Virginia Institute for Psychiatric and Behavioral Genetics, Department of Psychiatry, Virginia Commonwealth University, Richmond 23298, USA.
JAMA Psychiatry. 2013 Jun;70(6):599-607. doi: 10.1001/jamapsychiatry.2013.751.
We do not know whether the clinical criteria for major depression (MD) reflect a single or multiple dimensions of genetic risk.
To determine the structure of genetic and environmental risk factors for the 9 DSM-IV symptomatic MD criteria.
Population-based twin registry.
Virginia.
Seven thousand five hundred members of adult twin pairs from the Virginia Adult Twin Study of Psychiatric and Substance Use Disorders.
Symptoms of lifetime MD as assessed at personal interview.
The best-fit twin model was multidimensional, requiring 3 genetic, 1 common environmental and 3 unique environmental common factors, and criterion-specific unique environmental factors. The first genetic factor was characterized by high loadings on cognitive and psychomotor depressive symptoms. The second and third genetic factors had strong loadings for mood and neurovegetative depressive symptoms, respectively. Genetic factor scores derived from these 3 factors differentially predicted patterns of comorbidity, other historical/clinical features of MD, and demographic variables. These results suggested that the first genetic factor reflected a general liability to internalizing disorders, while the third genetic factor was more specific for melancholic MD. The 3 unique environmental common factors reflected, respectively, global depressive, core mood, and cognitive depressive symptoms.
The DSM-IV syndrome of MD does not reflect a single dimension of genetic liability. Rather, these criteria reflect 3 underlying dimensions that index genetic risk for cognitive/psychomotor, mood, and neurovegetative symptoms. While in need of replication, these results, validated by predictions using estimated genetic factor scores, have implications for gene-finding efforts for MD.
我们不知道重度抑郁症(MD)的临床标准是否反映了单一或多种遗传风险维度。
确定DSM-IV 症状性 MD 9 项标准的遗传和环境风险因素结构。
基于人群的双胞胎登记处。
弗吉尼亚州。
来自弗吉尼亚成人双胞胎精神和物质使用障碍研究的 7500 名成年双胞胎成员。
通过个人访谈评估的终生 MD 症状。
最佳拟合的双胞胎模型是多维的,需要 3 个遗传、1 个共同环境和 3 个独特环境共同因素,以及特定于标准的独特环境因素。第一个遗传因素的特征是对认知和精神运动性抑郁症状有较高的负荷。第二和第三个遗传因素分别对情绪和神经植物性抑郁症状有较强的负荷。从这 3 个因素中得出的遗传因素得分差异预测了共病模式、MD 的其他历史/临床特征和人口统计学变量。这些结果表明,第一个遗传因素反映了对内化障碍的一般易感性,而第三个遗传因素更具体地反映了忧郁性 MD。3 个独特的环境共同因素分别反映了全球性抑郁、核心情绪和认知性抑郁症状。
DSM-IV MD 综合征并不反映遗传易感性的单一维度。相反,这些标准反映了 3 个潜在的维度,这些维度反映了认知/精神运动、情绪和神经植物性症状的遗传风险。虽然需要复制,但这些结果通过使用估计的遗传因素得分进行预测得到验证,对 MD 的基因发现工作具有启示意义。