• 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

面孔认知的遗传基础及其与流体认知能力的关系。

On the genetic basis of face cognition and its relation to fluid cognitive abilities.

机构信息

Department of Individual Differences and Psychological Assessment, University of Ulm, 89069 Ulm, Germany.

出版信息

Genes Brain Behav. 2013 Jun;12(4):438-45. doi: 10.1111/gbb.12034. Epub 2013 Apr 15.

DOI:10.1111/gbb.12034
PMID:23489762
Abstract

The oxytocin and the dopaminergic systems have turned out to be highly relevant for social abilities and cognition. Therefore, we examined the association between two functional gene polymorphisms and face cognition (FC) in a multivariate study (N = 250) by applying structural equation modeling. The catechol-O-methyltransferase (COMT) val158met polymorphism influences the enzyme activity of COMT, which affects the prefrontal dopamine concentration. The rs226849 is a single-nucleotide polymorphism located in the promoter region of the oxytocin receptor (OXTR) gene, modulating the mRNA expression. By modeling a general fluid ability factor (defined by working memory and reasoning) and nested FC factors, we tested genetic contributions to FC, after controlling for variance in FC that was also associated with fluid abilities. In line with several previous studies, we found a significant association between the COMT genotype and fluid abilities (Gf) but not with FC. The association between the oxytocin polymorphism and Gf was opposite in direction for men and women. Women with the C(+) genotype performed better on Gf tasks than those with the C(-) genotype. Conversely, men with the C(-) genotype performed better than those with the C(+) genotype. There was no significant association between OXTR and the nested FC factor. Therefore, the relationship between the oxytocin polymorphism and FC can be fully accounted for by Gf. The sex specificity of this relationship is a novel finding and warrants a mechanistic explanation.

摘要

催产素和多巴胺系统已被证明与社交能力和认知高度相关。因此,我们通过结构方程模型,在一项多元研究(N=250)中,检查了两种功能基因多态性与面孔认知(FC)之间的关联。儿茶酚-O-甲基转移酶(COMT)val158met 多态性影响 COMT 的酶活性,从而影响前额叶多巴胺浓度。rs226849 是位于催产素受体(OXTR)基因启动子区域的单核苷酸多态性,调节 mRNA 表达。通过构建一般流体能力因素(由工作记忆和推理定义)和嵌套的 FC 因素模型,我们在控制与流体能力相关的 FC 方差后,测试了遗传对 FC 的贡献。与几项先前的研究一致,我们发现 COMT 基因型与流体能力(Gf)之间存在显著关联,但与 FC 无关。催产素多态性与 Gf 之间的关联在男性和女性之间的方向相反。C(+) 基因型的女性在 Gf 任务上的表现优于 C(-) 基因型的女性。相反,C(-) 基因型的男性比 C(+) 基因型的男性表现更好。OXTR 与嵌套的 FC 因子之间没有显著关联。因此,催产素多态性与 FC 之间的关系可以完全由 Gf 来解释。这种关系的性别特异性是一个新发现,需要进行机制解释。

