ºÚÁÏÍø

Skip to main content

Funded by the National Institutes of Health, National Human Genome Research Institute R01HG012402

 

Team

Jean Cadigan, PhD, M-PI , MPP, JD, M-PI
University of North Carolina, School of Medicine University of Iowa, College of Law
, PhD, Co-investigator , JD, Co-investigator
Mayo Clinic, Department of Biomedical Ethics
George Washington University, School of Medicine and Health Sciences
Ìý Ìý
, PhD Courtney Canter, MA
University of North Carolina, School of Medicine University of North Carolina, School of Medicine
Ìý Ìý
Kriste Kuczynski, BA (Project Manager) Sara Watson, MA
University of North Carolina, School of Medicine Mayo Clinic, Department of Biomedical Ethics
Ìý Ìý
Lia Kaz, MSW , MA, MPH
University of North Carolina, School of Medicine University of Iowa, Department of Geographical and Sustainability Sciences
Ìý Ìý
Preya Agam, MPH
Ìý, MA
Mayo Clinic, Department of Biomedical Ethics University of North Carolina, School of Medicine

 

 

Project Description

In traditional predictive genetic testing, like for BRCA or Huntington’s Disease, single gene variants are analyzed to determine whether an individual is at high risk of developing a disease. The vast majority of diseases, however, are polygenic— caused by many different genes. Polygenic scores (PGS) have been heralded for their promise to predict risk for these more complex diseases like heart disease or diabetes by measuring the contribution of hundreds or thousands of genetic variants at once. Yet beyond prediction of health outcomes, the realm of ‘sociogenomics’ is developing scores measuring genetic contributions to social and behavioral factors, such as risk tolerance, income, educational attainment, sexuality, or optimism. Sociogenomic PGS often blur the lines between medical and social outcomes, such as with scores for drinking, smoking, or reproductive behavior.Ìý

This project addresses the following research questions:

  • What are the current trends and potential future development of sociogenomic PGS and what are the possible uses of scores in social settings?
  • How do various stakeholders perceive the benefits and risks of sociogenomic PGS?
  • How well do existing laws and policies protect against the potential harms of sociogenomic PGS and promote the benefits?

Specific Aims

  1. Using horizon scanning methodologies, map the landscape of sociogenomic PGS, their potential uses, and how sociogenomic research findings are presented to and consumed by the public.
  2. Enlist those involved in the pipeline of sociogenomics research (biobank participants, PGS researchers, and social scientists) to examine and assess their attitudes toward the range of harms and benefits of sociogenomic PGS, the blurring of the line between social and medical traits, and the implications of varying uses of PGS in social settings.
  3. Conduct a legal and policy analysis of how current legal rules protect against potential misuse and/or promote possible benefits of sociogenomic findings.

The product of this project will be a set of case studies designed to help policy makers, the research community and the public anticipate and mitigate the potential harms of employing sociogenomic PGS in various social settings, while identifying and maximizing potential benefits.ÌýÌý

 

Advisory Board

, MS, CGC, Howard University College of Medicine, Washington, DC

Gail Henderson, PhD, University of North Carolina School of Medicine, Chapel Hill, NC

, PhD, Mount Sinai University, Icahn School of Medicine, New York City, NY

PhD, University of Chicago, Chicago, IL

, PhD, The Hastings Center, Garrison, NY

, PhD, Broad Institute of MIT and Harvard University, Cambridge, MA

 

Publications