• 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

基因变异与发展心理理论之间并无关联:候选基因研究的预先注册复制尝试。

No links between genetic variation and developing theory of mind: A preregistered replication attempt of candidate gene studies.

机构信息

Max Planck Institute for Innovation and Competition, Munich, Germany.

Department of Economics, Ludwig-Maximilians-Universität, Munich, Germany.

出版信息

Dev Sci. 2021 Sep;24(5):e13100. doi: 10.1111/desc.13100. Epub 2021 Mar 5.

DOI:10.1111/desc.13100
PMID:33666309
Abstract

Genetic variability is being discussed as a source of inter-individual differences in Theory of Mind development. Previous studies documented an association between variations in DRD4 VNTR 48 bp, OXTR rs53576, COMT rs4680, and Theory of Mind task performance. As empirical evidence on these associations is sparse, we conducted a preregistered replication attempt of a study reporting a link between DRD4 VNTR 48 bp and false belief understanding in 50-month-old children [Lackner, C., Sabbagh, M. A., Hallinan, E., Liu, X., & Holden, J. J. (2012). Developmental Science, 15(2), 272-280.]. Additionally, we attempted a replication of studies on the role of OXTR rs53576 and COMT rs4680 in Theory of Mind. In both replication attempts, we did not find any evidence for associations between the sampled genetic markers and Theory of Mind ability in a series of analyses. Extending the replication attempt of Lackner et al., we employed longitudinal data from several tasks and measurement points, which allowed us to run follow-up robustness checks with more reliable scores. These extensive analyses corroborated our null finding. This comprehensive non-replication is important to balance current research on genetic markers of Theory of Mind. In a combined evaluation of our own and previous studies, we point to substantial methodological issues that research on the genetic basis of Theory of Mind development faces. We conclude that these limitations currently prevent firm conclusions on genetic influences on Theory of Mind development.

摘要

遗传变异性被认为是心理理论发展中个体间差异的一个来源。先前的研究记录了 DRD4 VNTR 48bp、OXTR rs53576、COMT rs4680 与心理理论任务表现之间的变异关联。由于这些关联的经验证据很少,我们对一项研究进行了预先注册的复制尝试,该研究报告了 DRD4 VNTR 48bp 与 50 个月大儿童错误信念理解之间的联系[Lackner,C.,Sabbagh,M. A.,Hallinan,E.,Liu,X.,&Holden,J. J.(2012)。发展科学,15(2),272-280]。此外,我们还尝试了对 OXTR rs53576 和 COMT rs4680 在心理理论中作用的研究进行复制。在这两项复制尝试中,我们在一系列分析中均未发现采样遗传标记与心理理论能力之间存在关联的证据。在 Lackner 等人的复制尝试中,我们使用了来自多个任务和测量点的纵向数据,这使我们能够使用更可靠的分数进行后续稳健性检查。这些广泛的分析证实了我们的零假设。这种全面的非复制对于平衡当前关于心理理论遗传标记的研究非常重要。在对我们自己和以前的研究进行综合评估时,我们指出了心理理论发展的遗传基础研究面临的实质性方法问题。我们的结论是,这些限制目前阻止了对心理理论发展的遗传影响做出明确的结论。

