• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

将健康问题归因于含有机磷酸盐的羊药浴液的农民体内谷胱甘肽S-转移酶、细胞色素P450和对氧磷酶1基因多态性

GST CYP and PON1 polymorphisms in farmers attributing ill health to organophosphate-containing sheep dip.

作者信息

Povey A C, Jury F, Dippnall W M, Smith A E, Thomson S, Mackness B, Mackness M, Durrington P, Cherry N M

机构信息

Centre for Occupational and Environmental Health, University of Manchester, UK.

出版信息

Biomarkers. 2007 Mar-Apr;12(2):188-202. doi: 10.1080/13547500601043500.

DOI:10.1080/13547500601043500
PMID:17536768
Abstract

Previously we reported that in sheep dippers exposed to organophosphates the frequency of paraoxonase (PON1) polymorphisms differed between those with or without self-reported ill health. We have now examined whether polymorphisms in other genes involved in xenobiotic metabolism alter disease risk in this population. There were elevated but non-significant risks associated with the CYP2D6 WT genotype (odds ratio (OR) 1.47, 95% CI 0.83-2.60), or a GSTP1B or C allele (OR 1.37, 95% CI 0.88-2.01) or being GSTM12/GSTT12 homozygous (OR 1.61, 95% CI 0.74-3.48). Similar results were generally obtained after the exclusion of subjects to obtain a more homogenous case-referent population: for double null GSTM1 and GSTT1 homozygotes the OR was 2.06 (95% CI 0.85-2.04). In those also likely to have been exposed to diazinon, risks associated with a GSTP1B or C allele (OR 1.82, 95% CI 0.92-3.63) or a GSTM12/GSTT12 homozygous (OR 2.60, 95% CI 0.72-10.42) were elevated but not to a significant extent. Risk associated with PON1 genotype and phenotype varied with CYP2D6 and GSTP1 genotype but not consistently with a priori hypotheses. Further work is necessary to delineate more clearly pathways of organophosphate activation and non-PON1 pathways of detoxification and to confirm whether CYP and GST polymorphisms alter disease risk in populations exposed to organophosphates.

摘要

此前我们报道,在接触有机磷的牧羊人中,对氧磷酶(PON1)基因多态性的频率在有或无自我报告健康问题的人群中存在差异。我们现在研究了参与异生物质代谢的其他基因的多态性是否会改变该人群的疾病风险。CYP2D6野生型基因型(比值比(OR)为1.47,95%置信区间为0.83 - 2.60)、GSTP1B或C等位基因(OR为1.37,95%置信区间为0.88 - 2.01)或GSTM12/GSTT12纯合子(OR为1.61,95%置信区间为0.74 - 3.48)与疾病风险升高相关,但差异无统计学意义。在排除部分受试者以获得更同质的病例对照人群后,通常得到了类似结果:对于GSTM1和GSTT1双缺失纯合子,OR为2.06(95%置信区间为0.85 - 2.04)。在那些可能也接触过二嗪农的人群中,GSTP1B或C等位基因(OR为1.82,95%置信区间为0.92 - 3.63)或GSTM12/GSTT12纯合子(OR为2.60,95%置信区间为0.72 - 10.42)与疾病风险升高相关,但升高幅度不显著。与PON1基因型和表型相关的风险随CYP2D6和GSTP1基因型而变化,但并不始终符合先验假设。有必要进一步开展工作,以更清楚地描绘有机磷激活途径和非PON1解毒途径,并确认CYP和GST多态性是否会改变接触有机磷人群的疾病风险。

