Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder

被引:177
作者
Dickel, Diane E.
Veenstra-VanderWeele, Jeremy
Cox, Nancy J.
Wu, Xiaolin
Fischer, Daniel J.
Van Etten-Lee, Michelle
Himle, Joseph A.
Leventhal, Bennett L.
Cook, Edwin H.
Hanna, Gregory L.
机构
[1] Vanderbilt Univ, Med Ctr, Ctr Mol Neurosci, Nashville, TN 37232 USA
[2] Univ Chicago, Dept Human Genet, Chicago, IL USA
[3] Univ Illinois, Dept Psychiat, Inst Juvenile Res, Chicago, IL USA
[4] Univ Michigan, Dept Psychiat, Ann Arbor, MI 48109 USA
[5] Univ Washington, Dept Genome Sci, Seattle, WA USA
关键词
D O I
10.1001/archpsyc.63.7.778
中图分类号
R749 [精神病学];
学科分类号
100205 [精神病与精神卫生学];
摘要
Context: The first 2 independent linkage studies for obsessive-compulsive disorder (OCD) identified a region on 9p24 with suggestive evidence for linkage. The glutamate transporter gene solute carrier family 1, member 1 (SLC1A1) is a promising functional candidate in this region because altered glutamatergic concentrations have been found in the striatum and anterior cingulate in neuroimaging studies of pediatric OCD. Objective: To determine whether genotypes at polymorphisms in the SLC1A1 gene region are associated with early-onset OCD. Design: Family-based analysis of association using the transmission disequilibrium test, confirmed using the family-based association test. Setting: Anxiety disorders program in an academic medical center. Participants: Seventy-one probands with DSM-III-R or DSM-IV OCD and their parents. Methods: Nine single nucleotide polymorphisms spaced throughout the SLC1A1 gene region were genotyped. Results: Significant association was detected at rs3780412 (P=.04) and rs301430 (P=.03), 2 common adjacent single nucleotide polymorphisms in the 3' region of SLC1A1. Analysis by sex revealed that association at rs3780412 was limited to male probands ( P=.002). Significant association was also detected for the T/C haplotype at rs301430-rs301979 ( P=.03), the only haplotype block identified among the 9 single nucleotide polymorphisms. Analysis by sex also revealed that the haplotype association was limited to male probands (P=.003). A deletion in the 3' flanking region of SLC1A1 was also detected that imperfectly segregated with OCD in a large, multigenerational family with multiple affected individuals. Conclusions: The 3' region of SLC1A1 may contain a susceptibility allele for early-onset OCD, with differential effects in males and females. The results also provide further support for the involvement of a glutamatergic dysfunction in the pathogenesis of early-onset OCD.
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收藏
页码:778 / 785
页数:8
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