Ivanov Volen Z, Nordsletten Ashley, Mataix-Cols David, Serlachius Eva, Lichtenstein Paul, Lundström Sebastian, Magnusson Patrik K E, Kuja-Halkola Ralf, Rück Christian
Centre for Psychiatry Research, Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden.
Stockholm Health Care Services, Stockholm County Council, Stockholm, Sweden.
PLoS One. 2017 Jun 28;12(6):e0179541. doi: 10.1371/journal.pone.0179541. eCollection 2017.
Twin studies of hoarding symptoms indicate low to moderate heritability during adolescence and considerably higher heritability in older samples, suggesting dynamic developmental etiological effects. The aim of the current study was to estimate the relative contribution of additive genetic and environmental effects to hoarding symptoms during adolescence and young adulthood and to estimate the sources of stability and change of hoarding symptoms during adolescence.
Univariate model-fitting was conducted in three cohorts of twins aged 15 (n = 7,905), 18 (n = 2,495) and 20-28 (n = 6,218). Longitudinal analyses were conducted in a subsample of twins for which data on hoarding symptoms was available at both age 15 and 18 (n = 1,701).
Heritability estimates for hoarding symptoms at ages 15, 18 and 20-28 were 41% (95% confidence interval [CI]: 36-45%), 31% (95% CI: 22-39%) and 29% (95% CI: 24-34%) respectively. Quantitative sex-differences emerged in twins aged 15 at which point the heritability in boys was 33% (95% CI: 22-41%) and 17% (95% CI: 0-36%) in girls. Shared environmental effects played a negligible role across all samples with the exception of girls aged 15 where they accounted for a significant proportion of the variance (22%; 95% CI 6-36%). The longitudinal bivariate analyses revealed a significant phenotypic correlation of hoarding symptoms between ages 15 and 18 (0.40; 95% CI: 0.36-0.44) and a strong but imperfect genetic correlation (0.75; 95% CI: 0.57-0.94). The bivariate heritability was estimated to 65% (95% CI: 50-79%).
Hoarding symptoms are heritable from adolescence throughout young adulthood, although heritability appears to slightly decrease over time. Shared environmental effects contribute to hoarding symptoms only in girls at age 15. The stability of hoarding symptoms between ages 15 and 18 is largely explained by genetic factors, while non-shared environmental factors primarily have a time-specific effect. The findings indicate that dynamic developmental etiological effects may be operating across the life span.
囤积症状的双胞胎研究表明,在青少年时期遗传率较低至中等,而在年龄较大的样本中遗传率则高得多,这表明存在动态发展的病因学效应。本研究的目的是估计加性遗传效应和环境效应在青少年期和青年期对囤积症状的相对贡献,并估计青少年期囤积症状稳定性和变化的来源。
对年龄分别为15岁(n = 7,905)、18岁(n = 2,495)和20 - 28岁(n = 6,218)的三组双胞胎队列进行单变量模型拟合。对15岁和18岁时均有囤积症状数据的双胞胎子样本(n = 1,701)进行纵向分析。
15岁、18岁和20 - 28岁时囤积症状的遗传率估计分别为41%(95%置信区间[CI]:36 - 45%)、31%(95% CI:22 - 39%)和29%(95% CI:24 - 34%)。15岁的双胞胎出现了定量的性别差异,此时男孩的遗传率为33%(95% CI:22 - 41%),女孩为17%(95% CI:0 - 36%)。除15岁女孩外,共享环境效应在所有样本中的作用可忽略不计,15岁女孩的共享环境效应占变异的显著比例(22%;95% CI 6 - 36%)。纵向双变量分析显示年龄15岁和18岁之间囤积症状存在显著的表型相关性(0.40;95% CI:0.36 - 0.44)以及强但不完全的遗传相关性(0.75;95% CI:0.57 - 0.94)。双变量遗传率估计为65%(95% CI:50 - 79%)。
囤积症状从青少年期到整个青年期都具有遗传性,尽管遗传率似乎随时间略有下降。共享环境效应仅在15岁女孩的囤积症状中起作用。15岁和18岁之间囤积症状的稳定性在很大程度上由遗传因素解释,而非共享环境因素主要具有特定时间的效应。研究结果表明动态发展的病因学效应可能在整个生命周期中起作用。