Evidence map›Paper›PMID 40826359›Full record

ArticleJournal of translational medicine2025

Mechanism of action behind the pain-relief effects of extracellular vesicles in microfragmented adipose tissue: an in vitro and in vivo study.

Francesco De Francesco, Letizia Ferroni, Ilaria Zanolla, Lucia Sileo, Maria Pia Cavaleri, Mario Fordellone, Letizia Senesi, Anna Maria Monachino, Elena Tremoli, Ilenia Pia Cappucci and 10 more

Abstract read
In one paragraph

Article in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  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

20 authors.

Francesco De Francesco *Department of Reconstructive Surgery and Hand Surgery, Azienda Ospedaliera Universitaria delle Marche, 60126, Ancona, Italy.
Letizia Ferroni *Maria Cecilia Hospital, GVM Care & Research, 48033, Cotignola, Ravenna, Italy.
Ilaria ZanollaDepartment of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy.
Lucia SileoDepartment of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy.
Maria Pia CavaleriDepartment of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy.
Mario FordelloneDepartment of Mental, Physical Health and Preventive Medicine Campania University L.Vanvitelli, Caserta, Italy.
Letizia SenesiDepartment of Reconstructive Surgery and Hand Surgery, Azienda Ospedaliera Universitaria delle Marche, 60126, Ancona, Italy.
Anna Maria MonachinoDepartment of Reconstructive Surgery and Hand Surgery, Azienda Ospedaliera Universitaria delle Marche, 60126, Ancona, Italy.
Elena TremoliMaria Cecilia Hospital, GVM Care & Research, 48033, Cotignola, Ravenna, Italy.
Ilenia Pia CappucciMaria Cecilia Hospital, GVM Care & Research, 48033, Cotignola, Ravenna, Italy.
Eduardo Maria SommellaDipartimento di Farmacia, Università Degli Studi di Salerno, Fisciano, Italy.
Massimo BonoraDepartment of Medical Sciences, Section of Experimental Medicine, Laboratory for Advanced Therapies (LTTA), University of Ferrara, and Technopole of Ferrara, Ferrara, Italy.
Alfredo RoncaInstitute of Polymers, Composites and Biomaterials - National Research Council (IPCB-CNR), 23900, Lecco, Italy. alfredo.ronca@cnr.it.ORCID 0000-0002-6658-004X
Ugo D'AmoraInstitute of Polymers, Composites and Biomaterials - National Research Council (IPCB-CNR), 80125, Naples, Italy.
Noemi De CesareInstitute of Polymers, Composites and Biomaterials - National Research Council (IPCB-CNR), 80125, Naples, Italy.
Luca LovattiDepartment of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy.
Michele RiccioDepartment of Reconstructive Surgery and Hand Surgery, Azienda Ospedaliera Universitaria delle Marche, 60126, Ancona, Italy.
Ali MobasheriResearch Unit of Health Sciences and Technology, Faculty of Medicine, University of Oulu, Oulu, Finland.
Paolo PintonDepartment of Medical Sciences, Section of Experimental Medicine, Laboratory for Advanced Therapies (LTTA), University of Ferrara, and Technopole of Ferrara, Ferrara, Italy.
Barbara ZavanDepartment of Translational Medicine, University of Ferrara, 44121, Ferrara, Italy. barbara.zavan@unife.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTrapeziometacarpal osteoarthritis (TMC OA) is a prevalent and debilitating condition that impairs hand functionality and reduces quality of life. Current treatments including conservative measures such as splinting and anti-inflammatory medications, as well as surgical interventions often exhibit limited efficacy or involve invasive procedures. Novel therapeutic approaches are necessary to address the pain and functional limitations experienced by affected patients.

methodsThis study investigates the potential of extracellular vesicles (EVs) derived from autologous microfragmented adipose tissue (aMAT) as a minimally invasive treatment for TMC OA. EVs were characterized using morphological, proteomic, and functional analyses, revealing their ability to modulate cellular processes through proteins associated with extracellular matrix organization, wound healing, and inflammation regulation.

resultsFunctional studies demonstrated that EVs modulate calcium signaling and mitochondrial activity, enhancing cellular bioenergetics and mitigating inflammation-induced dysfunction. In a clinical study with 25 patients diagnosed with TMC OA (Eaton Stage II), aMAT-derived EVs demonstrated significant benefits. Pain scores, measured by the numeric rating scale, improved substantially both at rest and during activity. Functional assessments, including the Michigan Hand Outcomes Questionnaire and Kapandji opposition test, showed enhanced hand performance over 12 months. Strength tests indicated marked improvements in pinch grip, with no adverse effects or disease progression observed radiographically.

conclusionsThe findings underscore the potential of aMAT-derived EVs as a novel, effective, and minimally invasive treatment for TMC OA, providing both pain relief and functional recovery. Further randomized trials are necessary to validate these results and investigate broader clinical applications.

trial registrationThis study was conducted in accordance with the ethical principles outlined in the Declaration of Helsinki and adhered to all relevant national and institutional ethical guidelines for research involving human participants. Approval for the study was obtained from the Ethics Committee of Marche Region, protocol n. 154/2021. All participants provided written informed consent before enrollment in the study. They were informed about the study's purpose, procedures, potential risks, and their right to withdraw at any time without consequences. Informed Patient Consent Statement: Informed consent was obtained from all individual participants included in the study, following the guidelines of the Human Research Approval Committee protocol number 2/2019.

Indexed as

Adipose TissueExtracellular VesiclesPainPain ManagementAgedFemaleHumansInflammationMaleMiddle AgedOsteoarthritisAdipose stem cellsMicrofragmented adipose tissue; extracellular vesiclesNon-enzymatic methodRigenera protocolTrapeziometacarpal arthritis

Identifiers

PMID40826359
PMCPMC12362883

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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.