Direct-to-Consumer Genetic Testing Developed by Dr. June Carroll, Ms. Shawna Morrison and Dr. Judith Allanson Last updated April 2014.

Slides:



Advertisements
Similar presentations
PERSONALIZED MEDICINE: Planning for the Future You, Your Biomarkers and Your Rights.
Advertisements

Taking Research and Development to the Clinic: Issues for Physicians AAAS/FDLI Colloquium I Diagnostics and Diagnoses Paths to Personalized Medicine Howard.
Genetics and genomics for healthcare © 2014 NHS National Genetics and Genomics Education Centre Why is genetics relevant to.
ROSALIND CHUANG, M.D. DEPARTMENT OF NEUROLOGY STANFORD UNIVERSITY Informed consent for genetic testing: Genetics 210.
The views and statements expressed here are provided for informational purposes and do not necessarily reflect those of Medivo, the Alliance for Continuing.
Alzheimer disease Developed by Dr. June Carroll, Ms. Shawna Morrison and Dr. Judith Allanson Last updated April 2015.
Hereditary Factors in Breast Cancer
GenetiKit Workshop Given by: Dr. Sean Blaine, Family Physician Dr. June Carroll, Family Physician Clare Gibbons, Genetic Counsellor Cathy Gilpin, Genetic.
Breast Cancer Risk and Risk Assessment Models
Direct to Consumer Testing Issues. Types of tests being sold Diagnostic tests – identify specific conditions Carrier testing - identify those who carry.
19th century20th century 21st century (Flemming, 1882) Where is genetics headed?
Why Are We Here? The History and Landscape of DTC Genetic Tests Elizabeth Mansfield, Ph.D. OIVD/CDRH/FDA March 8, 2011 Molecular and Clinical Genetics.
Human Genetics Overview.
Clinical Applications of Whole Genome/Whole Exome Sequencing Robert L. Nussbaum, MD, FACMG Division of Genomic Medicine, UCSF AMA – November 11, 2012.
By Dr. Ahmed Mostafa Assist. Prof. of anesthesia & I.C.U. Evidence-based medicine.
Prescreening ä To optimize safety ä To permit the development of a sound and effective exercise prescription.
Alcohol & other addictions: can DNA make a difference? Dr Martin Kennedy Department of Pathology Christchurch School of Medicine & Health Sciences University.
EVIDENCE-BASED PRACTICE
What is personal genetics? What might it mean for me, my family and society? Personal Genetics Education Project (pgEd) Harvard Medical School
Breast Screening. NHS Breast Screening Programme Introduced in 1988 Invites women from age group for screening every 3 yrs. Age extension roll-out.
Are exposures associated with disease?
Genomics Alexandra Hayes. Genomics is the study of all the genes in a person, as well as the interactions of those genes with each other and a person’s.
Copyright © 2010 Pearson Education, Inc. publishing as Benjamin Cummings Lectures by Greg Podgorski, Utah State University Diet Advice From DNA? Current.
Multiple Sclerosis Developed by Dr. June Carroll, Ms. Shawna Morrison, Dr. Judith Allanson Last updated Dec 2014.
Georgia Wiesner, MD CREC June 20, GATACAATGCATCATATG TATCAGATGCAATATATC ATTGTATCATGTATCATG TATCATGTATCATGTATC ATGTATCATGTCTCCAGA TGCTATGGATCTTATGTA.
Multiple Choice Questions for discussion
Epigenome 1. 2 Background: GWAS Genome-Wide Association Studies 3.
Multiple Sclerosis Developed by Dr. June Carroll, Ms. Shawna Morrison, Dr. Judith Allanson Last updated April 2015.
Chapter 13 Carrier Screening. Introduction Carrier screening involves testing of individuals for heterozygosity for genes that would produce significant.
Privacy risks of direct to consumer genetic testing Emily Christofides and Kieran O’Doherty University of Guelph OPC Contributions Grant
SHAWN KISE, BSN, RN May 14 th 2012 Wright State University CVD IN MIDDLE AGE MEN.
What is personal genetics? What might it mean for me, my family and society? What is personal genetics? What might it mean for me, my family and society?
Personalized Medicine The Promise of the Genomic Revolution.
Center for Tobacco Research and Intervention University of Wisconsin Medical School Transdisciplinary Tobacco Use Research Centers Linking Together to.
