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埃及患者中谷胱甘肽S-转移酶M1/T1基因多态性与白癜风易感性的相关性研究。

A study of the association of glutathione S-transferase M1/T1 polymorphisms with susceptibility to vitiligo in Egyptian patients.

作者信息

Aly Dalia Gamal, Salem Samar Abdallah, Amr Khalda Sayed, El-Hamid Mahmoud Fawzy Abd

机构信息

Department of Dermatology and Venereology, National Research Centre - Giza, Egypt.

Department of Dermatology, Venereology and Andrology, Ain Shams University - Cairo, Egypt.

出版信息

An Bras Dermatol. 2018 Jan-Feb;93(1):54-58. doi: 10.1590/abd1806-4841.20185796.

Abstract

BACKGROUND

The association of glutathione S-transferases M1/T1 (GSTM1/T1) null polymorphisms with vitiligo was proposed in several studies including two Egyptian studies with contradictory results.

OBJECTIVE

The aim here was to assess the association between GSTM1/T1 null polymorphisms and the susceptibility to vitiligo in a larger sample of Egyptian patients with generalized vitiligo.

METHODS

This study included 122 vitiligo patients and 200 healthy controls that were age, and gender matched. Assessment of GSTM1/T1 gene polymorphisms was done using a multiplex polymerase chain reaction (PCR).

RESULTS

Increased odds of generalized vitiligo was observed with the null genotypes of GSTM1 and GSTT1 polymorphisms (P<0.05). Controls with GSTM1 null/GSTT1+ heterozygosis presented with a 2.97 odds protection from having generalized vitiligo (OR=2.97, 95%CI=1.1-7.7) (P=0.02) compared with patients.

STUDY LIMITATIONS

Small sample size of patients.

CONCLUSIONS

This study showed a significant trend towards an association with the combination of the GSTM1/GSTT1 double null polymorphism and generalized vitiligo. Individuals with GSTM1 null/GSTT1+ heterozygosis have a 2.97 odds protection from having generalized vitiligo compared with patients. It was is the first time, to our knowledge, that such an association has been reported.

摘要

背景

多项研究提出谷胱甘肽S-转移酶M1/T1(GSTM1/T1)基因缺失多态性与白癜风有关,其中包括两项结果相互矛盾的埃及研究。

目的

本研究旨在评估在更大样本的埃及泛发型白癜风患者中,GSTM1/T1基因缺失多态性与白癜风易感性之间的关联。

方法

本研究纳入122例白癜风患者和200例年龄及性别匹配的健康对照。采用多重聚合酶链反应(PCR)对GSTM1/T1基因多态性进行评估。

结果

观察到GSTM1和GSTT1基因多态性的缺失基因型与泛发型白癜风的患病几率增加有关(P<0.05)。与患者相比,GSTM1基因缺失/GSTT1基因正常的杂合子对照患泛发型白癜风的几率有2.97倍的保护作用(OR=2.97,95%CI=1.1-7.7)(P=0.02)。

研究局限性

患者样本量小。

结论

本研究表明,GSTM1/GSTT1双基因缺失多态性与泛发型白癜风之间存在显著关联趋势。与患者相比,GSTM1基因缺失/GSTT1基因正常的杂合子个体患泛发型白癜风的几率有2.97倍的保护作用。据我们所知,这是首次报道这种关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/603b/5871362/8234488a30ae/abd-93-01-0054-g01.jpg

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