相似文献

1
GST CYP and PON1 polymorphisms in farmers attributing ill health to organophosphate-containing sheep dip.将健康问题归因于含有机磷酸盐的羊药浴液的农民体内谷胱甘肽S-转移酶、细胞色素P450和对氧磷酶1基因多态性
Biomarkers. 2007 Mar-Apr;12(2):188-202. doi: 10.1080/13547500601043500.
2
Association of genetic polymorphism of glutathione S-transferase (GSTM1, GSTT1, GSTP1) with bladder cancer susceptibility.谷胱甘肽 S-转移酶 (GSTM1、GSTT1、GSTP1) 基因多态性与膀胱癌易感性的关系。
Urol Oncol. 2013 Oct;31(7):1193-203. doi: 10.1016/j.urolonc.2011.11.027. Epub 2011 Dec 11.
3
Gene-environmental interactions and organophosphate toxicity.基因-环境相互作用与有机磷毒性。
Toxicology. 2010 Dec 30;278(3):294-304. doi: 10.1016/j.tox.2010.02.007. Epub 2010 Feb 13.
4
Glutathione S-transferase gene polymorphisms (GSTM1, GSTT1, GSTP1) and prostate cancer: a case-control study in Tehran, Iran.谷胱甘肽 S-转移酶基因多态性(GSTM1、GSTT1、GSTP1)与前列腺癌:伊朗德黑兰的病例对照研究。
Prostate Cancer Prostatic Dis. 2011 Jun;14(2):105-13. doi: 10.1038/pcan.2010.54. Epub 2011 Jan 18.
5
GSTA1, GSTM1, GSTP1, and GSTT1 polymorphisms and susceptibility to smoking-related bladder cancer: a case-control study.谷胱甘肽 S-转移酶 A1、M1、P1 和 T1 多态性与吸烟相关膀胱癌易感性的关系:一项病例对照研究。
Urol Oncol. 2013 Oct;31(7):1184-92. doi: 10.1016/j.urolonc.2011.08.005.
6
Paraoxonase polymorphisms and self-reported chronic ill-health in farmers dipping sheep.农民给羊浸洗时对氧磷酶基因多态性与自我报告的慢性健康问题
Occup Med (Lond). 2005 Jun;55(4):282-6. doi: 10.1093/occmed/kqi128.
7
The role of PON1 and CYP2D6 genes in susceptibility to organophosphorus chronic intoxication in Egyptian patients.PON1和CYP2D6基因在埃及患者对有机磷慢性中毒易感性中的作用。
Neurotoxicology. 2016 Mar;53:102-107. doi: 10.1016/j.neuro.2015.12.015. Epub 2015 Dec 23.
8
Association between polymorphism of GSTP1, GSTT1, GSTM1 and CYP2E1 genes and susceptibility to benzene-induced hematotoxicity.GSTP1、GSTT1、GSTM1 和 CYP2E1 基因多态性与苯致血液毒性易感性的关系。
Arch Toxicol. 2018 Jun;92(6):1983-1990. doi: 10.1007/s00204-017-2104-9. Epub 2017 Dec 4.
9
Genetic polymorphisms in GSTM1, GSTT1, GSTP1, GSTM3 and the susceptibility to gallbladder cancer in North India.谷胱甘肽S-转移酶M1、谷胱甘肽S-转移酶T1、谷胱甘肽S-转移酶P1、谷胱甘肽S-转移酶M3基因多态性与印度北部胆囊癌易感性
Biomarkers. 2006 May-Jun;11(3):250-61. doi: 10.1080/13547500600648697.
10
Paraoxonase (PON1) polymorphisms in farmers attributing ill health to sheep dip.将健康问题归因于羊药浴的农民体内对氧磷酶(PON1)基因多态性
Lancet. 2002 Mar 2;359(9308):763-4. doi: 10.1016/s0140-6736(02)07847-9.

引用本文的文献

1
Paraoxonase 1 (PON1) as a genetic determinant of susceptibility to organophosphate toxicity.对氧磷酶 1(PON1)作为有机磷毒性易感性的遗传决定因素。
Toxicology. 2013 May 10;307:115-22. doi: 10.1016/j.tox.2012.07.011. Epub 2012 Jul 31.
2
Allele and genotype frequencies of CYP2B6 and CYP2C19 polymorphisms in Egyptian agricultural workers.埃及农业工人 CYP2B6 和 CYP2C19 多态性的等位基因和基因型频率。
J Toxicol Environ Health A. 2012;75(4):232-41. doi: 10.1080/15287394.2012.641201.
3
Experimental strategy for translational studies of organophosphorus pesticide neurotoxicity based on real-world occupational exposures to chlorpyrifos.
基于现实职业性接触毒死蜱的有机磷农药神经毒性转化研究的实验策略。
Neurotoxicology. 2012 Aug;33(4):660-8. doi: 10.1016/j.neuro.2011.12.017. Epub 2012 Jan 4.
4
Correlating neurobehavioral performance with biomarkers of organophosphorous pesticide exposure.将神经行为表现与有机磷农药接触的生物标志物相关联。
Neurotoxicology. 2011 Mar;32(2):268-76. doi: 10.1016/j.neuro.2010.12.008. Epub 2010 Dec 21.