Evidence map›Paper›PMID 39633422›Full record

Trial reportJournal of translational medicine2024

Posterior iliac crest vs. proximal tibia: distinct sources of anti-inflammatory and regenerative cells with comparable 6-month clinical outcomes in treatment of osteoarthritis.

E Mormone, L Savastano, G Rossi, F Maruccia, G Di Maggio, N P Sinisi, M Sandri, M Copetti, E De Santis, V Guerra and 5 more

Abstract readRandomized Controlled TrialComparative Study
In one paragraph

Trial report in Journal of translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

15 authors.

E MormoneInstitute for Stem Cell Biology, Regenerative Medicine and Innovative Therapies (ISBReMIT), Fondazione IRCCS "Casa Sollievo Della Sofferenza", Viale Padre Pio, 7, 71013, San Giovanni Rotondo, FG, Italy. emormone@yahoo.com.ORCID 0000-0001-5901-3760
L SavastanoDepartment of Orthopedics and Trauma Surgery, Fondazione IRCCS "Casa Sollievo Della Sofferenza", Viale Dei Cappuccini 1, 71013, San Giovanni Rotondo, FG, Italy.
G RossiDepartment of Hematology and Stem Cell Transplant Unit, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Cappuccini, 1, 71013, San Giovanni Rotondo, FG, Italy.
F MarucciaDepartment of Orthopedics and Trauma Surgery, Fondazione IRCCS "Casa Sollievo Della Sofferenza", Viale Dei Cappuccini 1, 71013, San Giovanni Rotondo, FG, Italy.
G Di MaggioDepartment of Orthopedics and Trauma Surgery, Fondazione IRCCS "Casa Sollievo Della Sofferenza", Viale Dei Cappuccini 1, 71013, San Giovanni Rotondo, FG, Italy.
N P SinisiDepartment of Hematology and Stem Cell Transplant Unit, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Cappuccini, 1, 71013, San Giovanni Rotondo, FG, Italy.
M SandriBig and Open Data Innovation Laboratory (BODaI-Lab), University of Brescia, Brescia, Italy.
M CopettiUnit of Biostatistics, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Cappuccini, 71013, San Giovanni Rotondo, Italy.
E De SantisInstitute for Stem Cell Biology, Regenerative Medicine and Innovative Therapies (ISBReMIT), Fondazione IRCCS "Casa Sollievo Della Sofferenza", Viale Padre Pio, 7, 71013, San Giovanni Rotondo, FG, Italy.
V GuerraInstitute for Stem Cell Biology, Regenerative Medicine and Innovative Therapies (ISBReMIT), Fondazione IRCCS "Casa Sollievo Della Sofferenza", Viale Padre Pio, 7, 71013, San Giovanni Rotondo, FG, Italy.
G BiancofioreUnit of Pathology, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Dei Cappuccini 1, 71013, San Giovanni Rotondo, FG, Italy.
C CisterninoUnit of Transfusion Medicine and Laboratory, Fondazione IRCCS Casa Sollievo Della Sofferenza, Viale Cappuccini 1, 71013, San Giovanni Rotondo, Italy.
E CaradonnaIntegrated Laboratory Medicine Services, Centro Diagnostico, Milan, Italy.
P GrazianoDepartment of Radiological, Oncological and Pathological Sciences, Sapienza University of Rome, Rome, Italy.
F L GorgoglioneDepartment of Orthopedics and Trauma Surgery, Fondazione IRCCS "Casa Sollievo Della Sofferenza", Viale Dei Cappuccini 1, 71013, San Giovanni Rotondo, FG, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman bone marrow is a source of mesenchymal stem cells (MSCs), other progenitor cells, and factors with anti-inflammatory and regenerative capacity. Though the fraction of MSCs out of the nucleated cells is very small, bone marrow aspirate (BMA) for osteoarthritis (OA) has noteworthy effects. BMA is usually collected from the posterior or anterior iliac crest, and rarely from the proximal tibia. We investigated the clinically beneficial concentration of ex vivo MSCs, derived from BM harvested from the posterior iliac crest and proximal tibia by Marrow Cellution™ Aspiration System, and their phenotypic differences, in comparison to autologous Platelet-Rich Plasma (PRP) treatment prepared with a manual, closed system.

methodsA single-center, parallel, randomized controlled study was designed to investigate the efficacy of BMA from the posterior iliac crest compared to BMA from the proximal tibia, against a control group treated with PRP, in knee OA. Thirty patients with knee OA grade I-IV, according to Kellgren-Lawrence (KL), were distributed into each group. Visual Analog Scale (VAS) and Western Ontario & McMaster Universities Arthritis Index (WOMAC) score were used for clinical outcome evaluation.

resultsData from an intermediate analysis of 6-months follow-up, involving 15 patients in each arm, showed that the posterior iliac crest was significantly more densely populated with mononuclear cells, than the proximal tibia (p = 0.005). Flow cytometric analysis on ex vivo BMA showed a significantly greater number of MSCs in the BM-derived from the posterior iliac crest when compared with the proximal tibia (p < 0.001), together with a significantly higher number of platelets (PLTs) (p < 0.001). Surprisingly, despite these differences in cells number, the improvement in early pain and function scores, after each treatment, were statistically significant within each of the three arms. BM from the proximal tibia showed the highest ΔWOMAC, while BM from the posterior iliac crest showed the highest ΔVAS; however, these differences were not statistically significant across the three arms (p > 0.05). A better outcome, in terms of ΔVAS, was observed in patients classified as KL I-II, when treated with BMA from crest (p < 0.001) and PRP (p = 0.004). Moreover, the effect of BMA treatment on ΔVAS depends on MSCs % only in the Tibia Arm (r = -0.59, p = 0.021), where we also found a correlation between ΔWOMAC and monocytes (r = 0.75, p = 0.016).

conclusionThe results indicate that the iliac crest yields a higher concentration of MSCs compared to the proximal tibia, however both BM, independently of the MSCs concentration, show a beneficial clinical outcome in the treatment of knee OA. Furthermore, BMA is not superior to PRP treatment.

Indexed as

IliumOsteoarthritisTibiaAgedAnti-Inflammatory AgentsFemaleHumansMaleMesenchymal Stem CellsMiddle AgedPlatelet-Rich PlasmaRegenerationTreatment OutcomeAnti-Inflammatory Agents

Identifiers

PMID39633422
PMCPMC11616267

What Socratic holds

Textmetadata
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.