Your genome: What does your DNA say about you? Personal Genetics Education Project (pgEd) Harvard Medical School personal genetics education.
Personalized Medicine Dr. M. Jawad Hassan. Personalized Medicine Human Genome and SNPs What is personalized medicine? Pharmacogenetics Case study – warfarin.
1 Risk Assessment Tests Marina Kondratovich, Ph.D. OIVD/CDRH/FDA March 9, 2011 Molecular and Clinical Genetics Panel for Direct-to-Consumer (DTC) Genetic.
Evidence-Based Medicine – Definitions and Applications 1 Component 2 / Unit 5 Health IT Workforce Curriculum Version 1.0 /Fall 2010.
Risk Prediction of Complex Disease David Evans. Genetic Testing and Personalized Medicine Is this possible also in complex diseases? Predictive testing.
Direct-To-Consumer Genetic Testing Developed by Dr. Judith Allanson, Ms. Shawna Morrison and Dr. June Carroll Last updated November 2015.
Private pay, physician ordered genetic testing Developed by Dr. Judith Allanson, Ms. Shawna Morrison and Dr. June Carroll Last updated November 2015.
Consanguinity Developed by Dr. Judith Allanson, Ms. Shawna Morrison and Dr. June Carroll Last updated November 2015.
Smoking and Mental Health Problems in Treatment-Seeking University Students Eric Heiligenstein, M.D. University of Wisconsin-Madison Health Services Stevens.
Nursing research provides the foundation for EVIDENCE-BASED NURSING PRACTICE.
Alzheimer disease Developed by Dr. June Carroll, Ms. Shawna Morrison and Dr. Judith Allanson Last updated Dec 2014.
Analytical Studies Case – Control Studies By Dr. Sameh Zaytoun (MBBch, DPH, DM, FRCP(Manch), DTM&H(UK),Dr.PH) University of Alexandria - Egypt Consultant.
What’s the Big Deal? Andrea Sport Health Promotion Project Presentation.
Ethics in Clinical Genetics and Genomics Key Knowledge Year 4 Medical Ethics and Law Thread Course, The Ethox Centre, University of Oxford.
EMGO Institute for Health and Care Research Quality of Care Martina Cornel Professor of Community Genetics & Public Health Genomics Genomics in health.
Making Every Contact Count (MECC) and Optimising Outcomes Dr Siân Griffiths Consultant in Public Health Medicine.
Direct-to-Consumer Genetic Testing: Outputs from the EASAC-FEAM Working Group Martina Cornel VU University Medical Center, Amsterdam.
Direct-to-Consumer Genetic Testing Developed by Ms. Shawna Morrison, Dr. June Carroll, and Dr. Judith Allanson Last updated May 2016.
Chapter 7: Epidemiology of Chronic Diseases. “The Change You Like to See….” (1 of 3) Chronic diseases result from prolongation of acute illness. – With.
Self-pay, expanded carrier screening Developed by Ms. Shawna Morrison, Dr. June Carroll, and Dr. Judith Allanson Last updated May 2016.
Next generation genomics: translation into clinically useful applications in health care Prof.dr. Martina Cornel
1 Finding disease genes: A challenge for Medicine, Mathematics and Computer Science Andrew Collins, Professor of Genetic Epidemiology and Bioinformatics.
CoRPS London 26 & 27 October 2010 Center of Research on Psychology in Somatic diseases Understanding PRO in hematological disorders: Do we have a consensus?
What are some benefits, risks and limitations of genetic testing?
How Do We Individualize Guidelines in an Era of Personalized Medicine? Douglas K. Owens, MD, MS VA Palo Alto Health Care System Stanford University, Stanford.
Hereditary Cancer Predisposition: Updates in Genetic Testing
Multiple Sclerosis Developed by Dr. June Carroll, Ms. Shawna Morrison, Dr. Judith Allanson Last updated April 2015.
Expanded carrier screening
Introduction to Direct-to-Consumer Genetic Testing
EVIDENCE-BASED PRACTICE
Chapter 5: Genetics and genomics perspectives in nursing
WHY GENETIC COUNSELING IS IMPORTANT
Genetic Testing Result Means. Before Genetic Testing  The result of genetic testing can be life changing.  It is important for patients and their families.
Six W’s of Genetic Testing
Family History to Promote Individual Health
Presentation transcript:

