Association Between the Oxytocin Receptor Gene and Amygdalar Volume in Healthy Adults

• Published in: Biological psychiatry (1969) 2010-12, Vol.68 (11), p.1066-1072
• Main Authors: Inoue, Hideyuki, Yamasue, Hidenori, Tochigi, Mamoru, Abe, Osamu, Liu, Xiaoxi, Kawamura, Yoshiya, Takei, Kunio, Suga, Motomu, Yamada, Haruyasu, Rogers, Mark A, Aoki, Shigeki, Sasaki, Tsukasa, Kasai, Kiyoto
• Format: Article
• Language: English
• Subjects: Adult; Age Factors; Alleles; Amygdala; Amygdala - anatomy & histology; Analysis of Variance; autism; Biological and medical sciences; Child clinical studies; Developmental disorders; Female; Gene Frequency; Genetic Association Studies; Genotype; Haplotypes; Humans; Infantile autism; Magnetic Resonance Imaging; Male; Medical sciences; Middle Aged; MRI; Organ Size - genetics; OXTR; oxytocin; Polymorphism, Single Nucleotide; Psychiatry; Psychology. Psychoanalysis. Psychiatry; Psychopathology. Psychiatry; Receptors, Oxytocin - genetics; social dysfunction
• ISSN: 0006-3223; 1873-2402
• DOI: 10.1016/j.biopsych.2010.07.019

Background Recent studies have suggested that oxytocin affects social cognition and behavior mediated by the oxytocin receptor (OXTR) in amygdala in humans as well as in experimental animals. Genetic studies have revealed a link between the OXTR gene and the susceptibility to autism spectrum disorders (ASD), especially in the social dysfunctional feature of ASD. Methods We examined the relationship between amygdala volume measured with manual tracing methodology and seven single nucleotide polymorphisms and one haplotype-block in OXTR , which were previously reported to be associated with ASD, in 208 socially intact Japanese adults with no neuropsychiatric history or current diagnosis. Results The rs2 254298A allele of OXTR was significantly associated with larger bilateral amygdala volume. The rs2 254298A allele effect on amygdala volume varied in proportion to the dose of this allele. The larger the number of rs2 254298A alleles an individual had, the larger their amygdala volume. Such an association was not observed with hippocampal volume or with global brain volumes, including whole gray, white matter, and cerebrospinal-fluid space. Furthermore, two three–single nucleotide polymorphism haplotypes, including rs2 254298G allele, showed significant associations with the smaller bilateral amygdala volume. Conclusions The present results suggest that OXTR might be associated with the susceptibility to ASD, especially in its aspects of social interaction and communication mediated by a modulation of amygdala development, one of the most distributed brain regions with high density of OXTR. Furthermore, amygdala volume measured with magnetic resonance imaging could be a useful intermediate phenotype to uncover the complex link between OXTR and social dysfunction in ASD.