ArticleCureus2025
The Future of Osteoarthritis Management: Plasma Exchange as a New Generation Treatment.
Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
- Nutritional metabolic dysregulation in T2DM as a catalyst for osteoarthritis pathogenesis.Frontiers in nutrition · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Osteoarthritis (OA), traditionally viewed as a mechanical wear-and-tear condition, is increasingly recognized as an inflammatory disorder with autoimmune features. Despite its high global prevalence, disease-modifying treatments remain limited. Therapeutic plasma exchange (TPE) offers a novel, mechanistically targeted approach by removing systemic inflammatory mediators, pathogenic autoantibodies, and degradative enzymes such as matrix metalloproteinases. By modulating cytokines like interleukin-1 beta (IL-1β), tumor necrosis factor-alpha (TNF-α), and interleukin-6 (IL-6) and depleting cartilage-directed autoantibodies, TPE may disrupt the inflammatory and immune cascades driving joint degradation. This editorial explores TPE as a potential adjunct therapy in OA, particularly for patients with inflammatory or metabolic phenotypes. While complications such as hypotension, vascular access issues, and transient immunosuppression must be considered, the safety profile of TPE is well-established in other autoimmune conditions. Future clinical trials are urgently needed to validate efficacy, optimize protocols, and identify ideal patient subgroups. If successful, TPE could represent a paradigm shift from symptomatic relief toward disease modification in OA, with the potential to improve long-term outcomes and quality of life.
Indexed as
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What OpenQuestion holds
Registered trials
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.