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Clinical predictors of symptom improvement Binary logistic regression analysis to predict clinical outcomes (with the symptom improvement group coded as 1 and the non-improvement group as 0) included demographic characteristics (age, sex, education), clinical features (BMI, chlorpromazine equivalent dose, duration of illness, age of onset), baseline PANSS total scores, and OS indicators (TGSH, GSSG, GSH, and GSH/GSSG ratio) before and after ECT

This lack of human evidence has led both the FDA and WADA to restrict BPC-157, citing concerns about unregulated use, unknown human toxicity profiles, and potential for misuse [3537]

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