高级检索
当前位置: 首页 > 详情页

Association of glutathione S-transferase M1/T1 polymorphisms with susceptibility to vitiligo

文献详情

资源类型:
WOS体系:
Pubmed体系:

收录情况: ◇ SCIE

机构: [1]Department of Physiology, School of Basic Medical Sciences, Kunming Medical University, Kunming, Yunnan, China [2]Department of Dermatology, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China [3]Division of Science and Technology, Kunming Medical University, Kunming, Yunnan, China
出处:
ISSN:

关键词: Vitiligo Polymorphism Glutathione S-transferases M1 Glutathione S-transferases T1 Meta-analysis

摘要:
Background: Some studies suggested that Glutathione S-transferases M1/F1(GSTM1/F1) null polymorphisms may be associated with the risk of vitiligo. Aims: The purpose of this study is to further evaluate the association between GSTM1/T1 null polymorphisms and the susceptibility to vitiligo. Methods: We carried out a retrieval of studies in the databases. Odds ratios (OR) and 95% confidence intervals (95% CIs) were used to assess the strength of this association. We analyzed the data using Stata 11.0. Results: Six case-control studies including 1358 cases and 1673 controls were included in this meta-analysis. Our overall results showed the GSTM1 or GSTT1 null polymorphism was associated with vitiligo (GSTM1:OR = 1.59, 95% CI: 1.21-2.08, P = 0.001; GSTT1: OR = 1.30, 95% CI: 1.12-1.51,P = 0.001). In the subgroup analysis, the GSTM1 null polymorphism might be a genetic risk factor to vitiligo in East Asian (OR = 1.71, 95% CI: 1.12-2.63, P = 0.014) but not in the Mediterranean, however individuals with the GSTT1 null polymorphism in the Mediterranean (OR = 1.76, 95% CI: 1.15-2.71, P = 0.010) but not in East Asian have a greater predisposition to vitiligo. In addition there was also a significant trend toward an association with the combination of the GSTM1 null and GSTT1 null in either East Asians or Mediterraneans. Conclusion: The GSTM1/T1 null polymorphisms may be associated with vitiligo. More studies are needed to confirm this conclusion. (C) 2013 Elsevier B.V. All rights reserved.

基金:
语种:
被引次数:
WOS:
PubmedID:
中科院(CAS)分区:
出版当年[2014]版:
大类 | 4 区 生物
小类 | 4 区 遗传学
最新[2025]版:
大类 | 3 区 生物学
小类 | 3 区 遗传学
JCR分区:
出版当年[2013]版:
Q3 GENETICS & HEREDITY
最新[2023]版:
Q2 GENETICS & HEREDITY

影响因子: 最新[2023版] 最新五年平均 出版当年[2013版] 出版当年五年平均 出版前一年[2012版] 出版后一年[2014版]

第一作者:
第一作者机构: [1]Department of Physiology, School of Basic Medical Sciences, Kunming Medical University, Kunming, Yunnan, China
共同第一作者:
通讯作者:
通讯机构: [2]Department of Dermatology, First Affiliated Hospital of Kunming Medical University, Kunming, Yunnan, China [3]Division of Science and Technology, Kunming Medical University, Kunming, Yunnan, China [*1]295 Xichang Road, Kunming 650032, Yunnan, China [*2]1168 West Chunrong Road, Yuhua Avenue, Chenggong District, Kunming 650500, Yunnan, China.
推荐引用方式(GB/T 7714):
APA:
MLA:

资源点击量:88108 今日访问量:0 总访问量:732 更新日期:2025-04-01 建议使用谷歌、火狐浏览器 常见问题

版权所有©2020 云南省第一人民医院 技术支持:重庆聚合科技有限公司 地址:云南省昆明市西山区金碧路157号