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Privacy protection and public goods: building a genetic database for health research in Newfoundland and Labrador

OBJECTIVE: To provide a legal and ethical analysis of some of the implementation challenges faced by the Population Therapeutics Research Group (PTRG) at Memorial University (Canada), in using genealogical information offered by individuals for its genetics research database. MATERIALS AND METHODS:...

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Autores principales: Kosseim, Patricia, Pullman, Daryl, Perrot-Daley, Astrid, Hodgkinson, Kathy, Street, Catherine, Rahman, Proton
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3555321/
https://www.ncbi.nlm.nih.gov/pubmed/22859644
http://dx.doi.org/10.1136/amiajnl-2012-001009
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author Kosseim, Patricia
Pullman, Daryl
Perrot-Daley, Astrid
Hodgkinson, Kathy
Street, Catherine
Rahman, Proton
author_facet Kosseim, Patricia
Pullman, Daryl
Perrot-Daley, Astrid
Hodgkinson, Kathy
Street, Catherine
Rahman, Proton
author_sort Kosseim, Patricia
collection PubMed
description OBJECTIVE: To provide a legal and ethical analysis of some of the implementation challenges faced by the Population Therapeutics Research Group (PTRG) at Memorial University (Canada), in using genealogical information offered by individuals for its genetics research database. MATERIALS AND METHODS: This paper describes the unique historical and genetic characteristics of the Newfoundland and Labrador founder population, which gave rise to the opportunity for PTRG to build the Newfoundland Genealogy Database containing digitized records of all pre-confederation (1949) census records of the Newfoundland founder population. In addition to building the database, PTRG has developed the Heritability Analytics Infrastructure, a data management structure that stores genotype, phenotype, and pedigree information in a single database, and custom linkage software (KINNECT) to perform pedigree linkages on the genealogy database. DISCUSSION: A newly adopted legal regimen in Newfoundland and Labrador is discussed. It incorporates health privacy legislation with a unique research ethics statute governing the composition and activities of research ethics boards and, for the first time in Canada, elevating the status of national research ethics guidelines into law. The discussion looks at this integration of legal and ethical principles which provides a flexible and seamless framework for balancing the privacy rights and welfare interests of individuals, families, and larger societies in the creation and use of research data infrastructures as public goods. CONCLUSION: The complementary legal and ethical frameworks that now coexist in Newfoundland and Labrador provide the legislative authority, ethical legitimacy, and practical flexibility needed to find a workable balance between privacy interests and public goods. Such an approach may also be instructive for other jurisdictions as they seek to construct and use biobanks and related research platforms for genetic research.
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spelling pubmed-35553212013-12-14 Privacy protection and public goods: building a genetic database for health research in Newfoundland and Labrador Kosseim, Patricia Pullman, Daryl Perrot-Daley, Astrid Hodgkinson, Kathy Street, Catherine Rahman, Proton J Am Med Inform Assoc Focus on Patient Privacy OBJECTIVE: To provide a legal and ethical analysis of some of the implementation challenges faced by the Population Therapeutics Research Group (PTRG) at Memorial University (Canada), in using genealogical information offered by individuals for its genetics research database. MATERIALS AND METHODS: This paper describes the unique historical and genetic characteristics of the Newfoundland and Labrador founder population, which gave rise to the opportunity for PTRG to build the Newfoundland Genealogy Database containing digitized records of all pre-confederation (1949) census records of the Newfoundland founder population. In addition to building the database, PTRG has developed the Heritability Analytics Infrastructure, a data management structure that stores genotype, phenotype, and pedigree information in a single database, and custom linkage software (KINNECT) to perform pedigree linkages on the genealogy database. DISCUSSION: A newly adopted legal regimen in Newfoundland and Labrador is discussed. It incorporates health privacy legislation with a unique research ethics statute governing the composition and activities of research ethics boards and, for the first time in Canada, elevating the status of national research ethics guidelines into law. The discussion looks at this integration of legal and ethical principles which provides a flexible and seamless framework for balancing the privacy rights and welfare interests of individuals, families, and larger societies in the creation and use of research data infrastructures as public goods. CONCLUSION: The complementary legal and ethical frameworks that now coexist in Newfoundland and Labrador provide the legislative authority, ethical legitimacy, and practical flexibility needed to find a workable balance between privacy interests and public goods. Such an approach may also be instructive for other jurisdictions as they seek to construct and use biobanks and related research platforms for genetic research. BMJ Group 2013 /pmc/articles/PMC3555321/ /pubmed/22859644 http://dx.doi.org/10.1136/amiajnl-2012-001009 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/3.0/ and http://creativecommons.org/licenses/by-nc/3.0/legalcode
spellingShingle Focus on Patient Privacy
Kosseim, Patricia
Pullman, Daryl
Perrot-Daley, Astrid
Hodgkinson, Kathy
Street, Catherine
Rahman, Proton
Privacy protection and public goods: building a genetic database for health research in Newfoundland and Labrador
title Privacy protection and public goods: building a genetic database for health research in Newfoundland and Labrador
title_full Privacy protection and public goods: building a genetic database for health research in Newfoundland and Labrador
title_fullStr Privacy protection and public goods: building a genetic database for health research in Newfoundland and Labrador
title_full_unstemmed Privacy protection and public goods: building a genetic database for health research in Newfoundland and Labrador
title_short Privacy protection and public goods: building a genetic database for health research in Newfoundland and Labrador
title_sort privacy protection and public goods: building a genetic database for health research in newfoundland and labrador
topic Focus on Patient Privacy
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3555321/
https://www.ncbi.nlm.nih.gov/pubmed/22859644
http://dx.doi.org/10.1136/amiajnl-2012-001009
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