Organ Specificity in Autoimmune Diseases: Thyroid and Islet Autoimmunity in Alopecia Areata

Organ Specificity in Autoimmune Diseases: Thyroid and Islet Autoimmunity in Alopecia Areata
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DOI:
10.1210/jc.2014-3985
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发表时间:
2015-05-01
影响因子:
5.8
通讯作者:
Ikegami, Hiroshi
Ikegami, Hiroshi
中科院分区:
医学2区
文献类型:
--
作者:
Noso, Shinsuke;Park, Choongyong;Ikegami, Hiroshi

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背景:多种自身免疫性疾病,如针对甲状腺和胰岛的自身免疫,经常在单个患者中观察到。虽然斑秃(AA)是最常见的器官特异性自身免疫性疾病之一,但AA与其他自身免疫性疾病的相关性及其遗传基础仍有待分析。目的:探讨AA患者HLA的异同及甲状腺和胰岛自身免疫的临床特点。参与者:新招募的126例AA患者。检测抗胰岛抗体和抗甲状腺抗体,并测定HLA基因型。结果:在与AA相关的自身免疫性疾病中,自身免疫性甲状腺疾病最为常见(10.0%),其次是白癜风(2.7%)和类风湿性关节炎(0.9%),但不包括1型糖尿病(0.0%)。AA患者甲状腺相关自身抗体的患病率明显高于对照组(TSH受体抗体[TRAb]: 42.7% vs 1.2%, P = 1.6 × 10(-46);甲状腺过氧化物酶抗体:29.1% vs 11.6%;P = 1.7 x 10(-6)),而AA患者与对照组之间胰岛相关自身抗体的患病率具有可比性。trab阳性AA患者DRB1*15:01-DQB1*06:02的保护性单倍型频率(12.8%,P = 0.0028,校正P值[P-c] = 0.02)显著高于对照组(4.5%),而trab阴性AA患者DRB1*15:01-DQB1*06:02的频率(7.1%,无统计学意义)显著高于对照组(4.5%)。1型糖尿病易感单倍型DRB1*04:05-DQB1* 04:01的频率(trab阳性:8.5%,trab阴性:11.9%)显著低于1型糖尿病患者(29.5%,P-c = 0.0003, P-c = 0.0008)。结论:AA与甲状腺自身免疫相关,而与胰岛自身免疫无关,其与ⅱ类HLA单倍型对各种自身免疫性疾病的易感或抗性相关。
Context: Multiple autoimmune diseases, such as autoimmunity against the thyroid gland and pancreatic islets, are often observed in a single patient. Although alopecia areata (AA) is one of the most frequent organ-specific autoimmune diseases, the association of AA with other autoimmune diseases and the genetic basis of the association remain to be analyzed.Objective: The aim of this study was to clarify the similarities and differences in HLA and clinical characteristics of thyroid and islet autoimmunity in patients with AA.Participants: A total of 126 patients with AA were newly recruited. Anti-islet and antithyroid autoantibodies were tested, and genotypes of HLA genes were determined.Results: Among the autoimmune diseases associated with AA, autoimmune thyroid disease was most frequent (10.0%), followed by vitiligo (2.7%) and rheumatoid arthritis (0.9%) but not type 1 diabetes (0.0%). The prevalence of thyroid-related autoantibodies in patients with AA was significantly higher than that in controls (TSH receptor antibody [TRAb]: 42.7% vs 1.2%, P = 1.6 x 10(-46); thyroid peroxidase antibody: 29.1% vs 11.6%; P = 1.7 x 10(-6)), whereas the prevalence of islet-related autoantibodies was comparable between patients with AA and control subjects. The frequency of DRB1*15:01-DQB1*06:02, a protective haplotype for type 1 diabetes, was significantly higher in TRAb-positive (12.8%, P = .0028, corrected P value [P-c] = .02) but not TRAb-negative (7.1%, not significant) patients with AA than in control subjects (4.5%). The frequency of DRB1*04:05-DQB1*04: 01, a susceptible haplotype for type 1 diabetes, was significantly lower in patients with AA (TRAb-positive: 8.5%; TRAb-negative: 11.9%) than in those with type 1 diabetes (29.5%, P-c = .0003 and P-c = .0008, respectively).Conclusion: AA was associated with thyroid autoimmunity but not islet autoimmunity, which correlated with class II HLA haplotypes susceptible or resistant to each autoimmune disease.