Department of Clinical, Educational and Health Psychology, Division of Psychology and Language Sciences, University College London, 26 Bedford Way, London WC1H 0AP, UK.
Genome Med. 2010 Sep 20;2(9):68. doi: 10.1186/gm189.
There is heterogeneity between depression in childhood, adolescence and adulthood in terms of the gender composition of affected cases, prevalence, rates of recurrence and risk factors. This raises complex questions for refining the phenotype for molecular genetic studies of depression and the selection of appropriate proband groups. This article aims to provide a review of issues arising from family, twin and adoption studies of relevance to molecular genetic studies, and to summarize molecular genetic findings on childhood/adolescent depression. While retrospective studies of adults suggest greater familial aggregation among those with an earlier age of onset, prospective studies do not confirm this association. In fact, taken together, evidence from family and twin studies suggests that prepubertal depression is more strongly associated with psychosocial adversity, is less heritable and shows lower levels of continuity with adult depression than either adolescent or adult depression. Adolescent depressive symptoms and disorder show similar levels of heritability to depression in adult life, although there is only one twin study of adolescent depressive disorder, and heritability estimates of depressive symptoms vary widely between studies. This variability in heritability estimates is partly attributable to age and informant effects. Adoption studies and other intergenerational transmission designs show that the transmission of depression between parents and children involves genetic and environmental processes, with converging evidence that environmental processes are most important. Molecular genetic studies of childhood/adolescent depression have to date used a candidate gene approach and focused on genes already examined in adult studies. Prospective longitudinal studies of community and high-risk samples are needed to clarify issues of etiological heterogeneity in depression, and these should in turn inform the planning of molecular genetic studies.
儿童期、青春期和成年期抑郁症在患病性别构成、患病率、复发率和风险因素方面存在异质性。这为细化抑郁症分子遗传学研究的表型以及选择合适的先证者群体提出了复杂的问题。本文旨在综述与分子遗传学研究相关的来自家族、双胞胎和收养研究的问题,并总结儿童/青少年抑郁症的分子遗传学发现。虽然成人回溯性研究提示发病年龄较早的个体中家族聚集性更强,但前瞻性研究并未证实这种关联。事实上,综合家族和双胞胎研究的证据表明,青春期前抑郁症与心理社会逆境的相关性更强,遗传性较低,与成年期抑郁症的连续性也较低,而青少年或成年期抑郁症则不然。青少年抑郁症状和障碍与成年期的抑郁具有相似的遗传性,但仅有一项青少年抑郁障碍的双胞胎研究,且研究间抑郁症状的遗传性估计值差异很大。这种遗传性估计值的可变性部分归因于年龄和报告者效应。收养研究和其他代际传递设计表明,父母与子女之间抑郁症的传递涉及遗传和环境过程,越来越多的证据表明环境过程最为重要。儿童/青少年抑郁症的分子遗传学研究迄今为止采用了候选基因方法,并集中于已在成人研究中检验过的基因。需要对社区和高危样本进行前瞻性纵向研究,以阐明抑郁症病因学异质性的问题,而这反过来又应有助于规划分子遗传学研究。