ReviewFrontiers in surgery2026
Adipose-derived mesenchymal stem cells for early hip osteoarthritis: mechanistic insights and possible clinical evidence.
Review in Frontiers in surgery, 2026. 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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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.
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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.
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0 citing papers in PubMed.
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Authors and funding
9 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Purpose: Hip osteoarthritis (OA) is increasingly diagnosed in younger, active patients, often linked to femoroacetabular impingement (FAI) and associated cartilage lesions such as acetabular delamination. Conventional surgical options, including total hip arthroplasty, are suboptimal in this population due to implant longevity concerns and high functional demands. Adipose-derived mesenchymal stem cells (AD-MSCs) have emerged as a promising biologic alternative, offering regenerative, anti-inflammatory, and immunomodulatory effects with advantages over bone marrow-derived MSCs in cell yield, harvesting ease, and safety. Methods: We conducted a review of the literature on the possible use of mesenchymal as a treatment for hip osteoarthritis. Results: Processed via manipulative mechanical techniques, AD-MSCs can be delivered intra-articularly to target early- stage OA and focal cartilage damage, aiming to preserve joint integrity and delay progression. Clinical studies report improvements in pain, function, and quality of life, with low complication rates, particularly in Tönnis grade 1 hips. Acetabular delamination, an early and potentially reversible chondral lesion, represents a compelling therapeutic target for biologic intervention. Conclusion: This new possible therapy will be a new minimally invasive option for joint-preservation, in particular for young patients. Limitations include heterogeneity in protocols, lack of standardized dosing, and scarce long-term randomized evidence. Future research should focus on optimized delivery methods, patient selection, and high-quality trials to establish AD-MSCs as a validated component of hip preservation strategies. Clinical trials are needed to confirm their efficacy and long-term benefits.
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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.