genomics and precision medicine, its more than skin deep · genomics and precision medicine as the...
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Genomics and Precision Medicine, Its More than
Skin Deep
• DeShana Collett, MSPAS, PA‐C, PhD
• Susan LeLacheur, DrPH, PA‐C
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Objectives
Describe advances and gaps in clinical applications of precision medicine.
1Discuss dilemmas in teaching physician assistants about genomics and precision medicine as the scientific, legal and ethical context rapidly changes.
2Describe ways of teaching students to incorporate modern understanding of genomics along with social, behavioral and environmental factors into personalized care for the patient.
3
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What is Precision and Personalized Medicine?
The current landscape and impact of precision medicine on the four (4) P's
Predictive Analytics• Artificial Intelligence• Big Data, Deep Learning IntelligencePersonalization• GenomicsPrevention
Participatory
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Human Genome Project and the Precision Medicine Initiative
This Photo by Unknown author is licensed under CC BY‐NC‐ND.This Photo by Unknown author is licensed under CC BY‐ND.
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What is includedWhat is
Artificial Intelligence Genomics Pharmacogenetics
GlobalMetabolomics Assessment
Microbiome testing
EMR System Intergrations
Research: Undiagnosed Disease Network
Education: Future and Current Healthcare workforce
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Current State of Precision Medicine
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Clinical Applications
Advil
Cut
DIE
Ibuprofen
This Photo by Unknown author is licensed under CC BY.
Never
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Genetic Testing
Predictive
Diagnostic
Pharmacogenetic
Screening: Carrier, Prenatal,
Newborn
Preimplantation
DTC
Forensic
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Human Genomic Sequencing: What is all the hype about!
• Genotype Testing• Direct To Consumer (DTC)
• Whole Exome Sequencing
• Whole Genome Sequencing
This Photo by Unknown author is licensed under CC BY‐NC.
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Pharmacogenetics
•Opioid Crisis= What about pharmacogenomics ?•CYP2D6= Codeine, Tramadol. CPIC guidelines 2014• Anti‐depressants?•CYP2D6& CYP2C19= CPIC guidelines SSRI, 2015, TCA(2016),•Others through CYP2D6& CYP2C19= : Ondansetron (2017) Tamoxifen (2018)•Warfarin metabolism!!!= CYP2C9,VKOR1, CYP4F2, rs12777823
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• Clinical instruments• Sequencing• Analysis
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Direct‐ To Consumer Test and Consumer Controlled Market
• Direct to Consumer • Consumer Controlled Consent
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Nutrigenomics
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HealthCare System Integrations
Geisinger Health
Humanwide Project
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No more "One Size Fits All" Approach
©2019 Forbes Media LLC. All Rights Reserved
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Author: Joe Heller (2000)
Key Clinical Ethics Concerns
• The capacity to act on your own decisions freely and independently• Respect a patient’s dignity/rt to make decisions• (What is adequate Informed Consent to genetic testing?)
Autonomy
• Treating patients fairly and equitably • (How do we ensure that all patients are treated fairly?)
Justice
Beneficence/Non‐maleficence
• Risk/Benefit Analysis• (How do we engage in genetic testing responsibly?)
First do no harm
• (What are the limits to these duties?)
Privacy/Confidentiality
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Autonomy
• At what age is an individual competent to consent?• Should newborns be given a chance to decide later in life?
• Do family members have a right to know a relative’s genetic test result?
• What if a patient does not want to know genetic test results? (long term probabilistic vs. lifesaving knowledge)
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Do No Harm
• Testing• When do we provide testing?• How do we prevent the use of unnecessary procedures?
• Counseling• How do we provide genetic/genomic information responsibly?• Psychological harms
• When do we provide counseling?• Some proteins reveal genetic risk–counsel before or after protein testing?
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Molly Nash, 6, receives a stem cell transplant from her IVF conceived brother who was tested for HLA compatibility, 2007
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Fairness
Is it possible to treat patients fairly when some patients have variants of unknown significance?
Why do some doctors order genetic tests for African‐American women at lower rates?
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Diversity & Inclusion96% of participants in genome‐wide association studies of European descent (2009)Participants of Asian ancestry increased to 20%African American and Latino participation under 4%
Population descriptors• 'black cases' and 'sub‐Saharan African', were
often used to describe people of African ancestry.
• More often “geographically specific and informative descriptions were those used for samples of European origin. . .”
