期刊
BRAIN IMAGING AND BEHAVIOR
卷 3, 期 1, 页码 64-76出版社
SPRINGER
DOI: 10.1007/s11682-008-9050-3
关键词
Obsessive-compulsive disorder; Genetic association; Glutamate; Orbitofrontal cortex; Anterior cingulate cortex; Thalamus
类别
资金
- Ontario Mental Health Foundation
- Canadian Institutes for Health Research [MOP-38077]
- National Alliance on Research in Schizophrenia and Depression
- Obsessive-Compulsive Foundation Research
- Psychiatric Research and Training Program
- Miriam Hamburger Endowed Chair of Child Psychiatry at Children's Hospital of Michigan
- Wayne State University
- National Institute of Mental Health [R01MH59299, K24MH02037]
This pilot study was undertaken to determine if there was a significant association between specific glutamate system genes and regional volumes of interest implicated in the pathogenesis of obsessive-compulsive disorder (OCD). Volumetric magnetic resonance imaging (MRI) and genotyping of seven polymorphisms in two genes, glutamate receptor, ionotropic, N-methyl-d-aspartate 2B (GRIN2B) and solute linked carrier, family 1, member 1 (SLC1A1) were conducted in 31 psychotropic-naive pediatric OCD patients. The rs1805476 variant of GRIN2B was associated with left but not right orbital frontal cortex (OFC) (p=0.04) and right but not left anterior cingulate cortex (ACC) volume (p=0.02). The SLC1A1 rs3056 variant was associated with increased total (p=0.01), left (p=0.02) and right (p=0.02) thalamic volume. These results suggest that GRIN2B and SLC1A1 may be associated with regional volumetric alterations in OFC, ACC, and thalamus in children with OCD.
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