ARVCF Genetic Influences on Neurocognitive and Neuroanatomical Intermediate Phenotypes in Chinese Patients With Schizophrenia

被引:14
|
作者
Sim, Kang [1 ,2 ]
Chan, Wai-Yen
Woon, Puay-San [1 ]
Low, Hui-Qi [3 ]
Lim, Linda [3 ]
Yang, Guo-Liang [4 ]
Lee, Jimmy [1 ,2 ]
Chong, Siow Ann [2 ]
Sitoh, Yih-Yian [5 ]
Chan, Yiong Huak [1 ,6 ]
Liu, Jianjun [3 ]
Tan, Ene Choo [7 ]
Williams, Hywel [8 ,9 ]
Nowinski, Wieslaw Lucjan [4 ]
机构
[1] Woodbridge Hosp, Dept Gen Psychiat, Inst Mental Hlth, Singapore 539747, Singapore
[2] Inst Mental Hlth, Div Res, Singapore, Singapore
[3] Genome Inst Singapore, Agcy Sci Technol & Res, Singapore, Singapore
[4] Singapore Bioimaging Consortium, Agcy Sci Technol & Res, Biomed Imaging Lab, Singapore, Singapore
[5] Natl Neurosci Inst, Dept Neuroradiol, Singapore, Singapore
[6] Natl Univ Singapore, Dept Biostat, Singapore 117548, Singapore
[7] Kerdang Kerbau Hosp, KK Res Ctr, Singapore, Singapore
[8] Cardiff Univ, Sch Med, MRC Ctr Neuropsychiat Genet & Genom, Cardiff, S Glam, Wales
[9] Cardiff Univ, Sch Med, Dept Psychol Med & Neurol, Cardiff, S Glam, Wales
关键词
QUANTITATIVE TRAIT LOCI; CARDIO-FACIAL SYNDROME; HAPLOTYPIC ASSOCIATION; CHROMOSOME; 22Q11; BRAIN ATLASES; BASAL GANGLIA; LINKAGE PHASE; FAMILY; EXPRESSION; DELETION;
D O I
10.4088/JCP.10m06491
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objective: There are notable similarities between velocardiofacial syndrome and schizophrenia in terms of neurocognitive deficits and brain structural abnormalities. These similarities have supported the role of the armadillo repeat gene deleted in velocardiofacial syndrome (ARVCF) as a susceptibility gene in schizophrenia. This study investigated the relationships between haplotypes of the ARVCF gene and specific intermediate phenotypes in schizophrenia. We hypothesized that ARVCF gene haplotypes influence caudate nucleus volume, fractional anisotropy, and neurocognitive functioning in schizophrenia. Method: Between May 2006 and November 2009, 200 Chinese participants (125 patients with DSM-IV diagnosis of schizophrenia and 75 controls) were genotyped using blood samples, and a subset of 166 participants (99 patients with DSM-/Vdiagnosis of schizophrenia and 67 controls) underwent structural magnetic resonance imaging, diffusion tensor imaging, and completed neuropsychological testing. Results:The haplotype T-G-A-T-T-G-G-C-T-G-T (ARVCF-Hap1) was significantly associated with fractional anisotropy of the caudate nucleus and executive functioning in patients. Specifically, patients with more copies of ARVCF-Hap1 have lower white matter integrity in caudate nucleus (P=.0008) and greater perseverative errors (P=.00003) on the Wisconsin Card Sorting Test. A trend of lower caudate volume (P=.015) in patients with more copies of ARVCF-Hap1 was also observed. Conclusions: These findings are consistent with known ARVCF gene effects on neurodevelopment in terms of cellular arrangement, migration, and intracellular signaling involving the striatum and may involve interactions with other brain networks such as prefrontal cortex, and they underscore the importance of imaging-genetic studies to elucidate the genetic influences underlying intermediate phenotypes in complex neurobehavioral disorders. J Clin Psychiatry 2012;73(3):320-326 (C) Copyright 2011 Physicians Postgraduate Press, Inc.
引用
收藏
页码:320 / 326
页数:7
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