Twin studies as a model for exploring the aetiology of autoimmune thyroid disease

• Published in: Clinical endocrinology (Oxford) Vol. 76; no. 4; pp. 457 - 464
• Main Authors: Brix, Thomas Heiberg, Hegedüs, Laszlo
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.04.2012; Blackwell; Wiley Subscription Services, Inc
• Subjects: Autoimmune Diseases - etiology; Autoimmune Diseases - immunology; Autoimmune Diseases - metabolism; Biological and medical sciences; Birth Weight - physiology; Endocrinopathies; Fundamental and applied biological sciences. Psychology; Humans; Medical sciences; Non tumoral diseases. Target tissue resistance. Benign neoplasms; Thyroid Diseases - etiology; Thyroid Diseases - immunology; Thyroid Diseases - metabolism; Thyroid. Thyroid axis (diseases); Twin Studies as Topic; Vertebrates: endocrinology; Endocrinopathy; Immunopathology; Etiology; Thyroid diseases; Autoimmune disease; Models; Endocrinology; Twin
• ISSN: 0300-0664; 1365-2265
• DOI: 10.1111/j.1365-2265.2011.04318.x

Summary Twins are an important resource for evaluating the relative contribution of genetic and environmental factors in determining a phenotype. During the last decades, a number of twin studies have investigated the aetiology of several phenotypes related to thyroid autoimmunity. Taken together, these studies have provided valid and unbiased information regarding the influence of genetic and environmental factors in the aetiology of autoimmune thyroid disease (AITD). The comparison of concordance rates between monozygotic (MZ) and dizygotic twins provides irrefutable evidence of a genetic component, and biometric twin modelling shows that approximately 75% of the total phenotypic variance in AITD is because of genetic effects. On the other hand, the lack of complete concordance in MZ twin pairs is proof of environmental and/or epigenetic factors also playing an important role. The impact of environmental triggers such as cigarette smoking, birth characteristics, infection with Yersinia enterocolitica, microchimerism and degree of X chromosome inactivation (XCI) has been evaluated by investigating AITD discordant twin pairs. These studies indicate that smoking, Y. enterocolitica infection and skewed XCI may be causally associated with clinically overt AITD, but not with the presence of thyroid autoantibodies in euthyroid subjects. Microchimerism, but not birth weight, might play a role in AITD. Twin studies offer several features that uniquely enhance our ability to localize genes and understand their function. Future twin studies should incorporate information on genetic, epigenetic and environmental variation thereby enhancing our ability to quantify the precise effect of specific risk factors.