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Graves' Disease: Introducing New Genetic and Epigenetic Contributors Publisher Pubmed



Razmara E1, 2 ; Salehi M3 ; Aslani S1 ; Bitaraf A1, 4 ; Yousefi H5 ; Colon JR5 ; Mahmoudi M1, 6
Authors
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Authors Affiliations
  1. 1. Rheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Australian Regenerative Medicine Institute, Monash University, Clayton, Australia
  3. 3. School of Medicine, Shahrekord University of Medical Science, Iran
  4. 4. Department of Molecular Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran
  5. 5. Department of Biochemistry and Molecular Biology, LSUHSC School of Medicine, New Orleans, LA, United States
  6. 6. Inflammation Research Center, Tehran University of Medical Sciences, Tehran, Iran

Source: Journal of molecular endocrinology Published:2021


Abstract

Autoimmune thyroid disease (AITD) accounts for 90% of all thyroid diseases and affects 2-5% of the population with remarkable familial clustering. Among AITDs, Graves' disease (GD) is a complex disease affecting thyroid function. Over the last two decades, case-control studies using cutting-edge gene sequencing techniques have detected various susceptible loci that may predispose individuals to GD. It has been presumed that all likely associated genes, variants, and polymorphisms might be responsible for 75-80% of the heritability of GD. As a result, there are implications concerning the potential contribution of environmental and epigenetic factors in the pathogenesis of GD, including its initiation, progression, and development. Numerous review studies have summarized the contribution of genetic factors in GD until now, but there are still some key questions and notions that have not been discussed concerning the interplay of genetic, epigenetic, and immunological factors. With this in mind, this review discusses some newly-identified loci and their potential roles in the pathogenicity of GD. This may lead to the identification of new, promising therapeutic targets. Here, we emphasized principles, listed all the reported disease-associated genes and polymorphisms, and also summarized the current understanding of the epigenetic basis of GD.