ZNF804A Genotype Modulates Neural Activity during Working Memory for Faces

被引:18
作者
Linden, David E. J. [1 ,2 ]
Lancaster, Thomas M. [1 ,3 ]
Wolf, Claudia [4 ]
Baird, Alison [5 ]
Jackson, Margaret C. [4 ]
Johnston, Stephen J. [6 ]
Donev, Rossen [5 ]
Thome, Johannes [7 ]
机构
[1] Cardiff Univ, MRC Ctr Neuropsychiat Genet & Genom, Cardiff CF14 4XN, S Glam, Wales
[2] Cardiff Univ, Neurosci & Mental Hlth Res Inst, Cardiff CF14 4XN, S Glam, Wales
[3] Bangor Univ, Sch Med Sci, Bangor, Gwynedd, Wales
[4] Bangor Univ, Wolfson Ctr Cognit & Clin Neurosci, Sch Psychol, Bangor, Gwynedd, Wales
[5] Swansea Univ, Lab Mol Psychiat & Pharmacol, Inst Life Sci, Sch Med, Swansea, W Glam, Wales
[6] Swansea Univ, Dept Psychol, Swansea, W Glam, Wales
[7] Univ Rostock, Dept Psychiat & Psychotherapy, D-18055 Rostock, Germany
基金
英国惠康基金; 英国生物技术与生命科学研究理事会;
关键词
Emotion; Dorsolateral prefrontal cortex; Genetic imaging; Schizophrenia; Working memory; ZNF804A; SHORT-TERM-MEMORY; EXECUTIVE CONTROL; SOCIAL ANHEDONIA; SCHIZOPHRENIA; INFORMATION; HERITABILITY; INEFFICIENCY; ASSOCIATION; MECHANISMS; COGNITION;
D O I
10.1159/000344001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: Genetic susceptibility to schizophrenia (SZ) has been suggested to influence the cortical systems supporting working memory (WM) and face processing. Genetic imaging studies link the SZ risk variant rs1344706 on the ZNF804A gene to psychosis via alterations in functional brain connectivity during WM, but no work has looked at the effects of ZNF804A on WM with face-processing components. Methods: We therefore investigated healthy controls that were genotyped for rs1344706 with a face WM task during functional magnetic resonance imaging. We suggested that variation at the rs1344706 locus would be associated with similar alterations as patients previously tested using the same WM task for faces. Results: The rs1344706 risk allele was indeed associated with altered activation in the right dorsolateral prefrontal (rDLPFC) cortex. We established that the rDLPFC was activated in a task-dependent manner, suggesting that the differences in activation between rs1344706 genotype groups reflected alterations in task processing. Furthermore, we demonstrated that the rDLPFC region showed significant volumetric overlap with the rDLPFC which had previously been reported to be altered during task processing for patients with SZ. Conclusions: The findings support an association between rs1344706 and alterations in DLPFC activity during WM for faces. We further suggest that WM for faces may be a useful intermediate phenotype in the investigation of genetic susceptibility to psychosis. Copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:84 / 92
页数:9
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