[The Search for Associations of Polymorphic Variants of the COMT and MAOA Genes with Suicide Attempts in Patients with Schizophrenia: A Pilot Study].

Q3 Medicine Molekulyarnaya Biologiya Pub Date : 2026-05-01 DOI:10.7868/S3034555326030061
V V Tiguntsev, I A Mednova, A N Kornetov, D Z Paderina, E G Kornetova, S A Ivanova
{"title":"[The Search for Associations of Polymorphic Variants of the COMT and MAOA Genes with Suicide Attempts in Patients with Schizophrenia: A Pilot Study].","authors":"V V Tiguntsev, I A Mednova, A N Kornetov, D Z Paderina, E G Kornetova, S A Ivanova","doi":"10.7868/S3034555326030061","DOIUrl":null,"url":null,"abstract":"<p><p>The main causes of early mortality in patients with schizophrenia are comorbid somatic diseases (primarily cardiovascular diseases, diabetes, and obesity) and suicide, which reduces life expectancy on average by ten years compared to the general population. The COMT gene encodes catechol-O-methyltransfer- ase. This enzyme is responsible for O-methylation, one of the main pathways for catecholamine inactivation. The MAOA gene encodes monoaminoxidаse type A, an enzyme that carries out oxidative deamination of dopamine, norepinephrine, and serotonin. We hypothesized that polymorphic variants of the COMT and MAOA genes are associated with suicidal behavior in patients with schizophrenia. Accordingly, the aim of our study was to investigate the associations between the presence or absence of a history of suicidal behavior in patients with schizophrenia and polymorphic variants of the COMT and MAOA genes. A total of 150 patients of Slavic ethnicity with schizophrenia were examined. The presence or absence of a history of suicidal tendencies was determined based on medical records and a clinical interview. The control group consisted of 134 apparently healthy military personnel. Seven polymorphic variants in the COMT gene and two polymorphic variants in the MAOA gene were selected for pilot genotyping. Polymorphic variants of the COMT and MAOA genes were initially determined using PCR. An association was found between the COMT rs4680 and rs4633 polymorphic variants and a history of suicide attempts in patients with schizophrenia. The results of our study demonstrate the possible contribution of the catechol-O-methyltransferase gene to the mechanisms of suicidal behavior in patients with schizophrenia.</p>","PeriodicalId":39818,"journal":{"name":"Molekulyarnaya Biologiya","volume":"60 3","pages":"457-473"},"PeriodicalIF":0.0000,"publicationDate":"2026-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molekulyarnaya Biologiya","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.7868/S3034555326030061","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

The main causes of early mortality in patients with schizophrenia are comorbid somatic diseases (primarily cardiovascular diseases, diabetes, and obesity) and suicide, which reduces life expectancy on average by ten years compared to the general population. The COMT gene encodes catechol-O-methyltransfer- ase. This enzyme is responsible for O-methylation, one of the main pathways for catecholamine inactivation. The MAOA gene encodes monoaminoxidаse type A, an enzyme that carries out oxidative deamination of dopamine, norepinephrine, and serotonin. We hypothesized that polymorphic variants of the COMT and MAOA genes are associated with suicidal behavior in patients with schizophrenia. Accordingly, the aim of our study was to investigate the associations between the presence or absence of a history of suicidal behavior in patients with schizophrenia and polymorphic variants of the COMT and MAOA genes. A total of 150 patients of Slavic ethnicity with schizophrenia were examined. The presence or absence of a history of suicidal tendencies was determined based on medical records and a clinical interview. The control group consisted of 134 apparently healthy military personnel. Seven polymorphic variants in the COMT gene and two polymorphic variants in the MAOA gene were selected for pilot genotyping. Polymorphic variants of the COMT and MAOA genes were initially determined using PCR. An association was found between the COMT rs4680 and rs4633 polymorphic variants and a history of suicide attempts in patients with schizophrenia. The results of our study demonstrate the possible contribution of the catechol-O-methyltransferase gene to the mechanisms of suicidal behavior in patients with schizophrenia.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
[寻找COMT和MAOA基因多态性变异与精神分裂症患者自杀企图的关联:一项初步研究]。
精神分裂症患者早期死亡的主要原因是共病躯体疾病(主要是心血管疾病、糖尿病和肥胖)和自杀,这与一般人群相比,平均减少了10年的预期寿命。COMT基因编码儿茶酚o -甲基转移酶。这种酶负责o -甲基化,这是儿茶酚胺失活的主要途径之一。MAOA基因编码单胺氧化酶A型,这是一种对多巴胺、去甲肾上腺素和血清素进行氧化脱胺的酶。我们假设COMT和MAOA基因的多态性变异与精神分裂症患者的自杀行为有关。因此,我们的研究目的是调查精神分裂症患者存在或没有自杀行为史与COMT和MAOA基因多态性变异之间的关系。对150例斯拉夫族精神分裂症患者进行了检查。根据医疗记录和临床访谈确定是否存在自杀倾向史。对照组由134名表面健康的军人组成。选择COMT基因的7个多态性变异和MAOA基因的2个多态性变异进行中试基因分型。COMT和MAOA基因的多态性变异最初是用PCR确定的。发现COMT rs4680和rs4633多态性变异与精神分裂症患者的自杀企图史之间存在关联。我们的研究结果证明了儿茶酚- o -甲基转移酶基因在精神分裂症患者自杀行为机制中的可能作用。
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 去求助
来源期刊
Molekulyarnaya Biologiya
Molekulyarnaya Biologiya Medicine-Medicine (all)
CiteScore
0.70
自引率
0.00%
发文量
131
期刊最新文献
[Yeast as a Biochemical Model for Diseases Associated with Impaired Intracellular Proteolytic Systems]. [The Search for Associations of Polymorphic Variants of the COMT and MAOA Genes with Suicide Attempts in Patients with Schizophrenia: A Pilot Study]. [Effect of ESR1 Somatic Mutations on SERM/SERD Binding: Insights from Molecular Docking and Molecular Dynamics Simulations]. [Modern Methods of Molecular Modeling of Aptamers]. [Cloning of Mycoplasma gallisepticum Genome in Saccharomyces cerevisiae Cells].
wanfang
×
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学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
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