PRIORITIES FOR PUBLIC HEALTH GENOMICS
2012-2017
A Public Health Stakeholder Consultation
Co-Authors• Toby Citrin, JD
– [email protected]– Center for Public Health and Community
Genomics• Stephen M. Modell, MD, MS
– [email protected]– Center for Public Health and Community
Genomics• James O’Leary, BS
– Genetic Alliance
Presenter Disclosures
The following personal financial relationships with commercial interests relevant to this presentation existed during the past 12 months:
No Relationships to Disclose
Our Assignment from CDC/OPHGApril-December 2012
• Center for Public Health & Community Genomics– Consult stakeholders from public health
community (academe, practice and community) on the future of public health genomics in the next five years
– Collect, categorize, analyze input– Report findings at a wrap-up conference and in a
written report• Genetic Alliance
– Convene and organize the wrap-up conference
Planning Committee• Academe
– Karen Edwards– Sharon Kardia– Barbara Burns McGrath– Sara Shostak
• Practice– Sylvia Au– Suzanne Cupal– Deb Duquette– Karen Greendale
Planning Committee (Cont’d)
• Community– Winona Hollins-Hauge– Imogene Wiggs
• Ex Officio– Ella Greene-Moton (community liaison)– Dean Hosgood (APHA Genomics Forum)
Center Staff• Toby Citrin• Judy Daltuva• Nora Isack• Megan Knaus• Sally Meyer• Stephen Modell• Tevah Platt
RFI Responses• 62 responses• Site for review of responses:http://www.regulations.gov/#!docketDetail;dct=FR+PR+N+O+SR+PS;rpp=10;po=0;D=CDC-2011-0008• Spreadsheet and summaries in background
materials of written report
Interviews (9)• Practice
– Jean Chabut– Maxine Hayes– Stephen Teutsch– Deborah Klein Walker
• Academe– Wylie Burke– Kim Kaphingst– Chris Kuzawa– Ken Olden
• Community: Chickezie Maduka
Informal Discussions (3)
• National Community Committee – Special Interest Group on Genomics
• Public Health Practice• Genetic Alliance Annual Meeting –
“breakfast discussion”
Process Involved• Selection of Planning Committee• Themes identified from literature• RFI data organized into Word tables
and mapped on Nvivo• Planning Cmte. summary data review• Topics areas and sub-themes refined• Data organized into recommendations,
then refined after Bethesda meeting• Compilation of final report
Literature Review
• Workshops – Conferences – Reports - Program Reviews & Strategic Plans
• Articles on the Future of Public Health Genomics
• Articles on Stakeholder Consultation
Other Studies; Reports• Healthy People 2020• CDC/OPHG 10th Year Report (2008)• HRSA Strategic Plan• NHGRI Strategic Plan• IOM Roundtable on Translating Genomic-based
Research for Health• GAPPNet• Public Health Genomics Conference (2010)• SACGHS Education & Training Report (2011)• NHGRI Genomic Literacy Conference (11/2011)
Procedural Strengths• Preliminary work already done by CDC Office of
Public Health Genomics• Combination of federal RFI and University
expertise allowed for quick turn-around• Knowledgeable Planning Committee advised on
both general (e.g., frameworks) and specific (e.g., structuring of meetings) items
• Umbrella community and genetics advocacy organizations aided in recruitment and information gathering
Procedural Weaknesses
• Federal restriction to 9 key informant interviews
• Scope of the project limited the number of assessment avenues. Wiki had to be deferred.
• Short time window influenced information collation techniques used.
