Frequency
Graves' disease affects about 1 in 200 people. The disease occurs more often in women than in men, which may be related to hormonal factors. Graves' disease is the most common cause of thyroid overactivity (hyperthyroidism) in the United States.
Causes
Graves' disease is thought to result from a combination of genetic and environmental factors. Some of these factors have been identified, but many remain unknown.
Graves' disease is classified as an autoimmune disorder, one of a large group of conditions that occur when the immune system attacks the body's own tissues and organs. In people with Graves' disease, the immune system creates a protein (antibody) called thyroid-stimulating immunoglobulin (TSI). TSI signals the thyroid to increase its production of hormones abnormally. The resulting overactivity of the thyroid causes many of the signs and symptoms of Graves' disease. Studies suggest that immune system abnormalities also underlie Graves' ophthalmopathy and pretibial myxedema.
People with Graves' disease have an increased risk of developing other autoimmune disorders, including rheumatoid arthritis, pernicious anemia, systemic lupus erythematosus, Addison disease, celiac disease, type 1 diabetes, and vitiligo.
Variations in many genes have been studied as possible risk factors for Graves' disease. Some of these genes are part of a family called the human leukocyte antigen (HLA) complex. The HLA complex helps the immune system distinguish the body's own proteins from proteins made by foreign invaders (such as viruses and bacteria). Other genes that have been associated with Graves' disease help regulate the immune system or are involved in normal thyroid function. Most of the genetic variations that have been discovered are thought to have a small impact on a person's overall risk of developing this condition.
Other, nongenetic factors are also believed to play a role in Graves' disease. These factors may trigger the condition in people who are at risk, although the mechanism is unclear. Potential triggers include changes in sex hormones (particularly in women), viral or bacterial infections, certain medications, and having too much or too little iodine (a substance critical for thyroid hormone production). Smoking increases the risk of eye problems and is associated with more severe eye abnormalities in people with Graves disease.
Inheritance
The inheritance pattern of Graves' disease is unclear because many genetic and environmental factors appear to be involved. However, the condition can cluster in families, and having a close relative with Graves' disease or another autoimmune disorder likely increases a person's risk of developing the condition.
Other Names for This Condition
- Autoimmune hyperthyroidism
- Basedow disease
- Basedow's disease
- Exophthalmic goiter
- Graves' disease
- Toxic diffuse goiter
Additional Information & Resources
Genetic Testing Information
Patient Support and Advocacy Resources
Clinical Trials
Catalog of Genes and Diseases from OMIM
Scientific Articles on PubMed
References
- Eschler DC, Hasham A, Tomer Y. Cutting edge: the etiology of autoimmune thyroid diseases. Clin Rev Allergy Immunol. 2011 Oct;41(2):190-7. doi: 10.1007/s12016-010-8245-8. Citation on PubMed or Free article on PubMed Central
- Hasham A, Tomer Y. Genetic and epigenetic mechanisms in thyroid autoimmunity. Immunol Res. 2012 Dec;54(1-3):204-13. doi: 10.1007/s12026-012-8302-x. Citation on PubMed or Free article on PubMed Central
- Jacobson EM, Huber A, Tomer Y. The HLA gene complex in thyroid autoimmunity: from epidemiology to etiology. J Autoimmun. 2008 Feb-Mar;30(1-2):58-62. doi: 10.1016/j.jaut.2007.11.010. Epub 2008 Jan 4. Citation on PubMed or Free article on PubMed Central
- National Institute of Diabetes and Digestive and Kidney Diseases
- Simmonds MJ, Gough SC. The search for the genetic contribution to autoimmune thyroid disease: the never ending story? Brief Funct Genomics. 2011 Mar;10(2):77-90. doi: 10.1093/bfgp/elq036. Citation on PubMed
- Tomer Y. Genetic susceptibility to autoimmune thyroid disease: past, present, and future. Thyroid. 2010 Jul;20(7):715-25. doi: 10.1089/thy.2010.1644. Citation on PubMed or Free article on PubMed Central
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