Thyroid autoimmunity and polyglandular endocrine syndromes

被引:0
作者
Jean-Louis Wémeau
Emmanuelle Proust-Lemoine
Amélie Ryndak
Laura Vanhove
机构
[1] Service d’Endocrinologie et des Maladies Métaboliques,Clinique Endocrinologique Marc Linquette
[2] Hôpital Claude Huriez,undefined
[3] 4ème Ouest,undefined
[4] CHRU,undefined
来源
Hormones | 2013年 / 12卷
关键词
APECED; IPEX; POEMS; polyendocrine syndrome; thyroid; thyroid autoimmunity;
D O I
暂无
中图分类号
学科分类号
摘要
Even though autoimmune thyroiditis is considered as the most emblematic type of organ-specific autoimmune disorder of autoimmunity, autoimmune thyroid diseases can be associated with other autoimmune endocrine failures or non-endocrine diseases (namely vitiligo, pernicious anemia, myasthenia gravis, autoimmune gastritis, celiac disease, hepatitis). Thyroid disorders, which are the most frequent expression of adult polyendocrine syndrome type 2, occur concomitantly with or secondarily to insulinodependent diabetes, premature ovarian failure, Addison’s disease (Schmidt syndrome, or Carpenter syndrome if associated with diabetes). Testicular failure and hypoparathyroidism are unusual. The disease is polygenic and multifactorial. Disorders of thyroid autoimmunity are, surprisingly, very rare in polyendocrine syndrome type 1 (or APECED) beginning during childhood. They are related to mutations of the AIRE gene that encodes for a transcriptional factor implicated in central and peripheral immune tolerance. Hypothyroidism can also be observed in the very rare IPEX and POEMS syndromes.
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页码:39 / 45
页数:6
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[1]  
Orgiazzi J(2011)The treatment of Graves’ disease: current views and controversies Presse Med 40 1155-1162
[2]  
Carpenter CC(1964)Schmidt’s syndrome (thyroid and adrenal insufficiency). A review of the literature and a report of fifteen new cases including ten instances of coexistent diabetes mellitus Medicine (Baltimore) 43 153-180
[3]  
Solomon N(1980)Autoimmune polyglandular syndromes Pediatr Ann 9 154-162
[4]  
Silverberg SG(2009)Polyglandular autoimmune syndromes Eur J Endocrinol 161 11-20
[5]  
Neufeld M(2012)Polyglandural autoimmune syndrome type 1 Presse Med 41 e651-e662
[6]  
Maclaren N(2010)Autoimmune polyendocrine syndrome type 1 in north-western France: AIRE gene mutation specificities and severe forms needing immunosuppressive therapies Horm Res Paediatr 74 275-284
[7]  
Blizzard R(1956)The syndrome of familial juvenile hypoadrenocorticism, hypoparathyroidism and superficial moniliasis J Clin Endocrinol Metab 16 1374-1387
[8]  
Kahaly GJ(1990)Clinical variation of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy (APECED) in a series of 68 patients N Engl J Med 322 1829-1836
[9]  
Proust-Lemoine E(1994)An autosomal locus causing autoimmune disease: autoimmune polyglandular disease type I assigned to chromosome 21 Nat Genet 8 83-87
[10]  
Sangier-Veber L(2010)Autoantibodies against IL-17A, IL-17F, and IL-22 in patients with chronic mucocutaneous candidiasis and autoimmune polyendocrine syndrome type I J Exp Med 207 291-297