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非节段性白癜风中甲状腺自身免疫与HLA - DRB1和HLA - DQB1多态性的关系:一项横断面研究。

Thyroid autoimmunity in relation to HLA-DRB1 and HLA-DQB1 polymorphism in nonsegmental vitiligo: a cross-sectional-study.

作者信息

Bouayad Abdellatif, Benzekri Laila

机构信息

Faculty of Medicine and Pharmacy, Mohammed First University Oujda, Morocco.

Department of Dermatology, Faculty of Medicine and Pharmacy, Mohammed V Souissi University, Ibn Sina Hospital Rabat, Morocco.

出版信息

Am J Transl Res. 2024 Feb 15;16(2):524-530. doi: 10.62347/LDYE8203. eCollection 2024.

Abstract

OBJECTIVES

Nonsegmental vitiligo (NSV) is frequently associated with thyroid autoimmunity (TAI), however, the immunopathogenic mechanisms of such association remain to be investigated. The aims of this work were to estimate the frequency of TAI and to describe the genetic polymorphism in the human leukocyte antigen (HLA)-DRB1 and -DQB1 loci in TAI susceptibility among patients with NSV.

PATIENTS AND METHODS

In this cross-sectional study, screening for TAI was performed in 97 Moroccan patients with NSV by measuring antibodies against thyroid peroxidase (TPOAb) and thyroglobulin (TGAb). HLA-DRB1 and -DQB1 were determined with single specific primer-polymerase chain reaction (PCR-SSP) typing methods.

RESULTS

TAI was diagnosed in 20 patients with NSV (20.6%). The phenotypic frequency of DQB105 (OR = 5.04; P = 0.006; pc = 0.036) was significantly higher in NSV patients with TAI. Genotype DQB105/DQB106 (OR = 25.33; P = 0.001; pc = 0.003) confer susceptibility to TAI in NSV patients. NSV patients with TAI and early onset vitiligo have an extremely high phenotype frequency of DQB105 allele (OR = 14.67; P = 0.001; pc = 0.048) and DQB105/DQB106 genotype (OR = 26.55; P = 0.01; pc = 0.03). TAI in patients with NSV was (6.2%) associated with onset of clinical thyroid disease based on TSH and free T4.

CONCLUSION

Our findings suggest that HLA-DQ polymorphisms influence TAI risk in subjects with NSV, although HLA does not completely explain the co-occurrence of these two diseases.

摘要

目的

非节段性白癜风(NSV)常与甲状腺自身免疫(TAI)相关,然而,这种关联的免疫致病机制仍有待研究。本研究的目的是评估TAI的发生率,并描述NSV患者中人类白细胞抗原(HLA)-DRB1和-DQB1基因座在TAI易感性方面的基因多态性。

患者与方法

在这项横断面研究中,通过检测抗甲状腺过氧化物酶(TPOAb)和甲状腺球蛋白(TGAb)抗体,对97例摩洛哥NSV患者进行了TAI筛查。采用单特异性引物聚合酶链反应(PCR-SSP)分型方法测定HLA-DRB1和-DQB1。

结果

97例NSV患者中,20例(20.6%)被诊断为TAI。DQB105的表型频率在合并TAI的NSV患者中显著更高(OR = 5.04;P = 0.006;pc = 0.036)。基因型DQB105/DQB106(OR = 25.33;P = 0.001;pc = 0.003)使NSV患者易患TAI。合并TAI且白癜风发病早的NSV患者DQB105等位基因(OR = 14.67;P = 0.001;pc = 0.048)和DQB105/DQB106基因型(OR = 26.55;P = 0.01;pc = 0.03)的表型频率极高。基于促甲状腺激素(TSH)和游离甲状腺素(FT4),NSV患者中的TAI与临床甲状腺疾病的发生相关(6.2%)。

结论

我们的研究结果表明,HLA-DQ多态性影响NSV患者患TAI的风险,尽管HLA不能完全解释这两种疾病的同时发生。

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