Investigating the Genetic Basis of Theory of Mind (ToM): The Role of Catechol-O-Methyltransferase (COMT) Gene Polymorphisms

被引:21
作者
Xia, Haiwei [1 ]
Wu, Nan [1 ]
Su, Yanjie [1 ]
机构
[1] Peking Univ, Dept Psychol, Beijing 100871, Peoples R China
基金
中国国家自然科学基金;
关键词
ASPERGER-SYNDROME; METHYL-TRANSFERASE; SCHIZOPHRENIA; BRAIN; AUTISM; ASSOCIATION; DISORDERS; DOPAMINE; STORIES; ABILITY;
D O I
10.1371/journal.pone.0049768
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ability to deduce other persons' mental states and emotions which has been termed 'theory of mind (ToM)' is highly heritable. First molecular genetic studies focused on some dopamine-related genes, while the genetic basis underlying different components of ToM (affective ToM and cognitive ToM) remain unknown. The current study tested 7 candidate polymorphisms (rs4680, rs4633, rs2020917, rs2239393, rs737865, rs174699 and rs59938883) on the catechol-O-methyltransferase (COMT) gene. We investigated how these polymorphisms relate to different components of ToM. 101 adults participated in our study; all were genetically unrelated, non-clinical and healthy Chinese subjects. Different ToM tasks were applied to detect their theory of mind ability. The results showed that the COMT gene rs2020917 and rs737865 SNPs were associated with cognitive ToM performance, while the COMT gene rs5993883 SNP was related to affective ToM, in which a significant gender-genotype interaction was found (p = 0.039). Our results highlighted the contribution of DA-related COMT gene on ToM performance. Moreover, we found out that the different SNP at the same gene relates to the discriminative aspect of ToM. Our research provides some preliminary evidence to the genetic basis of theory of mind which still awaits further studies.
引用
收藏
页数:6
相关论文
共 38 条
[21]   The Strange Stories Test: A replication with high-functioning adults with autism or Asperger syndrome [J].
Jolliffe, T ;
Baron-Cohen, S .
JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 1999, 29 (05) :395-406
[22]   Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatric disorders [J].
Lachman, HM ;
Papolos, DF ;
Saito, T ;
Yu, YM ;
Szumlanski, CL ;
Weinshilboum, RM .
PHARMACOGENETICS, 1996, 6 (03) :243-250
[23]   Dopamine receptor D4 gene variation predicts preschoolers' developing theory of mind [J].
Lackner, Christine ;
Sabbagh, Mark A. ;
Hallinan, Elizabeth ;
Liu, Xudong ;
Holden, Jeanette J. A. .
DEVELOPMENTAL SCIENCE, 2012, 15 (02) :272-280
[24]   Dopaminergic functioning and preschoolers' theory of mind [J].
Lackner, Christine L. ;
Bowman, Lindsay C. ;
Sabbagh, Mark A. .
NEUROPSYCHOLOGIA, 2010, 48 (06) :1767-1774
[25]   Role of Novelty Seeking Personality Traits as Mediator of the Association between COMT and Onset Age of Drug Use in Chinese Heroin Dependent Patients [J].
Li, Ting ;
Yu, Shunying ;
Du, Jiang ;
Chen, Hanhui ;
Jiang, Haifeng ;
Xu, Ke ;
Fu, Yingmei ;
Wang, Dongxiang ;
Zhao, Min .
PLOS ONE, 2011, 6 (08)
[26]   The catechol-O-methyl transferase (COMT) gene and its potential association with schizophrenia: Findings from a large German case-control and family-based sample [J].
Nieratschker, Vanessa ;
Frank, Josef ;
Muehleisen, Thomas W. ;
Strohmaier, Jana ;
Wendland, Jens R. ;
Schumacher, Johannes ;
Treutlein, Jens ;
Breuer, Rene ;
Abou Jamra, Rami ;
Mattheisen, Manuel ;
Herms, Stefan ;
Schmael, Christine ;
Maier, Wolfgang ;
Noethen, Markus M. ;
Cichon, Sven ;
Rietschel, Marcella ;
Schulze, Thomas G. .
SCHIZOPHRENIA RESEARCH, 2010, 122 (1-3) :24-30
[27]   A cognitive endophenotype of autism in families with multiple incidence [J].
Nyden, Agneta ;
Hagberg, Bibbi ;
Gousse, Veronique ;
Rastam, Maria .
RESEARCH IN AUTISM SPECTRUM DISORDERS, 2011, 5 (01) :191-200
[28]   THE GENETIC-BASIS OF COMPLEX HUMAN BEHAVIORS [J].
PLOMIN, R ;
OWEN, MJ ;
MCGUFFIN, P .
SCIENCE, 1994, 264 (5166) :1733-1739
[29]   Influence of dopamine on precursor cell proliferation and differentiation in the embryonic mouse telencephalon [J].
Popolo, M ;
McCarthy, DM ;
Bhide, PG .
DEVELOPMENTAL NEUROSCIENCE, 2004, 26 (2-4) :229-244
[30]  
Sarfati Y, 1997, Cogn Neuropsychiatry, V2, P1, DOI 10.1080/135468097396388