Personalized Medicine And Pharmacogenomics Flashcards
Personalized medicine
In drug therapy, idiopathic disease, cancer, prenatal testing and newborn screening
Number of genes present is not directly correlated with complexity of organisms
Humans have 20,500 genes which is only slightly larger than number of genes of zebra fish
DNA sequences of 2 individuals are 99.5% identical
Pharmacogenetics
Pharmacogenomics
Pharmacogenetics: this relates heritable variation to inter-individual variation in drug response
Pharmacogenomics: the field of new drug development based on our rapidly increasing knowledge of all genes in the human genome
Drug design influenced by genetics, adverse drug reaction results in FDA rejection of drug
Cytochrome P450
Gene family that includes a variety of different enzymes involved in drug metabolism (as well as lipids and hormones)
Mutations in genes result in a change in enzyme’s ability to perform its function
One member of family’s genotype affects ability to metabolize certain drugs: CYP2D6
Classes of function
Extensive (normal condition): presence of two functional alleles that work expectedly, most drugs are targeted towards these individuals
Poor metabolizer: nonfunctional allele, difficulty converting drugs to useable forms, accumulation of chemicals in body, toxic, require lower dosage of drug
Ultra metabolizer: duplicate copies of functional alleles, degrades drug rapidly, higher doses or other drugs to be more effective
Intermediate metabolizers: heterozygous with one functional and one mutant allele, can utilize drug but at a slower rate, need lower than normal dose
Warfarin
Coumadin is anticoagulant
Synthesis form of drug is warfarin
Useful in rodent poisons, but when used properly can prevent inappropriate thrombosis
React with common medicines, foods with a lot of vit k, excessive alcohol
Vitamin K essential for function of many clotting factors, functional cofactors only work if reduced from of vit K can be converted to oxidized form, oxidized vit K then changed back to reduced form by enzyme vit k reductase (VKOR), warfarin inhibits VKOR which limits cofactors, results in loss of ability to coagulate blood
VKORC1 allele of VKOR gene and CYP2C9 allele of cyt p450 directly affect warfarin metabolism
Microarray
Allow genome wide scan of an individual’s genetic complement
Information could be obtained on an individual’s mutational status for selected genes, used to manage patient’s health throughout life
Problem if individual doesn’t want to know this information
Regions of homozygosity (ROH)
When Intermediate sized ROH are seen, could be due to identity by descent which occurs in inbred populations, isolated populations or specific ethnic groups
Increases likelihood of expression of recessive disorder
Genetic information nondiscrimation act (GINA)
Enacted to prevent genetic discrimination when genetic information is available
Fear that people will lose insurance coverage and job opportunities if companies became aware of genetic diagnosis
Personalized medicine in Screening
Prenatal screening
Newborn screening tests newborns for a defined set of genetic diseases
Carrier screening looks at individuals who are phenotypically normal but who may be at risk of having an affected child if their partner is also a mutation carrier for disease