Oxytocin Receptor Genotype Modulates Ventral Striatal Activity to Social Cues and Response to Stressful Life Events

被引:48
|
作者
Loth, Eva [1 ,2 ]
Poline, Jean-Baptiste [4 ]
Thyreau, Benjamin [4 ]
Jia, Tianye [1 ,2 ]
Tao, Chenyang [7 ]
Lourdusamy, Anbarasu [1 ,2 ]
Stacey, David [1 ,2 ]
Cattrell, Anna [1 ,2 ]
Desrivieres, Sylvane [1 ,2 ]
Ruggeri, Barbara [1 ,2 ]
Fritsch, Virgile [4 ]
Banaschewski, Tobias [8 ]
Barker, Gareth J. [1 ]
Bokde, Arun L. W. [14 ]
Buechel, Christian [10 ]
Carvalho, Fabiana M. [1 ,2 ]
Conrod, Patricia J. [1 ,15 ]
Fauth-Buehler, Mira [8 ]
Flor, Herta [8 ]
Gallinat, Jurgen [11 ]
Garavan, Hugh [14 ,19 ]
Heinz, Andreas [11 ]
Bruehl, Ruediger
Lawrence, Claire [3 ]
Mann, Karl [9 ]
Martinot, Jean-Luc [5 ,6 ]
Nees, Frauke [8 ]
Paus, Tomas [3 ,16 ,17 ]
Pausova, Zdenka [18 ]
Poustka, Luise [8 ]
Rietschel, Marcella [8 ]
Smolka, Michael [8 ,12 ,13 ]
Struve, Maren
Feng, Jianfeng [20 ]
Schumann, Gunter [1 ]
机构
[1] Kings Coll London, Inst Psychiat, London WC2R 2LS, England
[2] MRC Social, Genet & Dev Psychiat Ctr, London, England
[3] Univ Nottingham, Sch Psychol, Nottingham, England
[4] CEA Saclay Ctr, Gif Sur Yvette, France
[5] Univ Paris Sud, Inst Natl Sant & Rech Med, INSERM, CEA Unit 1000 Imaging & Psychiat, Paris, France
[6] Univ Paris 05, AP HP, Dept Adolescent Psychopathol & Med, Paris, France
[7] Fudan Univ, Ctr Computat Syst Biol, Sch Math Sci, Shanghai 200433, Peoples R China
[8] Univ Mannheim, Cent Inst Mental Hlth, Mannheim, Germany
[9] Heidelberg Univ, Med Fac Mannheim, Cent Inst Mental Hlth, Dept Addict Behaviour & Addict Med, Mannheim, Germany
[10] Univ Med Ctr Hamburg Eppendorf, Hamburg, Germany
[11] Charite, Dept Psychiat & Psychotherapy, Berlin, Germany
[12] Tech Univ Dresden, Dept Psychiat & Psychotherapy, Dresden, Germany
[13] Tech Univ Dresden, Neuroimaging Ctr, Dept Psychol, Dresden, Germany
[14] Trin Coll, Inst Neurosci, Dublin, Ireland
[15] Univ Montreal, CHU St Justine Hosp, Dept Psychiat, Montreal, PQ H3C 3J7, Canada
[16] Rotman Res Inst, Toronto, ON, Canada
[17] McGill Univ, Montreal Neurol Inst, Montreal, PQ, Canada
[18] Univ Toronto, Hosp Sick Children, Toronto, ON, Canada
[19] Univ Vermont, Dept Psychiat & Psychol, Burlington, ON, Canada
[20] Univ Warwick, Dept Comp Sci, Coventry CV4 7AL, W Midlands, England
基金
英国医学研究理事会; 瑞典研究理事会;
关键词
Amygdala; functional magnetic resonance imaging; genetics; oxytocin; social behavior; ventral striatum; SEX-DIFFERENCES; HUMAN AMYGDALA; BEHAVIOR; BRAIN; GENE; FACES; ASSOCIATION; VASOPRESSIN; PSYCHOPATHOLOGY; DEPRESSION;
D O I
10.1016/j.biopsych.2013.07.043
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Common variants in the oxytocin receptor gene (OXTR) have been shown to influence social and affective behavior and to moderate the effect of adverse experiences on risk for social-affective problems. However, the intermediate neurobiological mechanisms are not fully understood. Although human functional neuroimaging studies have reported that oxytocin effects on social behavior and emotional states are mediated by amygdala function, animal models indicate that oxytocin receptors in the ventral striatum (VS) modulate sensitivity to social reinforcers. This study aimed to comprehensively investigate OXTR-dependent brain mechanisms associated with social-affective problems. Methods: In a sample of 1445 adolescents we tested the effect of 23-tagging single nucleotide polymorphisms across the OXTR region and stressful life events (SLEs) on functional magnetic resonance imaging blood oxygen level-dependent activity in the VS and amygdala to animated angry faces. Single nucleotide polymorphisms for which gene-wide significant effects on brain function were found were then carried forward to examine associations with social-affective problems. Results: A gene-wide significant effect of rs237915 showed that adolescents with minor CC-genotype had significantly lower VS activity than CT/TT-carriers. Significant or nominally significant gene x environment effects on emotional problems (in girls) and peer problems (in boys) revealed a strong increase in clinical symptoms as a function of SLEs in CT/TT-carriers but not CC-homozygotes. However, in low-SLE environments, CC-homozygotes had more emotional problems (girls) and peer problems (boys). Moreover, among CC-homozygotes, reduced VS activity was related to more peer problems. Conclusions: These findings suggest that a common OXTR-variant affects brain responsiveness to negative social cues and that in "riskcarriers" reduced sensitivity is simultaneously associated with more social-affective problems in "favorable environments" and greater resilience against stressful experiences.
引用
收藏
页码:367 / 376
页数:10
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