Pharmacogenetics and pharmacogenomics: why is this relevant to the clinical geneticist?
- 1 October 1999
- journal article
- review article
- Published by Wiley in Clinical Genetics
- Vol. 56 (4), 247-258
- https://doi.org/10.1034/j.1399-0004.1999.560401.x
Abstract
Adverse drug reactions, due at least in part to interindividual variability in drug response, rank between the 4th and 6th leading causes of death in the USA. The field of 'pharmacogenetics', which is 'the study of variability in drug response due to heredity', should help in reducing drug-caused morbidity and mortality. The recently coined term 'pharmacogenomics' usually refers to 'the field of new drug development based on our rapidly increasing knowledge of all genes in the human genome'. However, the two terms - pharmacogenetics and pharmacogenomics - are often used interchangeably. A classification of more than five dozen pharmacogenetic differences is presented here. Most of these variations occur in drug-metabolizing enzyme (DME) genes, with some presumed to exist in the DME receptor and drug transporter genes, and others have not yet been explained on a molecular basis. A method for unequivocally defining a quantitative phenotype (drug efficacy, toxicity, etc.) is proposed; this is where help from the clinical geneticist can be especially important. Our current appreciation of the degree of variability (including single-nucleotide polymorphisms, SNPs) in the human genome is described, with emphasis on the need to prove that a particular genotype is indeed the cause of a specific phenotype; this topic has been termed 'functional genomics'. Furthermore, the current amount of admixture amongst almost all ethnic groups will obviously make studies of gene-drug interactions more complicated, as will the withholding of ethnic information about DNA samples during any molecular epidemiologic study. DME genes and DME receptor and drug transporter genes can be regarded as 'modifier genes', because they influence disorders as diverse as risk of cancer, bone marrow toxicity resulting from occupational exposure, and Parkinson's disease; for this reason, the clinical geneticist, as well as the medical genetics counselor, should be knowledgeable in the rapidly expanding fields of pharmacogenetics and pharmacogenomics.Keywords
This publication has 45 references indexed in Scilit:
- Age‐dependent genetic effects on a secondary sexual trait in male Alpine ibex,Capra ibexMolecular Ecology, 2007
- Cytoplasmic fatty acid‐binding protein facilitates fatty acid utilization by skeletal muscleActa Physiologica Scandinavica, 2003
- Genetic Variation as a Guide to Drug DevelopmentScience, 1998
- Haplotype Structure and Population Genetic Inferences from Nucleotide-Sequence Variation in Human Lipoprotein LipaseAmerican Journal of Human Genetics, 1998
- PharmacogeneticsAmerican Journal of Human Genetics, 1997
- Genomics: Structural and Functional Studies of GenomesGenomics, 1997
- Renal disease susceptibility and hypertension are under independent genetic control in the fawn-hooded ratNature Genetics, 1996
- A biometrical genome search in rats reveals the multigenic basis of blood pressure variation.Genome Research, 1995
- Genotyping for polymorphisms in xenobiotic metabolism as a predictor of disease susceptibility.Environmental Health Perspectives, 1994
- Genetic Dissection of Complex TraitsScience, 1994