Downregulation of SOD1 in vitro and in vivo models has been associated with neuronal death [61], while overexpression of SOD1 in transgenic mice has been associated with protection of the cerebral tissue in several pathological conditions such as ischemia or Parkinson’s disease Lowered SOD activity has been linked to a high risk of oxidative stress, which can lead to a number of diseases, ranging including diabetes, heart failure, stroke, hypertension, high cholesterol, and atherosclerosis [14,62]. The gene discussed is SOD1; the disease is heart failure.