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Recent advances in proteomic technologies have enabled systematic analysis of the expression patterns and regulatory mechanisms of these antioxidant enzymes and markers, providing valuable insights into the complex redox regulation within blood 6
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Our results indicated that all the fourteen selected acyl-carnitines with FDR q 1.0 (i.e., C2, C8, C10, C10:1, C10:2, C12, C12:1, C14:1, C14:1-OH, C14:2, C14:2-OH, C16:2, C16:2-OH, and C18) were lower in posttreatment patients after controlling age, sex, BMI, smoking, and drinking (Tables 3 and 4)
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