van Grootheest Daniël S, Boomsma Dorret I, Hettema John M, Kendler Kenneth S
Department of Biological Psychology, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Am J Med Genet B Neuropsychiatr Genet. 2008 Jun 5;147B(4):473-8. doi: 10.1002/ajmg.b.30622.
Recent research has shown that obsessive-compulsive symptoms (OCS) differ remarkably among patients and can be divided into several symptom dimensions. OCS are influenced by genetic components, but it is unknown to what extent these symptom dimensions are heritable. The phenotypic heterogeneity also raises the question to what extent the symptom dimensions are influenced by specific or shared genetic factors. We studied a population sample of 1,383 female twins from the Virginia Twin Registry. OCS was measured by a questionnaire with 20 items from the Padua Inventory. After factor analysis, three reliable OC symptom dimensions were retained: Rumination, Contamination, and Checking. These OC dimensions were analyzed with multivariate genetic models to investigate both the overlap and uniqueness of genetic and environmental contributions underlying OC symptom dimensions. The multivariate common pathway model provided the best description of the data. All symptom dimensions share variation with a latent common factor, that is, OC behavior. Variation in this common factor was explained by both genes (36%) and environmental factors (64%). Only the Contamination dimension was influenced by specific genes and seemed to be a relatively independent dimension. The results suggest that a broad OC behavioral phenotype exists, influenced by both genes and nonshared environment. In addition, we found evidence for specific genetic and environmental factors underlying the Contamination dimension. Use of the Contamination dimension could therefore provide a powerful approach for the detection of genetic susceptibility loci that contribute to OCS.
近期研究表明,强迫症症状(OCS)在患者之间存在显著差异,可分为几个症状维度。OCS受遗传因素影响,但这些症状维度的遗传程度尚不清楚。表型异质性也引发了一个问题,即症状维度在多大程度上受特定或共同遗传因素的影响。我们研究了弗吉尼亚双胞胎登记处的1383名女性双胞胎的群体样本。OCS通过一份包含帕多瓦量表20个条目的问卷进行测量。经过因子分析,保留了三个可靠的OC症状维度:反复思考、污染和检查。这些OC维度通过多变量遗传模型进行分析,以研究OC症状维度背后遗传和环境因素的重叠性和独特性。多变量共同路径模型对数据提供了最佳描述。所有症状维度都与一个潜在的共同因素即OC行为存在变异共享。这个共同因素的变异由基因(36%)和环境因素(64%)共同解释。只有污染维度受特定基因影响,似乎是一个相对独立的维度。结果表明,存在一种广泛的OC行为表型,受基因和非共享环境影响。此外,我们发现了污染维度背后特定遗传和环境因素的证据。因此,使用污染维度可能为检测导致OCS的遗传易感性位点提供一种有力方法。