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When cells are subjected to oxidative stress, Nrf2 dissociates from Keap1 and moves to the nucleus to bind to the promoter of HO-1, promoting the transcription and expression of HO-1 [10]

Animal studies confirm: offspring of caffeine-exposed rats showed abnormal methylation patterns on genes controlling adrenal hormone production, with 51.2% born growth-restricted.[28] Most alarming: these epigenetic effects carried forward into grandchildren never exposed to caffeine themselves.[17] Your Genes Determine Your Risk The CYP1A2 gene has a well-studied polymorphism (rs762551)