Elsevier

Neuroscience Letters

Volume 417, Issue 1, 24 April 2007, Pages 6-9
Neuroscience Letters

Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism

https://doi.org/10.1016/j.neulet.2007.02.001Get rights and content

Abstract

The oxytocin receptor gene (OXTR) has been studied in autism because of the role of oxytocin (OT) in social cognition. Linkage has also been demonstrated to the region of OXTR in a large sample. Two single nucleotide polymorphisms (SNPs) and a haplotype constructed from them in OXTR have been associated with autism in the Chinese Han population. We tested whether these associations replicated in a Caucasian sample with strictly defined autistic disorder. We genotyped the two previously associated SNPs (rs2254298, rs53576) in 57 Caucasian autism trios. Probands met clinical, ADI-R, and ADOS criteria for autistic disorder. Significant association was detected at rs2254298 (p = 0.03) but not rs53576. For rs2254298, overtransmission of the G allele to probands with autistic disorder was found which contrasts with the overtransmission of A previously reported in the Chinese Han sample. In both samples, G was more frequent than A. However, in our Caucasian autism trios and the CEU Caucasian HapMap samples the frequency of A was less than that reported in the Chinese Han and Chinese in Bejing HapMap samples. The haplotype test of association did not reveal excess transmission from parents to affected offspring. These findings provide support for association of OXTR with autism in a Caucasian population. Overtransmission of different alleles in different populations may be due to a different pattern of linkage disequilibrium between the marker rs2254298 and an as yet undetermined susceptibility variant in OXTR.

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Acknowledgments

The authors are especially grateful to the families who participated in the study. Kathy Hennessy provided expert technical assistance and Jeremy Veenstra-VanderWeele provided assistance with statistical programs. This work was supported, in part, by NIH U19 HD35482 (E.C., C.L.), R01 MH066496 (C.L.), 5T32MH7631 (S.J.), the Jean Young and Walden W. Shaw Foundation, the Harris Foundation (C.W.B.), and the Children's Brain Research Foundation (E.C.).

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