Direct-to-Consumer Genetic Testing Developed by Dr. June Carroll, Ms. Shawna Morrison and Dr. Judith Allanson Last updated April 2014

Disclaimer This presentation is for educational purposes only and should not be used as a substitute for clinical judgement. GEC-KO aims to aid the practicing clinician by providing informed opinions regarding genetic services that have been developed in a rigorous and evidence-based manner. Physicians must use their own clinical judgement in addition to published articles and the information presented herein. GEC-KO assumes no responsibility or liability resulting from the use of information contained herein.

Objectives Following this session the learner will be able to: – Discuss and address patient concerns regarding direct-to- consumer genetic testing – Find high quality genomics educational resources appropriate for primary care

Case Jim, 53yo male Healthy, active, non-smoker Has been your patient for 15 years Recently promoted as a corporate executive and is being asked to undergo a thorough medical evaluation including personal genome testing and would like to know your thoughts

Family history 26 Jim A&W 3 Judy A&W A&W N Prostate cancer d Hypertension Arthritis 54 Mid-50s A&W

What is direct-to-consumer genetic testing? Direct-to-consumer (DTC) genetic testing also referred to as personal genome testing – offered with the promise of providing: predictive genetic risk assessment for a variety of health conditions (i.e. diabetes, cancer, obesity) information about carrier status information regarding response to and/or side-effect risk of certain pharmaceuticals (i.e. clopidogrel, statins, antidepressants)

Uses odds ratios and relative risks to categorize an individual as at increased risk (higher than average), average, or at decreased risk (lower than average) Can also screen for single gene disorders (e.g. cystic fibrosis, HFE-associated hemochromatosis, BRCA) Can uncover medically irrelevant information such as bitter taste perception or curly hair What is direct-to-consumer genetic testing?

What do I need to know about the genetics of direct-to-consumer genetic testing? Uses data generated from genome-wide association studies (GWAS) – case-control studies which examine many common variations in our genetic code (single nucleotide polymorphisms [SNPs])* – compare large groups of individuals (unaffected controls versus individuals with symptoms of a specific disease) in an attempt to distinguish between non-harmful changes in the DNA code and pathogenic, disease-causing/predisposing changes SNPs (pronounced ‘snips’) are the most common type of genetic variation. Each SNP represents a difference in a single DNA building block, a nucleotide. SNPs occur normally in an individual’s genome about once in every 300 nucleotides, and so there are about 10 million SNPs in the human genome

Who can obtain direct-to-consumer genetic testing? Generally, direct-to-consumer (DTC) genetic testing is available online to anyone for a cost Genetic testing for DTC genetic testing is usually performed on a saliva sample

How will genetic testing help you and your patient? While there are limited data to support the clinical validity (ability to predict clinical outcome) and utility (the likelihood of improving patient outcome), some consumers might benefit from direct-to-consumer genetic testing as results may: – Encourage positive behaviour modifications (e.g. increase exercise, smoking cessation) – Provide useful information for medication choice and/or dose, or management – Provide information to individuals who have no or limited information about their family history (e.g. an individual who was adopted) – Reveal carrier status of a genetic condition that could have implications for family planning or medical management

Are there harms/limitations of direct-to- consumer genetic testing? Caution when interpreting direct-to-consumer (DTC) genetic testing should be exercised as: – DTC genetic testing does not take into account numerous factors important when interpreting genetic test results such as age, family history, lifestyle (e.g. smoking, obesity) and other environmental factors that are a significant contribution to common complex disease development – Questionable clinical utility of some of reported results – Family health history-based risk assessment is still the gold standard in the initial assessment for heritable conditions

No testing regulation Concerns re downstream testing and costs as result of direct-to-consumer (DTC) results “misattributed equivalence” – if a DTC test indicates a lower than average lifetime risk for a certain condition, when FH indicated a much higher risk, a consumer could be falsely reassured and not be as vigilant about medical interventions indicated by FH – This phenomenon speaks to the need for knowledgeable healthcare provider involvement in pre- and post-test counselling Are there harms/limitations of direct-to- consumer genetic testing?

Pearls – Direct-to-consumer (DTC) genetic testing is over-the- counter genetic testing available online to consumers through private companies – Generally, results report an individual’s probabilistic risk to develop a medical condition based on genome wide association studies (GWAS) – Results may provide medically useful information for consumers in addition to medically irrelevant information (e.g. curly hair) – Interpret DTC results with caution – Family health history-based risk assessment is still the gold standard in initial assessment for heritable conditions

References Aiyar et al. Risk estimates for complex disorders: comparing personal genome testing and family history. Genet Med 2013;. [Epub ahead of print] Goldsmith L et al. Direct-to-consumer genomic testing: systematic review of the literature on user perspectives. Eur J Hum Genet 2012; 20: Heald B et al. Prospective comparison of family medical history with personal genome screening for risk assessment of common cancers. Eur J Hum Genet 2012; 20(5): Special thanks to genetic counsellor Jill Davies at The Medcan Clinic