Zilhão Nuno R, Smit Dirk J, Boomsma Dorret I, Cath Danielle C
Department of Clinical and Health Psychology, Utrecht University, Utrecht, Netherlands; Department of Biological Psychology, Vrije Universiteit, Amsterdam, Netherlands.
Department of Biological Psychology, Vrije Universiteit, Amsterdam, Netherlands; Neuroscience Campus Amsterdam, Vrije Universiteit, Amsterdam, Netherlands.
Front Psychiatry. 2016 Jun 30;7:120. doi: 10.3389/fpsyt.2016.00120. eCollection 2016.
Hoarding, obsessive-compulsive disorder (OCD), and Tourette's disorder (TD) are psychiatric disorders that share symptom overlap, which might partly be the result of shared genetic variation. Population-based twin studies have found significant genetic correlations between hoarding and OCD symptoms, with genetic correlations varying between 0.1 and 0.45. For tic disorders, studies examining these correlations are lacking. Other lines of research, including clinical samples and GWAS or CNV data to explore genetic relationships between tic disorders and OCD, have only found very modest if any shared genetic variation. Our aim was to extend current knowledge on the genetic structure underlying hoarding, OC symptoms (OCS), and lifetime tic symptoms and, in a trivariate analysis, assess the degree of common and unique genetic factors contributing to the etiology of these disorders. Data have been gathered from participants in the Netherlands Twin Register comprising a total of 5293 individuals from a sample of adult monozygotic (n = 2460) and dizygotic (n = 2833) twin pairs (mean age 33.61 years). The data on Hoarding, OCS, and tic symptoms were simultaneously analyzed in Mplus. A liability threshold model was fitted to the twin data, analyzing heritability of phenotypes and of their comorbidity. Following the criteria for a probable clinical diagnosis in all phenotypes, 6.8% of participants had a diagnosis of probable hoarding disorder (HD), 6.3% of OCS, and 12.8% of any probable lifetime tic disorder. Genetic factors explained 50.4, 70.1, and 61.1% of the phenotypic covariance between hoarding-OCS, hoarding-tics, and OCS-tics, respectively. Substantial genetic correlations were observed between hoarding and OCS (0.41), hoarding and tics (0.35), and between OCS and tics (0.37). These results support the contribution of genetic factors in the development of these disorders and their comorbidity. Furthermore, tics were mostly influenced by specific environmental factors unshared with OCS and HD.
囤积症、强迫症(OCD)和抽动秽语综合征(TD)是存在症状重叠的精神疾病,这可能部分是由于共享基因变异所致。基于人群的双胞胎研究发现,囤积症与强迫症症状之间存在显著的遗传相关性,遗传相关性在0.1至0.45之间变化。对于抽动障碍,缺乏检验这些相关性的研究。其他研究方向,包括利用临床样本以及全基因组关联研究(GWAS)或拷贝数变异(CNV)数据来探索抽动障碍与强迫症之间的遗传关系,结果发现即便存在共享基因变异,其程度也非常有限。我们的目标是拓展当前对于囤积症、强迫症状(OCS)和终生抽动症状背后遗传结构的认识,并通过三变量分析,评估促成这些疾病病因的共同和独特遗传因素的程度。数据收集自荷兰双胞胎登记处的参与者,共5293人,来自成年同卵双胞胎(n = 2460)和异卵双胞胎(n = 2833)样本(平均年龄33.61岁)。在Mplus中对囤积症、强迫症状和抽动症状的数据进行了同时分析。对双胞胎数据拟合了一个易感性阈值模型,分析表型及其共病的遗传度。按照所有表型可能临床诊断的标准,6.8%的参与者被诊断为可能的囤积症(HD),6.3%为强迫症状,12.8%为任何可能的终生抽动障碍。遗传因素分别解释了囤积症 - 强迫症状、囤积症 - 抽动症状和强迫症状 - 抽动症状之间表型协方差的50.4%、70.1%和61.1%。在囤积症与强迫症状(0.41)、囤积症与抽动症状(0.35)以及强迫症状与抽动症状(0.37)之间观察到显著的遗传相关性。这些结果支持了遗传因素在这些疾病及其共病发展中的作用。此外,抽动症状主要受与强迫症状和囤积症不共享的特定环境因素影响。