The pathogenesis of MTX-induced renal impairment is thought to be mediated by either MTX and its metabolites precipitating in the renal tubules or MTXs direct toxic impact on the renal tubules (Reference Widemann and Adamson6)
Results indicate that the prevalence of intestinal barrier dysfunction is higher in patients with hypertension than in those without hypertension [45, 85,86,87,88]
CYP1A2 displayed stable expression across Days 730, while CYP1B1 and CYP4F12 exhibited progressive increases, reaching maximum levels at Day 45, reflecting roles in fatty acid and bile acid metabolism during later stages
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