GSTM1 Gene, Diet, and Kidney Disease: Implication for Precision Medicine? Recent Advances in Hypertension

In the United States, the prevalence of chronic kidney disease in adults is approximate to 14%. The mainstay of therapy for chronic kidney disease is angiotensin-converting enzyme inhibitors or angiotensin receptor blockers, but many patients with chronic kidney disease still progress to end-stage kidney disease. Increased oxidative stress is a major molecular underpinning of chronic kidney disease progression. In humans, a common deletion variant of the glutathione-S-transferase mu-1 (GSTM1) gene, the GSTM1 null allele (GSTM1(0)), results in decreased GSTM1 enzymatic activity and is associated with higher levels of oxidative stress. GSTM1 belongs to the superfamily of GSTs that are phase II antioxidant enzymes and are regulated by Nrf2 (nuclear factor erythroid 2-related factor 2). Cruciferous vegetables in general, and broccoli in particular, are rich in glucoraphanin, a precursor of sulforaphane that has been shown to have protective effects against oxidative damage through the activation of Nrf2. This review will highlight recent human and animal studies implicating the role of GSTM1 deficiency in hypertension and kidney disease, and its impact on the effects of cruciferous vegetables on kidney injury and disease progression, illustrating the significance of gene and environment interaction and a potential for targeted precision medicine in the treatment of kidney disease.

Automated summary

This passage discusses the prevalence and treatment of chronic kidney disease in the United States, as well as the impact of oxidative stress on disease progression. Research suggests that deficiency of GSTM1 is associated with increased oxidative stress levels, while a component in cruciferous vegetables can exert protective effects against oxidative damage through Nrf2 activation.