Genomic Research and American Indian Tribal Communities in Oklahoma: Learning From Past Research Misconduct and Building Future Trusting Partnerships

Author:

Chadwick Jennifer Q1,Copeland Kenneth C1,Branam Dannielle E2,Erb-Alvarez Julie A3,Khan Sohail I4,Peercy Michael T5,Rogers Mark E6,Saunkeah Bobby R5,Tryggestad Jeanie B1,Wharton David F2

Affiliation:

1. Department of Pediatrics, Section of Diabetes and Endocrinology, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma

2. Heath Services Authority, Choctaw Nation of Oklahoma, Durant, Oklahoma

3. Oklahoma City Area Indian Health Service, Oklahoma City, Oklahoma

4. Department of Health Research, Cherokee Nation, Tahlequah, Oklahoma

5. Department of Health, Division of Research and Public Health, The Chickasaw Nation, Ada, Oklahoma

6. Tribal Health System, Absentee Shawnee Tribe, Shawnee, Oklahoma

Abstract

Abstract Research misconduct and consequential harms have been inflicted upon American Indian/Alaska Native communities for decades. To protect their people and culture and to retain oversight over research, many Native communities have established tribal health research and institutional review boards. The Treatment Options for Type 2 Diabetes in Adolescents and Youth (TODAY) Study showcases a successful, trusting research collaboration with tribal nations and academic investigators in Oklahoma. In 2006, the TODAY Study investigators proposed a modification of the study protocol to collect biological specimens from participants for genomic analyses and indefinite storage. Partnering American Indian tribal nations elected not to participate in the genomics collection and repository proposal. Reasons included 1) protection of cultural values, 2) concerns regarding community anonymity, 3) a potential threat to tribal services eligibility, 4) broad informed consent language, and 5) vague definitions of data access and usage. The nations believed the proposed genomics analyses presented a risk of harm to their people and nations without clear benefit. Since the 2006 proposal and the advancement of genomics research, many tribal communities in Oklahoma, appreciating the potential benefits of genomic research, are developing policies regarding oversight of/access to data and biological specimens to mitigate risks and provide members and communities with opportunities to participate in safe and meaningful genomic research.

Funder

National Institute of Diabetes and Digestive and Kidney Diseases

Office of the Director

National Institutes of Health

National Center for Research Resources

Washington University School of Medicine

Children’s Hospital Los Angeles

University of Colorado Denver

Children’s Hospital of Pittsburgh

Massachusetts General Hospital

Yale University

University of Oklahoma Health Sciences Center

Children’s Hospital of Philadelphia

Case Western Reserve University

Washington University in St. Louis

Publisher

Oxford University Press (OUP)

Subject

Epidemiology

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