Pgx Basic Concepts III Flashcards

1
Q

Ultrarapid Metabolizer (CYP2C19)

A

-increased activity (5-30% of patients)

Genotype:
- two increased activity alleles (17)
- one functional allele (
1) + one increased activity allele (*17)

Ex) 1/17 or 17/17

Result:
- normal or increased platelet inhibition
- normal or decreased platelet aggregation

Recommendation:
- label recommended dosage/administration

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2
Q

Extensive Metabolizer (CYP2C19)

A
  • homozygous wild type (35-50% of patients)

Genotype:
- two functional alleles (*1)

Ex) 1/1

Result:
- normal or increased platelet inhibition
- normal or decreased platelet aggregation

Recommendation:
- label recommended dosage/administration

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3
Q

Intermediate Metabolizer (CYP2C19)

A
  • heterozygote or intermediate activity (18-45% of patients

Genotype:
- one functional allele (1) + one loss of function allele (2-*8)
- one loss of function allele + one increased activity allele

Ex) 1/2 or 1/3 or 2/17

Result:
- reduced platelet inhibition
- increased platelet aggregation
- increased risk of MACE

Recommendation:
- alternative antiplatelet therapy

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4
Q

Poor Metabolizer (CYP2C19)

A
  • homozygous variant/mutant/low activity (2-15% of patients)

Genotype:
- two loss of function alleles (2-8)

Ex) 2/2 or 2/3 or 3/3

Result:
- significantly reduced platelet inhibition
- significantly increased platelet aggregation
- significantly increased risk of MACE

Recommendation:
- alternative antiplatelet therapy

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5
Q

How can a genotype determine a phenotype?

A

Change PK (effect body has on a drug)
- alters enzymatic activity during ADME
- directly leads to inter-patient difference in drug concentrations, doses, durations, etc
- inter-patient difference in toxicities and efficacies

Change PD (effect drug has on the body)
- alters drug target activity
- creates new drug target
- alters structure of protein
- change drug receptor binding

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6
Q

MAF

A

minor allele frequency

  • % are population based and can differ between populations that were analyzed or viewed
  • always testing the genotype (2N) –> combination of alleles
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7
Q

Observed Genotype Data

A
  • there is always only 3 genotypes
  • T/T or T/C or C/C
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8
Q

Formulas for MAF

A

T allele% : 2(# of ppl with homozygous T) + # of heterozygous people –> divided by 2N

C allele% : 2(# of ppl with homozygous C) + # of heterozygous people –> divided by 2N

T allele%: T genotype% + 1/2 (T/C genotype %)

C allele%: C genotype% + 1/2 (T/C genotype %)

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9
Q

Common and Rare Alleles

A
  • allele frequencies normally stay stable within a population

Common/Major/Reference Allele: frequency > 50%

Rare/Minor/Mutant Allele: frequency < 50%

A RARE ALLELE IN ONE POPULATION CAN BE A COMMON ALLELE IN ANOTHER POPULATION

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10
Q

Crossover and Recombination

A
  • occurs between homologous chromosomes during meiosis to produce gametes

Recombinant Chromosome: chromosome that is a result of crossover

Non-Recombinant Chromosome: chromosome without crossover (original)

FURTHER INCREASES THE GENETIC DIVERSITY OF A POPULATION

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11
Q

Haplotype

A
  • group of genes within an organism that were inherited together from a single parent
  • also referred to as a inheritance of a CLUSTER of SNP’s
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12
Q

Linkage Disequilibrium (LD)

A
  • non random association of alleles at different locus on the same chromosome
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13
Q

When there are infinite recombination?

A

no LD

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14
Q

When there is no recombination?

A

complete LD

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15
Q

When recombination occurs in a portion of chromosomes?

A

incomplete LD

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16
Q

Examples of LD in Pgx

A
  1. If the distance between two loci is short enough, there will be no recombination in a population
    - leads to co segregation of both loci to the next generation
    - complete LD
    - called a haplotype block
  2. If the distance between the two loci is long enough, there will be a large number of recombination between the two loci in a population
    - independent segregation of the two loci into the next generation
    - no LD
17
Q

Measures of LD

A

R2: how strong is the correlation between two variables
- measures the extent of concordance in genotypic association between two loci
- varies from 0 to 1

18
Q

R2 = 0

A

no LD

19
Q

R2 = 1

A

complete LD

20
Q

R2 ≥ 0.8

A

strong LD