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Review
. 2025 Jul 31:15563316251355551.
doi: 10.1177/15563316251355551. Online ahead of print.

Emerging Use of BPC-157 in Orthopaedic Sports Medicine: A Systematic Review

Affiliations
Review

Emerging Use of BPC-157 in Orthopaedic Sports Medicine: A Systematic Review

Nikhil Vasireddi et al. HSS J. .

Abstract

Background: Body protection compound-157 (BPC-157) is a naturally occurring gastric peptide that promotes mucosal integrity and homeostasis. Preclinical studies show its potential for promoting healing in musculoskeletal injuries such as fractures, tendon ruptures, ligament tears, and muscle injuries. Despite lacking US Food and Drug Administration approval and its use being banned in professional sports, it is increasingly used by clinicians and athletes. Purpose: We sought to (1) provide a comprehensive synthesis of the BPC-157 literature from an orthopedic sports medicine perspective and (2) elucidate the mechanism of action, musculoskeletal effects, metabolism, and safety profile. Methods. We conducted a systematic review of English-language literature, published from database inception to June 3, 2024, from PubMed, Cochrane, and Embase. We searched PROSPERO to identify any current or unpublished reviews. Studies reporting BPC-157's mechanism, musculoskeletal outcomes, metabolism, and safety were included. Articles were screened in 3 phases by 2 reviewers. In cases of a disagreement between the 2 reviewers, blinding was removed, and eligibility was determined by group consensus, with a third author making the final decision. Results. A total of 544 articles from 1993 to 2024 were identified. After duplicates were removed, 36 studies were included (35 preclinical studies, 1 clinical study). The studies suggest that BPC-157 enhances growth hormone receptor expression and several pathways involved in cell growth and angiogenesis, while reducing inflammatory cytokines. In preclinical models, BPC-157 improved functional, structural, and biomechanical outcomes in muscle, tendon, ligament, and bony injuries. In a retrospective study of musculoskeletal pain following intraarticular injection of BPC-157 for unspecified chronic knee pain, 7 of 12 patients reported relief for >6 months. BPC-157 is metabolized in the liver, with a half-life of less than 30 minutes, and is cleared by the kidneys. Preclinical safety studies showed no adverse effects across several organ systems. No clinical safety data were found. Conclusion: This systematic review of level IV and level V studies suggests that BPC-157 shows promise for promoting recovery from musculoskeletal injuries. Adverse effects are possible due to unregulated manufacturing, contamination, or unknown clinical safety. We recommend that clinicians counsel athletes to understand their organizations' rules to remain compliant with medication/supplement safety and testing standards.

Keywords: BPC-157; athlete; body protection compound-157; gastric pentadecapeptide; orthobiologics; peptide; sports.

Plain language summary

Review of the Musculoskeletal Literature Surrounding a Relatively Novel Peptide, Body Protection Compound-157 Body protection compound-157 (BPC-157) is a naturally occurring substance in the body that helps maintain healthy tissues and organs. Even though it is not approved by the US Food and Drug Administration and is banned in some sports, BPC-157 is still being used. This study aimed to review all the research on BPC-157 to understand how it works, its effects on muscles and joints, how the body processes it, and whether it is safe. The review looked at 36 studies published from 1993 to 2024. The findings showed that BPC-157 helps promote healing by boosting growth factors and reducing inflammation. It has improved outcomes in muscle, tendon, ligament, and bone injury models in animals. In one human study, 7 out of 12 people with chronic knee pain felt relief for over six months after receiving one BPC-157 knee injection. Animal studies showed no harmful effects, but there is no clinical safety data in humans. Overall, BPC-157 could help heal musculoskeletal injuries, but there are potential risks due to unregulated production and lack of clinical safety data.

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Conflict of interest statement

The author(s) declared the following potential conflicts of interest with respect to the research, authorship, and/or publication of this article: Michael J. Salata, MD, declares a relationship with Stryker. Michael Karns, MD, declares relationships with Smith & Nephew and Arthrex. Jacob G. Calcei, MD, declares a relationship with Smith & Nephew. James E. Voos, MD, declares relationships with Arthrex and Mitek. The other authors declare no potential conflicts of interest.

Figures

The diagram illustrates the PRISMA flowchart used in the systematic review. It starts with records identified from databases like PubMed, Embase, and Cochrane Library, totaling 544 records. Out of these, 151 duplicates were removed, leaving 393 records screened. Subsequently, 336 records were manually excluded, and further assessment for eligibility excluded 21 full-text articles. Ultimately, 36 studies were included in the review.
Fig. 1.
PRISMA diagram.
High-level overview of pathways modulated by BPC-157. Notable mediators include VEGF, ERK1/2, FAK, KRAS, AKT, NOS, COX2, MPO, IL-6, TNF-α.
Fig. 2.
High-level overview of pathways modulated by BPC-157. It is important to note that these pathways are nonlinear and often interconnected. VEGF vascular endothelial growth factor; ERK1/2 extracellular signal-regulated kinase 1/2; FAK focal adhesion kinase; KRAS Kirsten rat sarcoma virus; AKT alpha serine/threonine-protein kinase; NOS nitric oxide synthase; COX2 cyclooxygenase-2; MPO myeloperoxidase; IL-6 interleukin-6; TNF-α tumor necrosis factor-alpha.

References

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