Pembrey Marcus
Institute of Child Health, University College London, London, UK.
Eur J Endocrinol. 2004 Nov;151 Suppl 3:U125-9. doi: 10.1530/eje.0.151u125.
The Avon Longitudinal Study of Parents and Children (ALSPAC) has collected detailed phenotypic and environmental information from pregnancy onwards on approximately 14 000 babies born in 1991-1992. A DNA bank on over 10 000 mothers and children has been established with generic consent for (undisclosed) genetic analysis, and cell lines on both children and parents are planned. As a multigenerational population cohort unselected by disease, trait or exposure, ALSPAC is uniquely placed to explore the genetic and environmental determinants of adverse developmental responses and common disease. Added value for genetic epidemiology generally is the ability to detect distortion of the expected Mendelian 50:50 transmission of alleles to study subjects (e.g. due to differential loss of embryos of one genotype) or to test for heterosis, i.e. whether heterozygotes have a greater or lesser effect than either homozygote. Finally, phenome scans (a fixed format analysis of the associations between a genotype of interest and thousands of outcome variables from the cohort database) could be used as a screening tool to test whether certain classes of genetic variation have more impact than others on human health and development.
雅芳亲子纵向研究(ALSPAC)从怀孕起就收集了约14000名1991年至1992年出生婴儿的详细表型和环境信息。已建立了一个包含10000多名母亲和儿童的DNA库,并获得了进行(未公开的)基因分析的一般同意,同时计划建立儿童和父母的细胞系。作为一个未因疾病、性状或暴露而进行选择的多代人群队列,ALSPAC在探索不良发育反应和常见疾病的遗传和环境决定因素方面具有独特的地位。遗传流行病学的附加价值通常在于能够检测等位基因向研究对象的预期孟德尔50:50传递的扭曲情况(例如,由于一种基因型胚胎的差异性丢失),或者测试杂种优势,即杂合子的效应是否比任何一种纯合子更大或更小。最后,表型组扫描(对感兴趣的基因型与队列数据库中的数千个结果变量之间的关联进行固定格式分析)可以用作一种筛选工具,以测试某些类别的基因变异对人类健康和发育的影响是否比其他变异更大。