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Self‐perpetuating Bias
Ferryman K & Pitcan M. Fairness in Precision Medicine, Data & Society 2018 https://datasociety.net/wp‐content/uploads/2018/02/Data.Society.Fairness.In_.Precision.Medicine.Feb2018.FINAL‐2.26.18.pdf
Bias in Datasets: datasets can become unintentionally biased through a) a lack of cohort diversity, b) technical processes of data collection and cleaning, and c) the
specific incorporation of electronic health record data.
Bias in Outcomes: the outcomes of precision medicine research can be discriminatory in many ways. These include a) too much focus on individual responsibility for health, b) the marginalization of those population groups
with lower health literacy or in less resourced areas, and c) the potential to shift the accepted forms of biomedical research.
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Mersha, T. B., & Abebe, T. (2015). Self‐reported race/ethnicity in the age of genomic research: its potential impact on understanding health disparities. Hum Genomics, 9, 1.
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Mersha TB & Abebe T, Human Genomics 2015
“One of the great truths to emerge from this triumphant expedition inside the human genome is that in genetic terms, all human beings, regardless of race, are more than 99.9 percent the same.”
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Scholz v. Kaiser Foundation Hospital, RG12614636,Alameda Sup. Ct. (filed Jan. 30, 2012)
Payne PW, Jr. Journal of Law, Medicine and Ethics, 2008
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Privacy/Confidentiality
• The interest of others• Public or Employer Interest
• Examples• Eddie Curry and Ryan Clark• Fatal heart condition
• Sickle cell trait• Employee DNA testing
• Prohibited by GINA
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Ethical Recommendations
Foreseeable, identifiable victim & serious risk
TARASOFF v. THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
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Ethical Recommendations
• A clinician’s duty may be fulfilled by encouraging patients to communicate with relatives ‐ American Society of Clinical Oncology, 2010
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Ethical Recommendations • Should the physician have a duty to find and notify relatives?
• The AMA Code of Medical Ethics, Opinion 2.131 (Based on 2003 Report)• Finding and notifying family members is not a physician’s duty
• Physicians should inform patients in advance of what they expect them to disclose to their families and be available to assist in this communication
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Ethical RecommendationsThe Committee on Genetic Risks of the Institute of Medicine (1994)• Confidentiality may be breached, and the relatives informed of the risks when:
• Attempts to elicit voluntary disclosure fail• There is a high probability of irreversible or fatal harm to the relative• The disclosure of the information will prevent harm• The disclosure is limited to the information necessary for diagnosis or treatment of the relative
• There is no other way to avert harm
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Law
• Example questions• Can you be sued for malpractice for failing to order a genetic test?
• What is the legal standard for ordering genetic testing services?
• What is the legal standard for following drug label guidance?
• What is the legal standard for discussing genetic test results with patients?
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Can you be sued for medical malpractice?
• Failure to diagnose, interpret, offer, disclose
• Examples• Negligent delivery of a newborn• Failure to completely review the medical record • Failure to order a genetic test or refer to a specialist • Adverse drug reactions• Unsuccessful tumor treatment
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Keel v. Banach (Ala. 1993)
• Duty to perform standard of care to patient• Prudent care /custom, lit, state of the science?
• SOC Breach • Failed to detect risk of abnormality before or
during pregnancy.
• Causation• Proximate cause: negligently performed or
omitted counseling, prenatal testing lack of informed decision re conception
• Court: Parents may maintain action for wrongful birth if the result of negligent failure of the attending prenatal physician to discover and inform them of the existence of fetal defects.
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Molloy v. Meier (Minn. 2004)• Medical Negligence (Wrongful Conception)
• Facts• failure to diagnose Fragile X in 1st daughter (with ex husband) 2nd child, son
• Pediatrician noticed developmental delays; tests failed to reveal source; reasonable to test for Fragile X but excluded –general report negative. • Series of Drs failed to diagnose, incl neurologists (Dr. Backus & Green)
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Molloy v. Meier (Minn. 2004)
• Expert testimony: pediatrician and pediatric neurologist• The prevailing standard of care in the medical community with respect to testing and counseling for genetic disorders is that if patient exhibits the symptoms of Fragile X and has a family history of mental disability –patient should be tested for Fragile X
• Physician has additional duties to (a) follow up to confirm that the tests are performed and (b) provide genetic counseling to child’s family.
