Levinson Douglas F, Zubenko George S, Crowe Raymond R, DePaulo Raymond J, Scheftner William S, Weissman Myrna M, Holmans Peter, Zubenko Wendy N, Boutelle Sandra, Murphy-Eberenz Kathleen, MacKinnon Dean, McInnis Melvin G, Marta Diana H, Adams Philip, Sassoon Stephanie, Knowles James A, Thomas Jo, Chellis Jennifer
Department of Psychiatry and Center for Neurobiology and Behavior, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104-3309, USA.
Am J Med Genet B Neuropsychiatr Genet. 2003 May 15;119B(1):118-30. doi: 10.1002/ajmg.b.20009.
This is an initial report on a six-site collaborative project, Genetics of Recurrent Early-Onset Depression (GenRED). This is a study of a large sample of families with recurrent major depressive disorder (DSM-IV) beginning by the age 30 in probands or 40 in relatives. Evidence suggests that early onset and recurrence of depressive episodes predict substantially increased risk of depression in first-degree relatives compared with the general population, suggesting that susceptibility genes might be mapped with this phenotype. The projected sample of 800-1,000 affected sibling pairs (ASPs) and other relatives will be studied using genome scan methods. Biological materials and blinded clinical data will be made available through the NIMH cell repository program. The sample should have good-to-excellent power to detect a locus associated with a 24% or greater population-wide increase in risk to siblings. We describe 838 affected individuals from the first 305 families containing 434 independent ASPs, or 613 ASPs counting all possible pairs. The mean age at the onset was 18.5 years, with a mean of 7.3 episodes and longest episode of 655 days. Almost all subjects had experienced at least 4 weeks of depression with five or more additional symptom criteria. Frequencies of symptoms and psychiatric and medical comorbid are provided. Substance use was more common in males, and panic disorder in females. Within pairs of affected siblings, correlations were significant for age at onset, substance abuse/dependence, panic disorder, obsessive-compulsive disorder and nicotine initiation and persistence. We replicated previously reported associations among comorbid panic disorder and social phobia, chronicity of depression and suicidal behavior. This suggests comparability of our cases to those in earlier large family studies. This dataset should prove useful for genetic studies of a highly familial form of major depressive disorder.
这是一份关于一项六中心合作项目——复发性早发性抑郁症遗传学研究(GenRED)的初步报告。该研究针对大量先证者30岁前或亲属40岁前起病的复发性重度抑郁症(DSM-IV)家庭样本展开。有证据表明,与普通人群相比,抑郁发作的早发和复发预示着一级亲属患抑郁症的风险大幅增加,这表明可能可以通过这种表型来定位易感基因。预计将使用基因组扫描方法对800 - 1000对患病同胞对(ASP)及其他亲属进行研究。生物材料和盲态临床数据将通过美国国立精神卫生研究所(NIMH)细胞库项目提供。该样本应有良好至极佳的能力来检测与同胞患风险在全人群中增加24%或更多相关的基因座。我们描述了来自前305个家庭的838名患病个体,其中包含434对独立的ASP,若计算所有可能的对子则为613对ASP。发病的平均年龄为18.5岁,平均发作7.3次,最长发作持续655天。几乎所有受试者都经历了至少4周的抑郁,且有五项或更多其他症状标准。提供了症状以及精神和医学共病的频率。物质使用在男性中更常见,惊恐障碍在女性中更常见。在患病同胞对中,发病年龄、物质滥用/依赖、惊恐障碍、强迫症以及尼古丁开始使用和持续使用之间的相关性显著。我们重复了先前报道的共病惊恐障碍与社交恐惧症、抑郁症慢性化与自杀行为之间的关联。这表明我们的病例与早期大型家系研究中的病例具有可比性。该数据集应会被证明对高度家族性形式的重度抑郁症的遗传学研究有用。