相似文献

1
On the genetic basis of face cognition and its relation to fluid cognitive abilities.面孔认知的遗传基础及其与流体认知能力的关系。
Genes Brain Behav. 2013 Jun;12(4):438-45. doi: 10.1111/gbb.12034. Epub 2013 Apr 15.
2
Catechol O-methyltransferase Val158Met polymorphism is associated with cognitive performance in nondemented adults.儿茶酚-O-甲基转移酶Val158Met多态性与非痴呆成年人的认知表现相关。
J Cogn Neurosci. 2005 Jul;17(7):1018-25. doi: 10.1162/0898929054475136.
3
How to consistently link extraversion and intelligence to the catechol-O-methyltransferase (COMT) gene: on defining and measuring psychological phenotypes in neurogenetic research.如何将外向型和智力与儿茶酚-O-甲基转移酶(COMT)基因联系起来:在神经遗传学研究中定义和测量心理表型。
J Pers Soc Psychol. 2012 Feb;102(2):427-44. doi: 10.1037/a0026544. Epub 2011 Dec 19.
4
Association between hypnotizability and the catechol-O-methyltransferase (COMT) polymorphism.催眠易感性与儿茶酚-O-甲基转移酶(COMT)多态性之间的关联。
Int J Clin Exp Hypn. 2010 Jul;58(3):301-15. doi: 10.1080/00207141003760827.
5
Association of catechol-O-methyltransferase (COMT) polymorphism and academic achievement in a Chinese cohort.中国队列中儿茶酚-O-甲基转移酶(COMT)基因多态性与学业成绩的关联
Brain Cogn. 2009 Dec;71(3):300-5. doi: 10.1016/j.bandc.2009.07.011. Epub 2009 Aug 22.
6
Catechol-O-methyltransferase val158met and cognitive function in Parkinson's disease.儿茶酚-O-甲基转移酶 val158met 与帕金森病的认知功能。
Mov Disord. 2010 Nov 15;25(15):2550-4. doi: 10.1002/mds.23319.
7
COMT genotype increases risk for bipolar I disorder and influences neurocognitive performance.儿茶酚-O-甲基转移酶基因分型增加了I型双相情感障碍的风险,并影响神经认知表现。
Bipolar Disord. 2007 Jun;9(4):370-6. doi: 10.1111/j.1399-5618.2007.00384.x.
8
Influence of the COMT genotype on working memory and brain activity changes during development.COMT 基因型对工作记忆和大脑活动发育变化的影响。
Biol Psychiatry. 2011 Aug 1;70(3):222-9. doi: 10.1016/j.biopsych.2011.02.027. Epub 2011 Apr 22.
9
The association between the Val158Met polymorphism of the catechol-O-methyl transferase gene and morphological abnormalities of the brain in chronic schizophrenia.儿茶酚-O-甲基转移酶基因Val158Met多态性与慢性精神分裂症患者脑形态异常的关联
Brain. 2006 Feb;129(Pt 2):399-410. doi: 10.1093/brain/awh702. Epub 2005 Dec 5.
10
Differential effect of catechol-O-methyltransferase Val158Met genotype on emotional recognition abilities in healthy men and women.儿茶酚-O-甲基转移酶Val158Met基因多态性对健康男性和女性情绪识别能力的差异影响。
J Int Neuropsychol Soc. 2007 Sep;13(5):881-7. doi: 10.1017/S1355617707070932. Epub 2007 May 18.

引用本文的文献

1
Systematic review reveals multiple sexually antagonistic polymorphisms affecting human disease and complex traits.系统综述揭示了多种与性拮抗相关的多态性,这些多态性影响着人类疾病和复杂特征。
Evolution. 2021 Dec;75(12):3087-3097. doi: 10.1111/evo.14394. Epub 2021 Nov 12.
2
Reflections and New Perspectives on Face Cognition as a Specific Socio-Cognitive Ability.作为一种特定社会认知能力的面部认知的反思与新视角
J Intell. 2021 Jun 11;9(2):30. doi: 10.3390/jintelligence9020030.
3
Individual Differences in the Speed of Facial Emotion Recognition Show Little Specificity but Are Strongly Related with General Mental Speed: Psychometric, Neural and Genetic Evidence.
面部表情识别速度的个体差异特异性不强,但与一般心理速度密切相关:心理测量、神经和遗传证据。
Front Behav Neurosci. 2017 Aug 10;11:149. doi: 10.3389/fnbeh.2017.00149. eCollection 2017.
4
Examining age-related shared variance between face cognition, vision, and self-reported physical health: a test of the common cause hypothesis for social cognition.探究面部认知、视力与自我报告的身体健康之间与年龄相关的共同方差:对社会认知的共同原因假说的一项检验。
Front Psychol. 2015 Aug 12;6:1189. doi: 10.3389/fpsyg.2015.01189. eCollection 2015.
5
Genetic Addiction Risk Score (GARS): molecular neurogenetic evidence for predisposition to Reward Deficiency Syndrome (RDS).遗传成瘾风险评分(GARS):奖赏缺乏综合征(RDS)易感性的分子神经遗传学证据。
Mol Neurobiol. 2014 Dec;50(3):765-96. doi: 10.1007/s12035-014-8726-5. Epub 2014 May 31.
6
An interaction between oxytocin and a genetic variation of the oxytocin receptor modulates amygdala activity toward direct gaze: evidence from a pharmacological imaging genetics study.催产素与催产素受体基因变异的相互作用调节了杏仁核对直接注视的活动:来自药理学成像遗传学研究的证据。
Eur Arch Psychiatry Clin Neurosci. 2013 Nov;263 Suppl 2:S169-75. doi: 10.1007/s00406-013-0452-x. Epub 2013 Sep 27.