Epigenetic and Diabetes Mellitus Type 1

Abstract

Type 1 diabetes mellitus (T1D) is one of the commonest chronic autoimmune diseases. It’s characterized by formation of islet specific T cells and autoantibodies leading to chronic inflammation in the islelets, i.e. inflammatory destruction of the β cells resulting in an insulin deficiency. T1D resulting from the interplay of genetic, epigenetic, and environmental factors. Worldwide, the T1D epidemic represents an increasing global public health burden,Egypt ranked 8th highest in the world. The incidence of T1D among the children has been rising. There has been an overall increase in the incidence of T1D of 3% to 5% per year. Suggested the interaction between genetic predisposition and environmental factors. The low disease concordance rate in adult-onset T1D ( 80 % of pancreatic β cells are destroyed. miRNA 375 easily detectable can detected blood, can found in serum, plasma and urine. Also miRNA 375is stable even against boiling low or high pH, multiple freeze throw cycle. Diane Mathis, Benoist and co-worker at Harvard medical school and GlaxoSmithKline reported that an epigenetic drug called BET151 can effectively prevent T1D in mouse model for these diseases. This is by neutralizing the cytokines, blocking the interaction of T cells and antigen presenting cell and regeneration of β cells. A novel epigenetic drugs for treatment of T1D by transdifferantiation of human dermal fibroblasts into insulin cell producing cells by inducing the expression of insulin through increasing acetylation and decrease methylation by two epigenetic modified compounds romidepsin a histone deacetylase inhibitor and Azacytidine that cant methylated.