A proposal on the first Japanese practical guidance for the return of individual genomic results in research settings.
Journal
Journal of human genetics
ISSN: 1435-232X
Titre abrégé: J Hum Genet
Pays: England
ID NLM: 9808008
Informations de publication
Date de publication:
Mar 2020
Mar 2020
Historique:
received:
25
06
2019
accepted:
19
11
2019
revised:
19
11
2019
pubmed:
25
12
2019
medline:
10
10
2020
entrez:
25
12
2019
Statut:
ppublish
Résumé
Large-scale, low-cost genome analysis has become possible with next-generation sequencing technology, which is currently used in research and clinical practice. Many attempts of returning individual genomic results have commenced not only in clinical practice, but also in research settings of several countries. In Japan, the government guidelines include a section on the disclosure of genetic information regarding genome analysis in research. However, no practical guidance for the return of individual genomic results in research settings (ROGRR) currently exists. We propose practical guidance regarding ROGRR in Japan based on extensive research, including a literature review of related previous studies, an examination of the relevant legislation in Japan, and interviews with stakeholders. The guidance we developed consists of "Points to consider" and "Issues for further discussion and consideration." The "Points to consider" were divided into five parts, from preliminary review before discussion of policy, to the actual return and follow-up process, in the order of the assumed ROGRR process. It is anticipated that a situation will arise where numerous research projects will consider ROGRR carefully and realistically in the future, and in the process of drafting such practical guidance, various issues requiring continuous discussion will emerge. The necessities of continuous discussion concerning ROGRR in Japan's context is increasing, particularly in terms of the ethical, legal, and social implications. We believe such discussions and considerations may contribute to creating a new system that will increase availability of personalized medicine and prevention using genetic information, allowing them to become useful to the broader population.
Identifiants
pubmed: 31873219
doi: 10.1038/s10038-019-0697-y
pii: 10.1038/s10038-019-0697-y
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
251-261Subventions
Organisme : Japan Agency for Medical Research and Development (AMED)
ID : 18km0405301
Organisme : Japan Agency for Medical Research and Development (AMED)
ID : 18km0405301
Organisme : Japan Agency for Medical Research and Development (AMED)
ID : 18km0405301
Organisme : Japan Agency for Medical Research and Development (AMED)
ID : 18km0405301
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