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University of Utah Department of Human Genetics Pharmacogenomic s Louisa A. Stark, Ph.D. Director

University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

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Page 1: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

University of UtahDepartment of Human Genetics

PharmacogenomicsLouisa A. Stark,

Ph.D. Director

Page 2: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

Adverse drug reactions

• Every year, over 106,000 people in the United States die from adverse reactions to correctly prescribed doses of drugs.

• Another 2.2 million suffer serious, but not deadly, side effects.

A major health issue

Page 3: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

• 4th leading cause of death in the U.S.• 15% of U.S. hospital admissions• $136 billion in medical costs (2001)

• 80-85% of drug response is due to genetics

Adverse drug reactions

A major health issue

Page 4: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

• First emerged around the 1950’s

• Scientists began to notice that different responses to drugs ran in families and ethnic groups.

Field of pharmacogenetics

Page 5: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

Tour of the Basics

DNA: The basis of genetics

DNACell

Chromosomes

Page 6: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

• We are all 99.9% similar in our DNA. • Individuals vary by only 0.1%

• Individual variations may correlate with different responses to medicines and magnitude of disease risk.

Human Genome Project data

Page 7: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director
Page 8: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

Pharmacogenetics

Page 9: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

Goal of pharmacogenetics

Page 11: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

• Break down more than 30 classes of drugs– Beta-blockers, tricyclic

antidepressants, morphine derivates, antiarrhythmics, etc.

• Poor metabolizers – need lower dose– 6% of Caucasians– 2% of African Americans– 1% of Asians

• Ultra-rapid metabolizers – need higher dose– 20% of Ethiopians– 7% of Spanish– 1.5% of Scandinavians

Liver enzymes

Page 12: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

Pharmacogenetics today: leukemia

Chemotherapy for leukemia

Page 13: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

• 5-flurouracil (5-FU)- Chemotherapy agent- Stops tumor formation- Used to treat colorectal, breast, lung, cervical,

neck and head cancer- Effective for 20-30% of patients with colorectal

cancer- Genotype predicts treatment effectiveness

- Patients with 1 genotype are 5 times more likely to respond successfully to treatment with 5-FU than patients with another genotype

Pharmacogenetics today: cancer

Page 14: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

• 4 major statin drugs for lowering cholesterol

• Clinical trial looking for genetic associations in patient response to each drug

• Of 10,000 people in Iceland taking statins, 2,000 do not respond and are related to each other

Pharmacogenetics today: cholesterol

Page 15: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

Future applications: depression

• Three high school students, Marti, Toni, and Brianna, sought treatment for depression. Their doctor prescribed nortriptyline, a common antidepressant medication.

• After taking the medication for a month, Marti felt much better. She had few episodes of depression and no adverse reactions to the drug.

• Toni's depression also had subsided. However, she could not sleep and often felt nauseated and anxious.

• The medication didn't do much for Brianna: she felt neither better nor worse and had no adverse reactions to the drug.

Page 16: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

Gene expression

Page 17: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

Gene expression: application to obesity

Page 18: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

• Create diagnostic tests to predict whether a patient has a genetic predisposition to obesity. – Examine the DNA sequence of a person's obesity-related

genes to detect genetic signatures that predict a predisposition to obesity.

– Examine a tissue sample for abnormal gene expression patterns that indicate a predisposition to obesity.

• Design drugs intended to treat or prevent

obesity. – Develop drugs that inhibit the function of proteins related to

obesity.

• Design drugs to control expression of obesity genes.– Drugs would interact directly with DNA in key cells and tissues

to prevent genes from being turned on or off.

Gene expression: application to obesity

Page 19: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

• People vary in their risk of getting certain diseases.

• Example:– Two 15-year-old boys are the

same height and weight, with similar diet and exercise habits.

– Determine risk for developing diabetes.

Determining disease risk

Page 20: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

• New, more accurate diagnostic tests– Predict a patient's response to

specific drugs based on his or her genetic profile.

Benefits of pharmacogenetics

•Personalized drug therapies–Match a patient with effective and safe medications based on information from diagnostic tests.

•Personalized disease prevention strategies

–Developed using genetic tests that estimate a patient's risk of getting a particular disease, combined with personalized drug therapies.

Page 21: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

Pharmacogenetics: public health issues

• Population-based screening tests- How will we weigh the medical and economic

benefits of genotyping all individuals in order to direct an intervention to only a few?

- Example: Women with the factor V Leiden allele who use oral contraceptives are at greatly increased risk of venous thrombosis. Should all women be tested for this allele before beginning to take oral contraceptives?

Page 22: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

Issues related to pharmacogenetics

• Drug development for less-common SNP profiles- Who will pay for development of less profitable drugs?

• Insurance and Medicaid coverage - Will potentially expensive diagnostic tests be covered?

• Education of health care providers - How will providers be trained to understand new

diagnostic tests and use them when treating and advising patients?

• Ethical and privacy issues- Who will have access to genetic information and

databases? - How do families handle conflicts when one person

wants to be tested and others do not?- Should parents decide whether their children should be

tested?

Page 23: University of Utah Department of Human Genetics Pharmacogenomics Louisa A. Stark, Ph.D. Director

Genetic Science Learning Center Website

http://gslc.genetics.utah.eduhttp://gslc.genetics.utah.edu

To learn more about pharmacogenomics

Scientific

American.co

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