Pharmacogenetics and the concept of individualized medicine
- PMID: 16302022
- DOI: 10.1038/sj.tpj.6500338
Pharmacogenetics and the concept of individualized medicine
Abstract
Adverse drug reaction in patients causes more than 2 million hospitalizations including 100,000 deaths per year in the United States. This adverse drug reaction could be due to multiple factors such as disease determinants, environmental and genetic factors. In order to improve the efficacy and safety and to understand the disposition and clinical consequences of drugs, two rapidly developing fields--pharmacogenetics (focus is on single genes) and pharmacogenomics (focus is on many genes)--have undertaken studies on the genetic personalization of drug response. This is because many drug responses appear to be genetically determined and the relationship between genotype and drug response may have a very valuable diagnostic value. Identification and characterization of a large number of genetic polymorphisms (biomarkers) in drug metabolizing enzymes and drug transporters in an ethnically diverse group of individuals may provide substantial knowledge about the mechanisms of inter-individual differences in drug response. However, progress in understanding complex diseases, its negative psychosocial consequences, violation of privacy or discrimination, associated cost and availability and its complexity (extensive geographic variations in genes) may become potential barriers in incorporating this pharmacogenetic data in risk assessment and treatment decisions. In addition, it requires increased enthusiasm and education in the clinical community and an understanding of pharmacogenetics itself by the lay public. Although individualized medications remain as a challenge for the future, the pharmacogenetic approach in drug development should be still continued. If it becomes a reality, it delivers benefits to improve public health and allow genetically subgroup diseases thereby avoiding adverse drug reactions (by knowing in advance who should be treated with what drug and how).
Similar articles
-
[Pharmacogenomics: the quest for individualized therapy].Rev Neurol. 2004 Dec 1-15;39(11):1063-71. Rev Neurol. 2004. PMID: 15597270 Review. Spanish.
-
Polymorphism of human cytochrome P450 enzymes and its clinical impact.Drug Metab Rev. 2009;41(2):89-295. doi: 10.1080/03602530902843483. Drug Metab Rev. 2009. PMID: 19514967 Review.
-
Genetic factors in drug metabolism.Am Fam Physician. 2008 Jun 1;77(11):1553-60. Am Fam Physician. 2008. PMID: 18581835 Review.
-
Combinatorial pharmacogenetics.Nat Rev Drug Discov. 2005 Nov;4(11):911-8. doi: 10.1038/nrd1874. Nat Rev Drug Discov. 2005. PMID: 16264434 Review.
-
[Tailor-made drug therapy].Nihon Rinsho. 2001 Jan;59(1):195-201. Nihon Rinsho. 2001. PMID: 11197856 Review. Japanese.
Cited by
-
Variants in CDA and ABCB1 are predictors of capecitabine-related adverse reactions in colorectal cancer.Oncotarget. 2015 Mar 20;6(8):6422-30. doi: 10.18632/oncotarget.3289. Oncotarget. 2015. PMID: 25691056 Free PMC article.
-
Take a look inside your eye.Croat Med J. 2008 Dec;49(6):861-3. doi: 10.3325/cmj.2008.49.861. Croat Med J. 2008. PMID: 19090613 Free PMC article. No abstract available.
-
Personalizing medicine with clinical pharmacogenetics.Genet Med. 2011 Dec;13(12):987-95. doi: 10.1097/GIM.0b013e318238b38c. Genet Med. 2011. PMID: 22095251 Free PMC article. Review.
-
Pharmacogenetics of ABCB1, CDA, DCK, GSTT1, GSTM1 and outcomes in a cohort of pediatric acute myeloid leukemia patients from Colombia.Cancer Rep (Hoboken). 2023 Mar;6(3):e1744. doi: 10.1002/cnr2.1744. Epub 2022 Oct 31. Cancer Rep (Hoboken). 2023. PMID: 36316809 Free PMC article.
-
[Influence of culture and religion on the treatment of cancer patients].Urologe A. 2019 Oct;58(10):1179-1184. doi: 10.1007/s00120-019-1003-5. Urologe A. 2019. PMID: 31338523 German.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical