Association of SOD1 rs36232792 with opioid use disorder and a novel PCR-RFLP method for SOD2 rs5746136.

IF 1.9 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Seval Küçükparmaksız, Dilek Kaya Akyüzlü, Selin Özkan Kotiloğlu, Mustafa Danışman
{"title":"Association of <i>SOD1</i> rs36232792 with opioid use disorder and a novel PCR-RFLP method for <i>SOD2</i> rs5746136.","authors":"Seval Küçükparmaksız, Dilek Kaya Akyüzlü, Selin Özkan Kotiloğlu, Mustafa Danışman","doi":"10.1080/14622416.2025.2490467","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>The aim of this study is to find out the effect of <i>SOD1</i> rs36232792 and <i>SOD2</i> rs5746136 on the risk of opioid use disorder (OUD).</p><p><strong>Methods: </strong>Individuals with OUD (<i>n</i> = 101) and controls (<i>n</i> = 104) were included. <i>SOD1</i> rs36232792 was genotyped by PCR. A novel PCR-RFLP method for <i>SOD2</i> rs5746136 was optimized.</p><p><strong>Results: </strong>A significant difference was observed between individuals with OUD and controls in view of the frequency of 'Ins/Del+Del/Del' genotypes of the <i>SOD1</i> rs36232792 (<i>p</i> = 0.049), but not for <i>SOD2</i> rs5746136 (<i>p</i> = 0.254). The intensity of anxiety and depressive symptoms was significantly higher in individuals with OUD compared to controls (<i>p</i> = 0.001).</p><p><strong>Conclusion: </strong>The <i>SOD1</i> rs36232792 polymorphism could contribute to the risk of OUD in a Turkish population. A novel PCR-RFLP method for <i>SOD2</i> rs5746136 confirmed by sequencing can be used in a research laboratory without advanced equipment.</p>","PeriodicalId":20018,"journal":{"name":"Pharmacogenomics","volume":" ","pages":"1-11"},"PeriodicalIF":1.9000,"publicationDate":"2025-04-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pharmacogenomics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1080/14622416.2025.2490467","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Aim: The aim of this study is to find out the effect of SOD1 rs36232792 and SOD2 rs5746136 on the risk of opioid use disorder (OUD).

Methods: Individuals with OUD (n = 101) and controls (n = 104) were included. SOD1 rs36232792 was genotyped by PCR. A novel PCR-RFLP method for SOD2 rs5746136 was optimized.

Results: A significant difference was observed between individuals with OUD and controls in view of the frequency of 'Ins/Del+Del/Del' genotypes of the SOD1 rs36232792 (p = 0.049), but not for SOD2 rs5746136 (p = 0.254). The intensity of anxiety and depressive symptoms was significantly higher in individuals with OUD compared to controls (p = 0.001).

Conclusion: The SOD1 rs36232792 polymorphism could contribute to the risk of OUD in a Turkish population. A novel PCR-RFLP method for SOD2 rs5746136 confirmed by sequencing can be used in a research laboratory without advanced equipment.

SOD1 rs36232792与阿片类药物使用障碍的关联及SOD2 rss5746136的新型PCR-RFLP方法
目的:本研究旨在探讨SOD1 rs36232792和SOD2 rss5746136对阿片类药物使用障碍(OUD)风险的影响。方法:纳入OUD患者(n = 101)和对照组(n = 104)。用PCR方法对SOD1 rs36232792进行基因分型。优化了SOD2 rs5746136的PCR-RFLP检测方法。结果:在SOD1 rs36232792的“Ins/Del+Del/Del”基因型频率上,OUD个体与对照组有显著差异(p = 0.049),而SOD2 rss5746136无显著差异(p = 0.254)。与对照组相比,OUD患者的焦虑和抑郁症状强度显著升高(p = 0.001)。结论:SOD1 rs36232792多态性可能与土耳其人群的OUD风险有关。经测序确认的新型SOD2 rs5746136 PCR-RFLP方法可以在没有先进设备的研究实验室中使用。
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
Pharmacogenomics
Pharmacogenomics 医学-药学
CiteScore
3.40
自引率
9.50%
发文量
88
审稿时长
4-8 weeks
期刊介绍: Pharmacogenomics (ISSN 1462-2416) is a peer-reviewed journal presenting reviews and reports by the researchers and decision-makers closely involved in this rapidly developing area. Key objectives are to provide the community with an essential resource for keeping abreast of the latest developments in all areas of this exciting field. Pharmacogenomics is the leading source of commentary and analysis, bringing you the highest quality expert analyses from corporate and academic opinion leaders in the field.
×
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