate fracture healing in mice. Therefore, we investigated irisin effect on MMBD in a mouse model of MM induced by intratibial injection of myeloma cells followed by weekly administration of 100 μg/kg of recombinant irisin for 5 wk. By micro-Ct analysis, we demonstrated that irisin improves MM-induced trabecular bone damage by partially preventing the reduction of femur Trabecular Bone Volume/Total Volume (

Indexed as

bone damageirisinmultiple myelomaOpgRankLsclerostin

Identifiers

PMID38855797
PMCPMC11162589

What OpenQuestion holds

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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.