Suppr超能文献

砷代谢基因多态性与中国西北地区高剂量无机砷暴露人群砷致皮肤损伤的关系。

Association between arsenic metabolism gene polymorphisms and arsenic-induced skin lesions in individuals exposed to high-dose inorganic arsenic in northwest China.

机构信息

Center for Endemic Disease Control, Chinese Center for Disease Control and Prevention, Harbin Medical University; Key Lab of Etiology and Epidemiology, Education Bureau of Hei Long Jiang Province & Ministry of Health, Harbin, 150081, China.

Dongcheng Haidian District Center for Disease Control and Prevention, Beijing, 100009, China.

出版信息

Sci Rep. 2018 Jan 11;8(1):413. doi: 10.1038/s41598-017-18925-3.

Abstract

Individuals in a given environment contaminated with arsenic have different susceptibilities to disease, which may be related to arsenic metabolism, age, gender, genetics and other factors. This study recruited 850 subjects, including 331 cases and 519 controls, from populations exposed to high levels of arsenic in drinking water in northwest China. Genotypes were determined using a custom-by-design 48-Plex SNPscan kit. The results indicated that subjects who carried at least one C allele for GSTO1 rs11191979 polymorphism, at least one A allele for GSTO1 rs2164624, at least one A allele for GSTO1 rs4925, the AG genotype for GSTO2 rs156697, the AG genotype or at least one G allele for GSTO2 rs2297235 or the GG genotype or at least one G allele for PNP rs3790064 had an increased risk of arsenic-related skin lesions. In addition, the haplotype CT between rs4925 and rs11191979 appeared to confer a high risk of arsenic-included skin lesions (OR = 1.377, 95% CI = 1.03-1.84), as did the haplotype GCG among rs156697, rs157077 and rs2297235 (OR = 2.197, 95% CI = 1.08-4.44). The results showed that the variants of GSTO1, GSTO2 and PNP render the susceptible toward developing arsenic-induced skin lesions in individuals exposed to high-dose inorganic arsenic in northwest China.

摘要

在受砷污染的特定环境中,个体对疾病的易感性不同,这可能与砷代谢、年龄、性别、遗传等因素有关。本研究在中国西北地区饮用水砷暴露人群中招募了 850 名受试者,包括 331 例病例和 519 例对照。采用定制设计的 48 plex SNPscan 试剂盒确定基因型。结果表明,GSTO1 rs11191979 多态性至少携带一个 C 等位基因、GSTO1 rs2164624 至少携带一个 A 等位基因、GSTO1 rs4925 至少携带一个 A 等位基因、GSTO2 rs156697 的 AG 基因型、GSTO2 rs2297235 至少携带一个 G 等位基因或 AG 基因型或至少携带一个 G 等位基因、PNP rs3790064 的 GG 基因型或至少携带一个 G 等位基因的个体发生砷相关性皮肤损伤的风险增加。此外,rs4925 和 rs11191979 之间的 CT 单体型似乎赋予砷相关皮肤损伤的高风险(OR=1.377,95%CI=1.03-1.84),rs156697、rs157077 和 rs2297235 之间的 GCG 单体型也是如此(OR=2.197,95%CI=1.08-4.44)。结果表明,GSTO1、GSTO2 和 PNP 的变异使中国西北地区高剂量无机砷暴露个体易发生砷诱导的皮肤损伤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9372/5765042/9120d1e7a1bb/41598_2017_18925_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验