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Protocol overview: BPC-157 administered via subcutaneous injection, locally near the affected joint Standard dosing range: 200500 mcg per injection session Treatment duration: 48 weeks of active treatment Follow-up assessments: 6 months and 12 months post-treatment Patients were evaluated using validated pain scales (VAS and KOOS scores) and functional mobility assessments at each follow-up point

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For example, carriers of the FTO rs9939609 A-allele show altered nutrient storage and appetite circuit sensitivity, benefiting from higher-dose B12 and folate than standard recommendations

This degradation contributes to cartilage breakdown, increased inflammation, and the characteristic pain and stiffness associated with joint problems