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Printable Handouts
Navigable Slide Index
- Introduction
- Personalized medicine
- Manners for individualized therapy
- Adverse drug reactions (ADRs)
- Increased incidence in ADRs
- Causes of ADRs
- Drug metabolism and excretion
- Drugs metabolized by P450 isoforms
- Route of elimination for top prescribed drugs
- Genetic drift and genetic selection
- Evolution of human P450 genes
- Evolution of CYP2D6 in mice and humans
- Forest experiment
- Insect selection based on P450 gene inducibility
- Shift of host by insects
- The human situation: starting in Ethiopia
- Duplicated & multiduplicated CYP2D6*2 genes
- Global distribution of duplicated CYP2D6 alleles
- Adaptation to the environment among CYPs
- Dietary stress induced CYP2D6 gene duplications
- Pharmacogenomic biomarkers
- CYP2C19 genotype and clopidogrel treatment
- Drug treatment affected by DME polymorphism
- Some consequences of CYP gene polymorphism
- Warfarin- pharmacokinetics & pharmacodynamics
- Warfarin treatment in genotyped patients
- Rare alleles
- Whole exome sequencing based analyses of CYP
- CYP gene distribution
- World distribution of CYP SNVs
- Rare mutations in CYP gene family- conclusions
- Transport, metabolism & elimination of taxanes
- CYP3A4 polymorphism is very rare in general
- Impact of CYP3A4 variants (neuropathy, treatment)
- Every individual has his/her relevant SNPs
- Genetic variability and cancer treatment
- Polymorphisms may affect breast cancer patients
- Pharmacogenomic labels
- Pharmacogenomic biomarkers in drug labels
- FDA list-cancer pharmacogenomic biomarkers (1)
- FDA list-cancer pharmacogenomic biomarkers (2)
- FDA list-cancer pharmacogenomic biomarkers (3)
- EMA pharmacogenomic labels in SmPCs
- Conclusions
Topics Covered
- Pharmacogenomics and adverse drug reactions
- Evolutionary basis of pharmacogenomics and interethnic differences
- Deletion, duplication, multiduplication or amplification of active P450 genes
- Importance of polymorphism of drug metabolizing genes and drug targets for drug therapy
- The importance of rare mutations for precision medicine
- Drug pharmacogenomics labels and their clinical use
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Ingelman-Sundberg, M. (2016, August 31). Pharmacogenomics [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 21, 2024, from https://doi.org/10.69645/IONZ5423.Export Citation (RIS)
Publication History
Financial Disclosures
- He is the co-founder and co-owner of HepaPredict AB.
A selection of talks on Biochemistry
Transcript
Please wait while the transcript is being prepared...
0:00
Hello!
My name is
Magnus Ingelman-Sundberg.
I am a professor
at the Karolinska Institutet
in Stockholm, Sweden.
And I will talk to you
about Pharmacogenomics.
0:12
The personalized
medicine era is coming,
and it's very important
to individualize the drug therapy
to comply with the genetics
and the conditions
of the individual patient.
The most important variables
to take into consideration
are the genetic variation
where genes encoding,
drug metabolism,
drug transport, and drug targets
vary between individuals.
By knowing the differences
between two individuals
in the gene composition,
we can adjust the drug dosage
and the choice of the drug
to comply with the requisites
by the patient in question.
Other parts
of the personalized medicine
to take into consideration
are the epigenetic variation,
also which is very important
is drug interactions.
People taking many drugs
simultaneously
cannot be aware of that
they interact with each other
and make complications
in the drug treatment.
An example of that is exerted by
adverse drug reactions.
Personalized medicine
has also to take into account
the health factors of the patient,
particular pathophysiology,
the patient's BMI,
the age, the lifestyle.
The gender is not very important
for drug therapy differences.
And there are some differences,
but they are not as large
as the other variables
that are important for
personalized medicine.
To monitor the changes
and the situation
in a particular patient,
we can take biomarkers
from blood, tissues, etc...
and measure somatic mutations
coming from the tumors
or other kinds of
circulating biomarkers
that give us a view
of the situation in the patient.