Genetic Risk Prediction: Individualized Variability in Susceptibility to Toxicants

被引:13
|
作者
Nebert, Daniel W. [1 ,2 ,3 ]
Zhang, Ge [1 ]
Vesell, Elliot S. [4 ]
机构
[1] Univ Cincinnati, Med Ctr, Div Human Genet, Dept Pediat & Mol Dev Biol, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Med Ctr, Dept Environm Hlth, Cincinnati, OH 45229 USA
[3] Univ Cincinnati, Med Ctr, Ctr Environm Genet, Cincinnati, OH 45229 USA
[4] Penn State Univ, Dept Pharmacol, Coll Med, Hershey, PA 17033 USA
来源
ANNUAL REVIEW OF PHARMACOLOGY AND TOXICOLOGY, VOL 53, 2013 | 2013年 / 53卷
关键词
environmental genetics; epigenetics; genetic risk prediction; genome-wide association studies; Mendelian trait; multifactorial trait; toxicogenetics; toxicogenomics; GENOME-WIDE ASSOCIATION; ARYL-HYDROCARBON RECEPTOR; DNA METHYLATION PATTERNS; COMPLEX TRAITS; MISSING HERITABILITY; ROC CURVE; CYP1A2; GENOTYPE; HUMAN-DISEASES; COMMON SNPS; EXPRESSION;
D O I
10.1146/annurev-pharmtox-011112-140241
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:355 / +
页数:28
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