Department of Psychiatry, Virginia Institute for Psychiatric and Behavioral Genetics, Virginia Commonwealth University, Richmond, 23298-0126, USA.
Am J Med Genet B Neuropsychiatr Genet. 2009 Dec 5;150B(8):1128-32. doi: 10.1002/ajmg.b.30935.
Cyclic AMP response element binding protein (CREB) has been implicated in behavioral models of anxiety and depression, antidepressant response in humans, and suicide. One group reported a female-specific association of the CREB1 gene in early-onset Major Depressive Disorder (MDD), while another found no evidence of association with this phenotype. In this study, we sought to examine the evidence for association of the CREB1 gene to MDD and related phenotypes. We used multivariate structural equation modeling to identify and select twin pairs that scored at the extremes of a latent genetic risk factor shared by MDD, neuroticism, and several anxiety disorders from the Virginia Twin Registry. Using one member from each of these pairs, the resulting sample of 589 cases (including 473 subjects with lifetime MDD) and 539 controls were entered into a 2-stage association study in which genetic markers were screened in stage 1, the positive results of which were tested for replication in stage 2. Eight SNP markers selected to capture the major allelic variation across the haplotype block containing CREB1 were analyzed for differences between cases and controls. Several markers showed criterion differences between cases and controls in the stage 1 sample with some evidence of sex specific effects. However, none of these markers were significant in stage 2 in either sex individually or combined. Our data suggests that common variations in the CREB1 gene do not appear to increase susceptibility for MDD or related phenotypes.
环磷酸腺苷反应元件结合蛋白(CREB)与焦虑和抑郁的行为模型、人类的抗抑郁反应和自杀有关。有一个研究小组报告称,在早期发病的重度抑郁症(MDD)患者中,CREB1 基因存在女性特异性关联,而另一个研究小组则没有发现该基因与该表型有关的证据。在这项研究中,我们试图研究 CREB1 基因与 MDD 及相关表型的关联证据。我们使用多元结构方程模型,从弗吉尼亚双胞胎登记处中,确定并选择在 MDD、神经质和几种焦虑障碍的潜在遗传风险因素方面得分处于极端的双胞胎对。使用这些对中的每一对的一个成员,从这些对中的每一对中选取一个成员,得到了一个由 589 例病例(包括 473 例有终生 MDD 的受试者)和 539 名对照组成的样本,这些样本被纳入了一项两阶段关联研究,其中在第一阶段筛选了遗传标记,阳性结果在第二阶段进行了复制测试。分析了 8 个 SNP 标记,这些标记选择来捕获包含 CREB1 的单倍型块中的主要等位基因变异,以比较病例和对照组之间的差异。在第一阶段的样本中,有几个标记在病例和对照组之间存在标准差异,并且存在一些性别特异性效应的证据。然而,在单独或联合的男性或女性中,这些标记在第二阶段均没有达到显著水平。我们的数据表明,CREB1 基因的常见变异似乎不会增加 MDD 或相关表型的易感性。