Department of Psychiatry and Psychotherapy, Jena University Hospital, Philosophenweg 3, 07743 Jena, Germany.
J Psychiatr Res. 2012 Dec;46(12):1531-9. doi: 10.1016/j.jpsychires.2012.08.026. Epub 2012 Sep 25.
Common genetic variation in the promoter region of the glutamate receptor delta 1 (GRID1) gene has recently been shown to confer increased risk for schizophrenia in several independent large samples. We analysed high-resolution magnetic resonance imaging (MRI) data from 62 patients with schizophrenia and 54 healthy controls using voxel-based morphometry (VBM) to assess the effect of single nucleotide polymorphism rs3814614 (located in the GRID1 promoter region), of which the T allele was identified as a risk factor in a previous association study. There were no effects of genotype or group × genotype interactions on total brain grey matter or white matter, but on regional grey matter. In healthy subjects, we identified a significant effect of rs3814614 genotype in the anterior thalamus (bilaterally), superior prefrontal cortex, and orbitofrontal cortex - in all cases with the homozygous risk genotype TT resulting in higher grey matter density. We did not find this association within the schizophrenia sample, where rs3814614 variation was only associated with grey matter reduction in TT homozygous subjects in medial parietal cortex and increased grey matter in right medial cerebellum. For white matter, we did not find significant genotype effects in healthy controls, and only minor effects within schizophrenia patients in the posterior temporal lobe white matter. Our data indicate that GRID1 rs3814614 genotype is related to grey matter variation in prefrontal and anterior thalamic brain areas in healthy subjects, but not in patients indicating a potential role of this schizophrenia candidate gene in thalamo-cortical functioning.
最近的研究表明,谷氨酸受体 delta 1(GRID1)基因启动子区域的常见遗传变异与几种独立的大样本中精神分裂症的风险增加有关。我们使用基于体素的形态计量学(VBM)分析了 62 名精神分裂症患者和 54 名健康对照者的高分辨率磁共振成像(MRI)数据,以评估单核苷酸多态性 rs3814614(位于 GRID1 启动子区域)的影响,该等位基因在先前的关联研究中被确定为风险因素。基因型或组×基因型相互作用对总脑灰质或白质没有影响,但对灰质区域有影响。在健康受试者中,我们发现 rs3814614 基因型在前丘脑(双侧)、额上回和眶额皮层中存在显著影响-在所有情况下,纯合风险基因型 TT 导致灰质密度增加。我们在精神分裂症样本中没有发现这种关联,在该样本中,rs3814614 变异仅与 TT 纯合子受试者中内侧顶叶皮质的灰质减少和右侧内侧小脑灰质增加有关。对于白质,我们在健康对照组中没有发现显著的基因型影响,在精神分裂症患者中仅在后颞叶白质中发现较小的影响。我们的数据表明,GRID1 rs3814614 基因型与健康受试者前额叶和前丘脑脑区的灰质变化有关,但在患者中没有,这表明该候选基因在丘脑-皮质功能中可能发挥作用。