The ContextPast, Promise and Potential
• Progress in specific interventions, e.g.:– Newborn Screening– BRCA and Lynch Syndrome testing– Sudden cardiac death
• We’re a “half-way technology” needing translation, evidence and guidelines
• Near unanimous agreement by “insiders” on broader promise of public health genomics
• Lack of understanding or appreciation by “outsiders” of potential value of genomics to all of public health
What We Learned
Education
What We LearnedEducation -Health Literacy -
Professional Training
• Need for education of– the workforce (See SACGHS Report)– The public (“we’re still genomically illiterate”)– K-12– policy makers
What We Learned
Health Applications:Chronic Disease – Family Health History
• Increased emphasis on family history– Utilization by health depts. for risk
identification and early implementation of preventive measures
– Integration with EMRs – bridge between public health and medicine
– Need for validation, integration, marketing
Research
What We LearnedResearch: Translational – Impact on
Health Outcomes• Research base for decisions on screening• Cost-effectiveness of genetic technologies (e.g.,
family history)• “Research [providing] evidence that the segmentation
of populations by genomic characteristics would…achieve greater effectiveness and efficiency across a range of public health interventions, especially in the fields of obesity, diabetes, stroke, cancer and heart disease, and in neurodegenerative disorders.” – Ron Zimmern
What We LearnedResearch: Translational – Impact on
Health Outcomes (Continued)
• “…public health genomics demands that we understand—and address—how unequally distributed exposures, resources, and other factors outside the body enter into molecular processes to shape health and illness within and across populations.” – Sara Shostak
What We LearnedResearch – Infrastructure and Focus
• Integration of data sets/registries/tissue banks for research
• Database cataloguing genetics, physical and social environment, determinants of health
• Research focus toward public health goals and methods
• Role of CDC/OPHG – warehousing, guidance; “ushering” through the translation process
What We Learned
Assurance – Evidence Base
• Systems providing information on validity and utility of genetic tests– e.g., EGAPP but not as slow– OPHG role as trusted source of evidence
• “Leverage electronic healthcare infrastructure to achieve several goals: outcomes research, quality improvement, decision support.”– RFI Response
Policy Development
What We Learned
Policy Development
• Population level genetic screening• Utilization of family health history• FDA oversight of genetic tests• Advisory panel on multiplex screening• Regulation of direct-to-consumer testing
Funding
What We Learned
Funding• Support for state-level utilization of genomics
professionals• Support for integration of genomics
throughout public health practice• Funding of gene x environment research
bridging between medicine and public health• Funding CBPR utilizing genomic approaches• Funding to assure equal access to genetic
testing
Collaborations - Partnerships
What We Learned
Crosscutting:Collaborations - Partnerships
• Personalized medicine advisory board within OPHG
• NIH, AHRQ, CDC, CMS collaboration on evidence-based approaches
• State level: Chronic disease, labs, MCH and NBS collaboration
What We Learned
Crosscutting:Collaborations – Partnerships (Cont’d)• Schools of Public Health with State
Health Departments• Public-Private (e.g., with DTC
companies)• Transdisciplinary research teams
(genetics, social, behavioral)• Enhanced stakeholder engagement,
coordination and leadership
Role of CDC/OPHG in Furthering Collaborations and Partnerships
• Convener, e.g.,– with PRCs; chronic disease programs– Fostering interdisciplinary research
• Advocate– Liaison with APHA Genomics Forum
• Need for Advisory Group of stakeholders
Frameworks for Organization• Core Functions (IOM “Future” 1988)• From Genes to Public Health (Khoury, AJPH,
1996)• Core Functions & Essential Services
– Public Health in America – 1994– ASTHO - 2001)
• Ecological View (IOM “Future” 2002)– Strengthen all sectors of public health
Health DisparitiesCommunity Engagement
What We Learned
Health DisparitiesCommunity Engagement
• Gene x Environment – Epigenetic Research focused on health disparities
• Community-Based Participatory Research incorporating genomics (e.g. by PRC’s)
• “continue to seek out [the grassroots voice of the community], embracing the idea that community lies at the heart of public health….” – Ella Greene-Moton
Priorities Conference
• September 14, 2011• Over 70 leaders in public health
genomics– Academe, public health, health care,
community
Priorities ConferenceOverarching Objectives
• Improve public education about genetics through community engagement
• Continue working on issues related to evidence development
• Take a bottom-up approach to technology development
Priorities ConferenceOverarching Objectives
• Embed genetics into all aspects of healthcare
• Expand public health screening programs that utilize genetic information– Relates to cascade screening
recommendations in earlier presentation by Scott Bowen, et al
Summary1. PH Genomics has already achieved an impressive
track record in addressing less common diseases and has demonstrated its significant potential to advance all areas of public health
2. Currently available genetic tools still need to be embraced by public health (e.g., those described by Scott Bowen, et al, earlier in this session)
3. Realizing the future potential of PH genomics will require– Leadership and a common vision– Collaboration among currently separate groups– Infrastructure and education– Advocacy to secure resources and policies