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Molloy v. Meier (Minn. 2004)
• Plaintiffs argue on Appeal• Duty arising from Dr‐patient relationship• Requires warning mother about pregnancy risks as carrier of Fragile X.
• Foreseeability of injury requires Dr. to warn others of a patient’s genetic disorder (i.e. 3rd party family members)
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Additional Legal Considerations • Negligence (Duty, breach of duty, injury,
causation)• Professional Guidance• Statutes/Regulations• Cases
• Health Insurance Portability & Accountability Act (HIPAA)
• Family Educational Rights and Privacy Act (FERPA)
• GINA versus the American with Disabilities Act (ADA)• When does a genetic mutation become a disability?
• Insurance only covers disabilities & disease
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Application to Physician Assistants
What will hold up in Court?
• Providing an “ordinary standard of care”, which• Includes the highest possible degree of vigilance, prudence, and thoughtfulness.
• Evidence that patient was warned. • Evidence of consultation with specialist.
When is it too soon to test?
• Is there enough clinical evidence?• Standard in the field?• Are there other equally efficient methods that can be employed?
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Emerging Concerns
• Early adoption by consumers (Patient Right to know?)
• Blurred lines between research and discovery (i.e., genomic incidental findings)
Callier, S. 2015
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I don't want people having
my DNA!!!
• 60% of American with European Descent can be identified through DTC testing companies( Erlich, Yaniv, Tal Shor, Itsik Pe'er, and Shai Carmi. "Identity Inference of Genomic Data Using Long‐range Familial Searches." Science (New York, N.Y.) 362.6415 (2018): 690‐94. Web)• Even if you never tested you are likely to be identified through cross referencing of anonymized DNA data with public datasets!
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Genetic Information Nondiscrimination Act. of
2008: GINA
• Protects against discrimination based on genetic information.• Employment• Health Insurance
• Does not protect discrimination with• Life, long‐term, or disability insurance
• Health benefits of military and federal government employees,
• Benefits of Veterans Health , or Indian Health Service
This Photo by Unknown author is licensed under CC BY‐NC‐ND.
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GedMatch and CODIS
• Read Terms of Service for use• Gedmatch= 2010 public gedcom DNA matching software. No terms of service initially. Opt‐out is the default. ( rapes, murders, FBI‐Violent crimes and unidentified bodies
• Gives information if you match any of the Law Enforcement kits.
Combined DNA Index System (CODIS)
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Clinical Practice Guidelines
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Teaching PA Students
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Future for how we educate
Education will be at a more complex molecular and biological level
Critical analysis of genomic and computational literature
Guidance on how to effectively integrate emerging precision medicine with current evidence‐based medicine.
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References
• Banda, Y., Kvale, M.N., Hoffmann, T.J., Hesselson, S.E., Ranatunga, D., Tang, H., Sabatti, C., Croen, L.A., Dispensa, B.P., et al., 2015. Characterizing Race/Ethnicity and Genetic Ancestry for 100,000 Subjects in the Genetic Epidemiology Research on Adult Health and Aging (GERA) Cohort. Genetics 200:1285‐95.
• Bonham, V.L., Green, E.D., Pérez‐Stable, E.J., 2018. Examining How Race, Ethnicity, and Ancestry Data Are Used in Biomedical Research. JAMA 320:1533‐34.
• Bonham, V.L., Sellers, S.L., Woolford, S.J.B.H.S.R., 2014. Physicians’ knowledge, beliefs, and use of race and human genetic variation: new measures and insights. 14:456.
• Dunseath, S., Weibel, N., Bloss, C.S., Nebeker, C., 2018a. NIH support of mobile, imaging, pervasive sensing, social media and location tracking (MISST) research: laying the foundation to examine research ethics in the digital age. NPJ digital medicine 1:20171.
• Erlich, Y., Shor, T., Pe'Er, I., Carmi, S., 2018. Identity inference of genomic data using long‐range familial searches. Science (New York, N.Y.) 362:690‐94.
• Ferryman K & Pitcan M. Fairness in Precision Medicine, Data & Society 2018 https://datasociety.net/wp‐content/uploads/2018/02/Data.Society.Fairness.In_.Precision.Medicine.Feb2018.FINAL‐2.26.18.pdf
• Guttmacher, A.E., Collins, F.S., 2002. Genomic Medicine — A Primer. New England Journal of Medicine 347:1512‐20.
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References
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