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While several studies examined GPx activity [63, 71, 72, 74, 81, 83, 84] or its polymorphisms [94, 95], only one examined glutathione reductase or glutathione-S-transferase activity [85]

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Although the exact etiology remains unknown, current evidence points to a significant genetic component in the development and severity of FM which can be associated with a spectrum of diseases, including infections, diabetes, rheumatic diseases, and psychiatric or neurological comorbidities [6]

[DOI] [PMC free article] [PubMed] [Google Scholar] 95.Iriyama N., Miura K., Uchino Y., et al

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