[乙醇代谢酶基因多态性对饮酒行为的影响]

Joo Young Kee, Min Ok Kim, Il Young You, Ji Young Chai, Eui Sil Hong, Sung Chul An, Heon Kim, Seon Mee Park, Sei Jin Youn, Hee Bok Chae
{"title":"[乙醇代谢酶基因多态性对饮酒行为的影响]","authors":"Joo Young Kee,&nbsp;Min Ok Kim,&nbsp;Il Young You,&nbsp;Ji Young Chai,&nbsp;Eui Sil Hong,&nbsp;Sung Chul An,&nbsp;Heon Kim,&nbsp;Seon Mee Park,&nbsp;Sei Jin Youn,&nbsp;Hee Bok Chae","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Background/aims: </strong>Genetic variations of ethanol-metabolizing enzymes can affect alcohol drinking behavior. The aims of this study were to investigate and compare the distributions of these genetic polymorphisms between a healthy control group and a heavy drinker group which included an alcoholic liver cirrhosis group.</p><p><strong>Methods: </strong>Genotypes of ADH2, ALDH2, CYP2E1, and catalase were identified by polymerase chain reaction and restriction fragment length polymorphism. Genomic DNA was extracted from peripheral leukocytes in 42 healthy controls, 12 heavy drinkers, and 30 alcoholic liver cirrhosis patients.</p><p><strong>Results: </strong>1) The genotype frequencies of ALDH2 (1*1), ADH2 (1*1), CYP2E1 (c1c1), and catalase1 (TT) were 69%, 55%, 38%, and 12%, respectively in healthy Korean males. 2) There was a significant difference in the distribution of the genetic polymorphism of ALDH2 between the control group and heavy drinker group (12 heavy drinkers and 30 alcoholic liver cirrhosis patients). The genotype frequency of ALDH2 mutant, ALDH2 (1*2) and ALDH2 (2*2) in the heavy drinker group (12%) was significantly lower than that in the control group (30%). 3) We didn't find anyone with ALDH2 homozygote mutant (DD) in the heavy drinker group. 4) There was no significant difference in the distribution of genetic polymorphisms in ADH2, CYP2E1 and catalase1 between the two groups.</p><p><strong>Conclusions: </strong>These results suggest that the absence of ALDH2 mutant genotype is strongly related to heavy drinking behavior. We can not prove, however, any evidence that the polymorphisms of other ethanol-metabolizing enzymes are associated with the determination of alcohol-drinking behavior.</p>","PeriodicalId":85610,"journal":{"name":"Taehan Kan Hakhoe chi = The Korean journal of hepatology","volume":"9 2","pages":"89-97"},"PeriodicalIF":0.0000,"publicationDate":"2003-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Effects of genetic polymorphisms of ethanol-metabolizing enzymes on alcohol drinking behaviors].\",\"authors\":\"Joo Young Kee,&nbsp;Min Ok Kim,&nbsp;Il Young You,&nbsp;Ji Young Chai,&nbsp;Eui Sil Hong,&nbsp;Sung Chul An,&nbsp;Heon Kim,&nbsp;Seon Mee Park,&nbsp;Sei Jin Youn,&nbsp;Hee Bok Chae\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background/aims: </strong>Genetic variations of ethanol-metabolizing enzymes can affect alcohol drinking behavior. The aims of this study were to investigate and compare the distributions of these genetic polymorphisms between a healthy control group and a heavy drinker group which included an alcoholic liver cirrhosis group.</p><p><strong>Methods: </strong>Genotypes of ADH2, ALDH2, CYP2E1, and catalase were identified by polymerase chain reaction and restriction fragment length polymorphism. Genomic DNA was extracted from peripheral leukocytes in 42 healthy controls, 12 heavy drinkers, and 30 alcoholic liver cirrhosis patients.</p><p><strong>Results: </strong>1) The genotype frequencies of ALDH2 (1*1), ADH2 (1*1), CYP2E1 (c1c1), and catalase1 (TT) were 69%, 55%, 38%, and 12%, respectively in healthy Korean males. 2) There was a significant difference in the distribution of the genetic polymorphism of ALDH2 between the control group and heavy drinker group (12 heavy drinkers and 30 alcoholic liver cirrhosis patients). The genotype frequency of ALDH2 mutant, ALDH2 (1*2) and ALDH2 (2*2) in the heavy drinker group (12%) was significantly lower than that in the control group (30%). 3) We didn't find anyone with ALDH2 homozygote mutant (DD) in the heavy drinker group. 4) There was no significant difference in the distribution of genetic polymorphisms in ADH2, CYP2E1 and catalase1 between the two groups.</p><p><strong>Conclusions: </strong>These results suggest that the absence of ALDH2 mutant genotype is strongly related to heavy drinking behavior. We can not prove, however, any evidence that the polymorphisms of other ethanol-metabolizing enzymes are associated with the determination of alcohol-drinking behavior.</p>\",\"PeriodicalId\":85610,\"journal\":{\"name\":\"Taehan Kan Hakhoe chi = The Korean journal of hepatology\",\"volume\":\"9 2\",\"pages\":\"89-97\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2003-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Taehan Kan Hakhoe chi = The Korean journal of hepatology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Taehan Kan Hakhoe chi = The Korean journal of hepatology","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

