Division of Human Genetics, Department of Pediatrics and Molecular Developmental Biology, University of Cincinnati Medical Center, Cincinnati, Ohio 45229, USA.
Annu Rev Pharmacol Toxicol. 2013;53:355-75. doi: 10.1146/annurev-pharmtox-011112-140241.
Genetic risk prediction uses genetic data to individualize prediction of outcome or effect from a known harmful toxicant. Several examples of toxicogenetics (usually binary traits) are discussed, reflecting largely Mendelian traits before the Human Genome Project began in 1990. Numerous complexities of the genome and what constitutes "a gene" have emerged during these past two decades. Examples of toxicogenomics (continuous outcomes, gradients) are examined. Most xenobiotic-induced environmental diseases resemble human complex diseases or other multifactorial traits such as height; these traits result from hundreds of low-effect genes. Consequently, uncovering an association between a trait and a genetic variant in a large cohort can provide important information about underlying biology; however, screening for a specific variant in an individual worker or patient has poor predictive value and little clinical utility. Individualized risk assessment for toxicants that cause environmental diseases, although a lofty goal, remains to be achieved.
遗传风险预测利用遗传数据来个性化预测已知有害物质的结果或效应。本文讨论了几个毒理学遗传学的例子(通常是二元特征),这些例子在 1990 年人类基因组计划开始之前主要反映了孟德尔特征。在过去的二十年中,基因组的许多复杂性以及什么构成了“一个基因”已经显现出来。本文还研究了毒代动力学基因组学(连续结果,梯度)的例子。大多数外源性诱导的环境疾病类似于人类复杂疾病或其他多因素特征,如身高;这些特征是由数百个低效应基因引起的。因此,在一个大型队列中发现一个特征与一个遗传变异之间的关联可以提供关于潜在生物学的重要信息;然而,在个体工人或患者中筛选特定的变异,其预测值较差,临床实用性较小。尽管个体化的环境疾病毒物风险评估是一个崇高的目标,但仍有待实现。