Two cases of autoimmune polyendocrine syndrome type Ⅰ caused by AIRE gene mutation
10.3760/cma.j.issn.1000-6699.2019.12.005
- VernacularTitle: AIRE基因突变致自身免疫性多内分泌腺病综合征Ⅰ型两例分析
- Author:
Qin LONG
1
;
Qing ZHANG
;
Youbo YANG
;
Xiaodan LONG
;
Zhaohui MO
;
Ping JIN
Author Information
1. Department of Endorcrinology, the Third Xiangya Hospital, Central South University, Changsha 410007, China
- Publication Type:Journal Article
- Keywords:
Autoimmune polyendocrine syndrome type Ⅰ;
AIRE gene;
Mutation
- From:
Chinese Journal of Endocrinology and Metabolism
2019;35(12):1019-1024
- CountryChina
- Language:Chinese
-
Abstract:
Objective:Autoimmune polyendocrine syndrome type Ⅰ(APS-Ⅰ) is caused by mutations in the autoimmune regulator gene (AIRE) gene. In this study, phenotype and AIRE gene analysis were performed in two patients with APS-Ⅰ.
Methods:Peripheral blood samples were collected from two patients with APS-Ⅰ and their families. All exons of the AIRE gene and adjacent exon-intron sequences were amplified by PCR and subsequently sequenced. The silico analysis was performed to predict the possible impact of the mutations on the function of the AIRE protein. At the same time, 100 healthy controls were selected to confirm the mutation.
Results:Case 1 was a 31-year-old female who exhibited chronic mucocutaneous candidiasis, hypoparathyroidism, Addison′s disease, Hashimoto′s thyroiditis, and premature ovarian failure. A homozygous c. 483_484insC mutation in exon 4 of AIRE gene was identified in this patient. Her parents, siblings and son were heterozygous for this mutation, which is consistent with the autosomal recessive inheritance pattern. Case 2 was a 34-year-old male who had mucocutaneous candidiasis, Addison′s disease, primary hypoparathyroidism, and Hashimoto′s thyroiditis. A compound heterozygous AIRE mutation (c.179A>G/C.463+ 2T>C) were identified in this patient. His father was heterozygous for c. 179A>G mutation, and his mother was heterozygous for C. 463+ 2T>C, which is consistent with autosomal recessive inheritance mode. The c. 483_484insC and c. 463+ 2T>C have been reported to be pathogenic. The c. 179A>G mutation was predicted pathogenic by SIFT and PolyPhen2 software, which was not detected in 100 healthy controls. It has not been reported in the HGDM database and is a novel mutation.
Conclusion:We identified a novel AIRE gene mutation (c.179A>G), which contributed to further understanding of the pathogenesis of APS-Ⅰ. The clinical variation and rarity of APS-Ⅰ makes the syndrome hard to recognize. Early recognition of symptoms and screening for AIRE mutation in patients with APS-Ⅰ has important clinical implications for the diagnosis and treatment.