背景/目的:乙醇代谢酶的遗传变异可影响饮酒行为。本研究的目的是调查和比较这些基因多态性在健康对照组和重度饮酒者组(包括酒精性肝硬化组)之间的分布。方法:采用聚合酶链反应和限制性片段长度多态性方法对ADH2、ALDH2、CYP2E1和过氧化氢酶进行基因型鉴定。从42名健康对照者、12名重度饮酒者和30名酒精性肝硬化患者的外周血白细胞中提取基因组DNA。结果:1)韩国健康男性ALDH2(1*1)、ADH2(1*1)、CYP2E1 (c1c1)、过氧化氢酶1 (TT)基因型频率分别为69%、55%、38%、12%。2) ALDH2基因多态性在对照组和重度饮酒者组(12例重度饮酒者和30例酒精性肝硬化患者)之间的分布有显著差异。重度饮酒组ALDH2突变体、ALDH2(1*2)和ALDH2(2*2)基因型频率(12%)显著低于对照组(30%)。3)重度饮酒者中未发现ALDH2纯合子突变体(DD)。4) ADH2、CYP2E1和过氧化氢酶1基因多态性在两组间的分布无显著差异。结论:这些结果表明ALDH2突变基因型的缺失与酗酒行为密切相关。然而,我们不能证明任何证据表明其他乙醇代谢酶的多态性与饮酒行为的决定有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
[Effects of genetic polymorphisms of ethanol-metabolizing enzymes on alcohol drinking behaviors].

Background/aims: Genetic variations of ethanol-metabolizing enzymes can affect alcohol drinking behavior. The aims of this study were to investigate and compare the distributions of these genetic polymorphisms between a healthy control group and a heavy drinker group which included an alcoholic liver cirrhosis group.

Methods: Genotypes of ADH2, ALDH2, CYP2E1, and catalase were identified by polymerase chain reaction and restriction fragment length polymorphism. Genomic DNA was extracted from peripheral leukocytes in 42 healthy controls, 12 heavy drinkers, and 30 alcoholic liver cirrhosis patients.

Results: 1) The genotype frequencies of ALDH2 (1*1), ADH2 (1*1), CYP2E1 (c1c1), and catalase1 (TT) were 69%, 55%, 38%, and 12%, respectively in healthy Korean males. 2) There was a significant difference in the distribution of the genetic polymorphism of ALDH2 between the control group and heavy drinker group (12 heavy drinkers and 30 alcoholic liver cirrhosis patients). The genotype frequency of ALDH2 mutant, ALDH2 (1*2) and ALDH2 (2*2) in the heavy drinker group (12%) was significantly lower than that in the control group (30%). 3) We didn't find anyone with ALDH2 homozygote mutant (DD) in the heavy drinker group. 4) There was no significant difference in the distribution of genetic polymorphisms in ADH2, CYP2E1 and catalase1 between the two groups.

Conclusions: These results suggest that the absence of ALDH2 mutant genotype is strongly related to heavy drinking behavior. We can not prove, however, any evidence that the polymorphisms of other ethanol-metabolizing enzymes are associated with the determination of alcohol-drinking behavior.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
[The significance of urine sodium measurement after furosemide administration in diuretics-unresponsive patients with liver cirrhosis]. [A case of toxic hepatitis induced by habitual glue sniffing]. New antiviral therapies for hepatitis C. [Recent changes of organism and treatment in pyogenic liver abscess]. [Serum ALT and HBV DNA levels in patients with HBeAg-negative chronic hepatitis B].
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1