Department of Genetic Epidemiology in Psychiatry, Central Institute of Mental Health, University of Heidelberg, Mannheim, Germany.
Mol Psychiatry. 2012 Sep;17(9):906-17. doi: 10.1038/mp.2011.80. Epub 2011 Jul 12.
Recent molecular studies have implicated common alleles of small to moderate effect and rare alleles with larger effect sizes in the genetic architecture of schizophrenia (SCZ). It is expected that the reliable detection of risk variants with very small effect sizes can only be achieved through the recruitment of very large samples of patients and controls (that is tens of thousands), or large, potentially more homogeneous samples that have been recruited from confined geographical areas using identical diagnostic criteria. Applying the latter strategy, we performed a genome-wide association study (GWAS) of 1169 clinically well characterized and ethnically homogeneous SCZ patients from a confined area of Western Europe (464 from Germany, 705 from The Netherlands) and 3714 ethnically matched controls (1272 and 2442, respectively). In a subsequent follow-up study of our top GWAS results, we included an additional 2569 SCZ patients and 4088 controls (from Germany, The Netherlands and Denmark). Genetic variation in a region on chromosome 11 that contains the candidate genes AMBRA1, DGKZ, CHRM4 and MDK was significantly associated with SCZ in the combined sample (n=11 540; P=3.89 × 10(-9), odds ratio (OR)=1.25). This finding was replicated in 23 206 independent samples of European ancestry (P=0.0029, OR=1.11). In a subsequent imaging genetics study, healthy carriers of the risk allele exhibited altered activation in the cingulate cortex during a cognitive control task. The area of interest is a critical interface between emotion regulation and cognition that is structurally and functionally abnormal in SCZ and bipolar disorder.
最近的分子研究表明,精神分裂症(SCZ)的遗传结构中存在小到中等效应的常见等位基因和大效应的罕见等位基因。预计,只有通过招募大量的患者和对照(即数万人),或者通过在使用相同诊断标准的限定地理区域内招募潜在更同质的大样本,才能可靠地检测到具有非常小效应的风险变异。应用后一种策略,我们对来自西欧一个限定区域(德国 464 例,荷兰 705 例)的 1169 例临床特征良好且种族同质性好的 SCZ 患者和 3714 名种族匹配的对照者(分别为 1272 名和 2442 名)进行了全基因组关联研究(GWAS)。在对我们的 GWAS 结果进行后续的随访研究中,我们纳入了另外 2569 例 SCZ 患者和 4088 名对照者(来自德国、荷兰和丹麦)。包含候选基因 AMBRA1、DGKZ、CHRM4 和 MDK 的染色体 11 上的一个区域的遗传变异与联合样本中的 SCZ 显著相关(n=11540;P=3.89×10(-9),优势比(OR)=1.25)。这一发现在 23206 名欧洲血统的独立样本中得到了复制(P=0.0029,OR=1.11)。在随后的影像遗传学研究中,风险等位基因的健康携带者在认知控制任务中表现出扣带皮层激活改变。该关注区域是情绪调节和认知之间的一个关键接口,在 SCZ 和双相情感障碍中结构和功能异常。