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CTLA4 +49AG(rs231775)和CT60(rs3087243)基因变异与来自墨西哥蒙特雷的墨西哥人群中的斑秃无关。

CTLA4 +49AG (rs231775) and CT60 (rs3087243) gene variants are not associated with alopecia areata in a Mexican population from Monterrey Mexico.

作者信息

Salinas-Santander Mauricio Andrés, Cantu-Salinas Cristina Susana, Ocampo-Candiani Jorge, Suarez-Valencia Victor de Jesus, Ramirez-Guerrero Jennifer Guadalupe, Sanchez-Dominguez Celia Nohemi

机构信息

Department of Investigation, Facultad de Medicina Unidad Saltillo, Universidad Autónoma de Coahuila, Saltillo, Coahuila, Mexico.

Dermatology Service, Hospital Universitario Dr José Eleuterio González, Universidad Autónoma de Nuevo León, Monterrey, Nuevo León, Mexico.

出版信息

An Bras Dermatol. 2020 May-Jun;95(3):283-288. doi: 10.1016/j.abd.2020.03.001. Epub 2020 Mar 20.

Abstract

BACKGROUND

Alopecia areata is an autoimmune disease that produces non-scarring hair loss around the body. Gene variants of the cytotoxic T-lymphocyte antigen 4 (CTLA4) gene, a negative regulator of T-cell response, have been associated with a predisposition to autoimmune diseases in different populations; however, the involvement of these genetic variants in the development of AA is controversial.

OBJECTIVE

The present study evaluated the potential association of two CTLA4 gene variants with alopecia areata in a Mexican population.

METHODS

We genotyped +49AG (rs231775) and CT60 (rs3087243) variants in 50 AA patients and 100 healthy control participants through PCR-RFLP.

RESULTS

No statistical difference was observed for either of the gene variants regarding allele or genotype frequencies between AA patients and the controls when the parameters of family/personal history of autoimmune diseases or gender were considered (p>0.05).

STUDY LIMITATIONS

Small sample size of patients and the data were obtained from Northeast Mexico population.

CONCLUSION

The genetic variants rs231775 and rs3087243 of the CTLA4 gene are not a risk factor for the development of alopecia areata in the analyzed Mexican population.

摘要

背景

斑秃是一种自身免疫性疾病,可导致全身非瘢痕性脱发。细胞毒性T淋巴细胞抗原4(CTLA4)基因作为T细胞反应的负调节因子,其基因变异在不同人群中与自身免疫性疾病的易感性相关;然而,这些基因变异在斑秃发病中的作用仍存在争议。

目的

本研究评估了墨西哥人群中CTLA4基因的两种变异与斑秃的潜在关联。

方法

我们通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)对50例斑秃患者和100名健康对照者的+49AG(rs231775)和CT60(rs3087243)变异进行基因分型。

结果

在考虑自身免疫性疾病家族史/个人史或性别的参数时,斑秃患者与对照组之间在任何一种基因变异的等位基因或基因型频率上均未观察到统计学差异(p>0.05)。

研究局限性

患者样本量小,且数据来自墨西哥东北部人群。

结论

在分析的墨西哥人群中,CTLA4基因的rs231775和rs3087243基因变异不是斑秃发病的危险因素。

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Alopecia areata: A multifactorial autoimmune condition.斑秃:一种多因素自身免疫性疾病。
J Autoimmun. 2019 Mar;98:74-85. doi: 10.1016/j.jaut.2018.12.001. Epub 2018 Dec 15.
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Alopecia areata: a review of disease pathogenesis.斑秃:疾病发病机制的综述。
Br J Dermatol. 2018 Nov;179(5):1033-1048. doi: 10.1111/bjd.16808. Epub 2018 Sep 9.
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CTLA-4: a moving target in immunotherapy.CTLA-4:免疫疗法中的一个移动靶标。
Blood. 2018 Jan 4;131(1):58-67. doi: 10.1182/blood-2017-06-741033. Epub 2017 Nov 8.
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