相似文献

1
No links between genetic variation and developing theory of mind: A preregistered replication attempt of candidate gene studies.基因变异与发展心理理论之间并无关联:候选基因研究的预先注册复制尝试。
Dev Sci. 2021 Sep;24(5):e13100. doi: 10.1111/desc.13100. Epub 2021 Mar 5.
2
Dopamine receptor D4 gene variation predicts preschoolers' developing theory of mind.多巴胺受体 D4 基因变异可预测学龄前儿童心理理论的发展。
Dev Sci. 2012 Mar;15(2):272-80. doi: 10.1111/j.1467-7687.2011.01124.x. Epub 2011 Dec 3.
3
Investigating the genetic basis of theory of mind (ToM): the role of catechol-O-methyltransferase (COMT) gene polymorphisms.探讨心理理论(ToM)的遗传基础:儿茶酚-O-甲基转移酶(COMT)基因多态性的作用。
PLoS One. 2012;7(11):e49768. doi: 10.1371/journal.pone.0049768. Epub 2012 Nov 27.
4
COMT x DRD4 epistasis impacts prefrontal cortex function underlying response control.COMT x DRD4 上位性影响反应控制的前额叶皮层功能。
Cereb Cortex. 2013 Jun;23(6):1453-62. doi: 10.1093/cercor/bhs132. Epub 2012 May 22.
5
Serotonin and Dopamine Gene Variation and Theory of Mind Decoding Accuracy in Major Depression: A Preliminary Investigation.血清素和多巴胺基因变异与重度抑郁症中的心理理论解码准确性:一项初步调查
PLoS One. 2016 Mar 14;11(3):e0150872. doi: 10.1371/journal.pone.0150872. eCollection 2016.
6
The interaction between oxytocin receptor gene methylation and maternal behavior on children's early theory of mind abilities.催产素受体基因甲基化与母婴行为对儿童早期心理理论能力的影响。
Dev Psychopathol. 2020 May;32(2):511-519. doi: 10.1017/S0954579419000257.
7
Association analysis of the DRD4 and COMT genes in methamphetamine abuse.甲基苯丙胺滥用中DRD4基因与COMT基因的关联分析
Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):120-4. doi: 10.1002/ajmg.b.30024.
8
Candidate genes for novelty-seeking: a meta-analysis of association studies of DRD4 exon III and COMT Val158Met.寻求新奇行为的候选基因:对多巴胺D4受体基因(DRD4)第三外显子和儿茶酚-O-甲基转移酶基因(COMT)缬氨酸158位甲硫氨酸多态性关联研究的荟萃分析
Psychiatr Genet. 2018 Dec;28(6):97-109. doi: 10.1097/YPG.0000000000000209.
9
Preliminary Evidence for an Association Between Variants of the Catechol-O-Methyltransferase (COMT) Gene and Premature Ejaculation.儿茶酚氧位甲基转移酶(COMT)基因变异与早泄相关性的初步证据。
J Sex Med. 2017 Dec;14(12):1558-1565. doi: 10.1016/j.jsxm.2017.11.002.
10
Monitoring antisaccades: inter-individual differences in cognitive control and the influence of COMT and DRD4 genotype variations.监测反扫视:认知控制的个体间差异以及 COMT 和 DRD4 基因型变异的影响。
Exp Brain Res. 2010 Jun;203(2):453-63. doi: 10.1007/s00221-010-2250-2. Epub 2010 Apr 24.

引用本文的文献

1
Theory of Mind: A Brief Review of Candidate Genes.心智理论:候选基因的简要综述。
Genes (Basel). 2024 May 31;15(6):717. doi: 10.3390/genes15060717.
2
Association of verbal and non-verbal theory of mind abilities with non-coding variants of OXTR in youth with autism spectrum disorder and typically developing individuals: a case-control study.自闭症谱系障碍和典型发育个体中言语和非言语心理理论能力与 OXTR 非编码变异的关联:病例对照研究。
BMC Psychiatry. 2024 Jan 8;24(1):30. doi: 10.1186/s12888-023-05461-w.
3
Detection, processing and reinforcement of social cues: regulation by the oxytocin system.
检测、处理和强化社会线索:由催产素系统调节。
Nat Rev Neurosci. 2023 Dec;24(12):761-777. doi: 10.1038/s41583-023-00759-w. Epub 2023 Oct 27.
4
Oxytocin-a social peptide? Deconstructing the evidence.催产素——一种社交肽?对证据的解构。
Philos Trans R Soc Lond B Biol Sci. 2022 Aug 29;377(1858):20210055. doi: 10.1098/rstb.2021.0055. Epub 2022 Jul 11.