Relationship of GSTM1 and GSTT1 genetic variant and markers of oxidative stress and inflammation in smokers with coronary artery disease

Changgao Zhou , Jianjin Tang , Mingwei Wang , Jianjun Yan , Qiming Wang , Jun Zhu , Zhijian Yang , Liansheng Wang
{"title":"Relationship of GSTM1 and GSTT1 genetic variant and markers of oxidative stress and inflammation in smokers with coronary artery disease","authors":"Changgao Zhou ,&nbsp;Jianjin Tang ,&nbsp;Mingwei Wang ,&nbsp;Jianjun Yan ,&nbsp;Qiming Wang ,&nbsp;Jun Zhu ,&nbsp;Zhijian Yang ,&nbsp;Liansheng Wang","doi":"10.1016/S1007-4376(09)60074-5","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><p>To investigate the role of glutathione S-transferase (GST) genetic variants and markers of oxidative stress and inflammation in smoking- related coronary artery disease (CAD) patients.</p></div><div><h3>Methods</h3><p>Five hundred and thirty-five Chinese CAD patients were successfully genotyped. Plasma total antioxidant status (TAOS), glutathione, C-reactive protein (CRP), fibrinogen(FIB) and white blood cell count (WBC) were determined to evaluate the oxidative stress and inflammatory response.</p></div><div><h3>Results</h3><p>GSTM1-0/GSTT1-0 subjects had a higher CRP, FIB, WBC and GSH and a lower TAOS compared to patients with wild-type GSTM1/GSTT1 genes, but there was significant difference only with regards to TAOS. Smokers with the null genotype of GSTT1 had the highest CRP and the lowest TAOS and GSH when compared to the GSTT1-1 genotype with smoking status, or the GSTT1-0 genotype with non-smoking status, or the GSTT1-1 genotype with non-smoking status. However, we found no significant difference between these groups. Also, no significant interaction was observed between genotypes and smoking status in determining CRP levels.</p></div><div><h3>Conclusion</h3><p>Our results suggest that GST polymorphisms do not modify the effect of smoking on markers of oxidative stress and inflammation in Chinese CAD patients.</p></div>","PeriodicalId":100807,"journal":{"name":"Journal of Nanjing Medical University","volume":"23 5","pages":"Pages 300-304"},"PeriodicalIF":0.0000,"publicationDate":"2009-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1007-4376(09)60074-5","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Nanjing Medical University","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1007437609600745","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Objective

To investigate the role of glutathione S-transferase (GST) genetic variants and markers of oxidative stress and inflammation in smoking- related coronary artery disease (CAD) patients.

Methods

Five hundred and thirty-five Chinese CAD patients were successfully genotyped. Plasma total antioxidant status (TAOS), glutathione, C-reactive protein (CRP), fibrinogen(FIB) and white blood cell count (WBC) were determined to evaluate the oxidative stress and inflammatory response.

Results

GSTM1-0/GSTT1-0 subjects had a higher CRP, FIB, WBC and GSH and a lower TAOS compared to patients with wild-type GSTM1/GSTT1 genes, but there was significant difference only with regards to TAOS. Smokers with the null genotype of GSTT1 had the highest CRP and the lowest TAOS and GSH when compared to the GSTT1-1 genotype with smoking status, or the GSTT1-0 genotype with non-smoking status, or the GSTT1-1 genotype with non-smoking status. However, we found no significant difference between these groups. Also, no significant interaction was observed between genotypes and smoking status in determining CRP levels.

Conclusion

Our results suggest that GST polymorphisms do not modify the effect of smoking on markers of oxidative stress and inflammation in Chinese CAD patients.

冠心病吸烟者GSTM1和GSTT1基因变异与氧化应激和炎症标志物的关系
目的探讨谷胱甘肽s -转移酶(GST)基因变异及氧化应激和炎症标志物在吸烟相关性冠心病(CAD)患者中的作用。方法对我国535例冠心病患者进行基因分型。通过测定血浆总抗氧化状态(TAOS)、谷胱甘肽、c反应蛋白(CRP)、纤维蛋白原(FIB)和白细胞计数(WBC)来评估氧化应激和炎症反应。结果GSTM1-0/GSTT1-0基因组与野生型GSTM1/GSTT1基因组相比,CRP、FIB、WBC、GSH升高,TAOS降低,但TAOS差异有统计学意义。GSTT1基因型为零的吸烟者与吸烟的GSTT1-1基因型、不吸烟的GSTT1-0基因型、不吸烟的GSTT1-1基因型相比,CRP最高,TAOS和GSH最低。然而,我们发现这两组之间没有显著差异。此外,基因型和吸烟状况之间在决定CRP水平方面没有明显的相互作用。结论GST多态性不能改变吸烟对冠心病患者氧化应激和炎症标志物的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信