The Predisposition for Type 2 Diabetes Mellitus and Metabolic Syndrome.

IF 0.5 4区 医学 Q4 GENETICS & HEREDITY
C Zenoaga-Barbăroșie, L Berca, T Vassu-Dimov, M Toma, M I Nica, O A Alexiu-Toma, C Ciornei, A Albu, S Nica, C Nistor, R Nica
{"title":"The Predisposition for Type 2 Diabetes Mellitus and Metabolic Syndrome.","authors":"C Zenoaga-Barbăroșie,&nbsp;L Berca,&nbsp;T Vassu-Dimov,&nbsp;M Toma,&nbsp;M I Nica,&nbsp;O A Alexiu-Toma,&nbsp;C Ciornei,&nbsp;A Albu,&nbsp;S Nica,&nbsp;C Nistor,&nbsp;R Nica","doi":"10.2478/bjmg-2023-0003","DOIUrl":null,"url":null,"abstract":"<p><p>Type 2 diabetes mellitus (T2DM) and metabolic syndrome (MetS) are diseases caused by the interaction of genetic and non-genetic factors. Therefore, the aim of our study was to investigate the association between six common genetic polymorphisms and T2DM and MetS in males. A total of 120 T2DM, 75 MetS, and 120 healthy controls (HC) were included in the study. <i>ACE</i> ID, <i>eNOS</i> 4a/b, <i>ATR1</i> A1166C, <i>OXTR</i> (A>G), <i>SOD1</i> +35A/C, <i>CAT</i>-21A/T gene polymorphisms were genotyped by PCR or PCR-RFLP techniques. T2DM was diagnosed at an earlier age compared to MetS (54 vs 55 years old, p=0.0003) and the difference was greater in carriers of the <i>OXTR</i> G allele (54 vs 56 years old, p=0.0002) or both <i>OXTR</i> G and <i>eNOS</i> b alleles (54 vs 56, p=0.00016). The <i>SOD1</i> AA genotype (O.R.=0.11, p=0.0006) and the presence of both <i>ACE</i> I and <i>OXTR1</i> A (O.R.=0.39, p=0.0005) alleles revealed to be protective for T2DM. <i>SOD1</i> AA and AC genotypes were protective factors for triglyceride (p=0.0002 and p=0.0005, respectively) and HDL cholesterol (p=0.0002 and p=0.0004, respectively) levels in T2DM patients. <i>ACE</i> DD was identified more frequently in hypertensive T2DM patients (O.R.=3.77, p=0.0005) and in those who reported drinking alcohol (p=0.0001) comparing to HC and T2DM patients who did not drink alcohol, respectively. We observed that T2DM patients who reported drinking alcohol had an increased frequency of <i>ACE</i> DD and <i>eNOS</i> bb (p<0.0001), or <i>ACE</i> DD and <i>OXTR</i> G (p<0.0001) compared to non-drinkers. No gene polymorphisms were associated with MetS.</p>","PeriodicalId":55403,"journal":{"name":"Balkan Journal of Medical Genetics","volume":null,"pages":null},"PeriodicalIF":0.5000,"publicationDate":"2023-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/16/8b/bjmg-26-1-bjmg-2023-0003.PMC10413885.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Balkan Journal of Medical Genetics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2478/bjmg-2023-0003","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"GENETICS & HEREDITY","Score":null,"Total":0}
引用次数: 0

Abstract

Type 2 diabetes mellitus (T2DM) and metabolic syndrome (MetS) are diseases caused by the interaction of genetic and non-genetic factors. Therefore, the aim of our study was to investigate the association between six common genetic polymorphisms and T2DM and MetS in males. A total of 120 T2DM, 75 MetS, and 120 healthy controls (HC) were included in the study. ACE ID, eNOS 4a/b, ATR1 A1166C, OXTR (A>G), SOD1 +35A/C, CAT-21A/T gene polymorphisms were genotyped by PCR or PCR-RFLP techniques. T2DM was diagnosed at an earlier age compared to MetS (54 vs 55 years old, p=0.0003) and the difference was greater in carriers of the OXTR G allele (54 vs 56 years old, p=0.0002) or both OXTR G and eNOS b alleles (54 vs 56, p=0.00016). The SOD1 AA genotype (O.R.=0.11, p=0.0006) and the presence of both ACE I and OXTR1 A (O.R.=0.39, p=0.0005) alleles revealed to be protective for T2DM. SOD1 AA and AC genotypes were protective factors for triglyceride (p=0.0002 and p=0.0005, respectively) and HDL cholesterol (p=0.0002 and p=0.0004, respectively) levels in T2DM patients. ACE DD was identified more frequently in hypertensive T2DM patients (O.R.=3.77, p=0.0005) and in those who reported drinking alcohol (p=0.0001) comparing to HC and T2DM patients who did not drink alcohol, respectively. We observed that T2DM patients who reported drinking alcohol had an increased frequency of ACE DD and eNOS bb (p<0.0001), or ACE DD and OXTR G (p<0.0001) compared to non-drinkers. No gene polymorphisms were associated with MetS.

2型糖尿病和代谢综合征的易感性。
2型糖尿病(T2DM)和代谢综合征(MetS)是由遗传因素和非遗传因素相互作用引起的疾病。因此,我们研究的目的是研究6种常见遗传多态性与男性T2DM和MetS之间的关系。该研究共纳入了120例T2DM、75例MetS和120例健康对照(HC)。采用PCR或PCR- rflp技术对ACE ID、eNOS 4a/b、ATR1 A1166C、OXTR (A>G)、SOD1 +35A/C、CAT-21A/T基因多态性进行分型。与met相比,T2DM的诊断年龄更早(54岁对55岁,p=0.0003), OXTR G等位基因携带者(54岁对56岁,p=0.0002)或OXTR G和eNOS b等位基因携带者(54岁对56岁,p=0.00016)的差异更大。SOD1 AA基因型(O.R.=0.11, p=0.0006)和ACE I和oxtr1a等位基因的存在(O.R.=0.39, p=0.0005)显示对T2DM具有保护作用。SOD1 AA和AC基因型是T2DM患者甘油三酯(p=0.0002和p=0.0005)和高密度脂蛋白胆固醇(p=0.0002和p=0.0004)水平的保护因素。与不饮酒的HC和T2DM患者相比,高血压T2DM患者(O.R.=3.77, p=0.0005)和报告饮酒的患者(p=0.0001)发现ACE DD的频率更高。我们观察到,报告饮酒的T2DM患者ACE DD和eNOS bb (pACE DD和OXTR G)的频率增加
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
CiteScore
1.00
自引率
0.00%
发文量
0
审稿时长
>12 weeks
期刊介绍: Balkan Journal of Medical Genetics is a journal in the English language for publication of articles involving all branches of medical genetics: human cytogenetics, molecular genetics, clinical genetics, immunogenetics, oncogenetics, pharmacogenetics, population genetics, genetic screening and diagnosis of monogenic and polygenic diseases, prenatal and preimplantation genetic diagnosis, genetic counselling, advances in treatment and prevention.
×
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