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Use of next generation sequencing technologies in research and beyond: are participants with mental health disorders fully protected?
BACKGROUND: Next Generation Sequencing (NGS) is expected to help find the elusive, causative genetic defects associated with Bipolar Disorder (BD). This article identifies the importance of NGS and further analyses the social and ethical implications of this approach when used in research projects s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3537639/ https://www.ncbi.nlm.nih.gov/pubmed/23256847 http://dx.doi.org/10.1186/1472-6939-13-36 |
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author | Groisman, Iris Jaitovich Mathieu, Ghislaine Godard, Beatrice |
author_facet | Groisman, Iris Jaitovich Mathieu, Ghislaine Godard, Beatrice |
author_sort | Groisman, Iris Jaitovich |
collection | PubMed |
description | BACKGROUND: Next Generation Sequencing (NGS) is expected to help find the elusive, causative genetic defects associated with Bipolar Disorder (BD). This article identifies the importance of NGS and further analyses the social and ethical implications of this approach when used in research projects studying BD, as well as other psychiatric ailments, with a view to ensuring the protection of research participants. METHODS: We performed a systematic review of studies through PubMed, followed by a manual search through the titles and abstracts of original articles, including the reviews, commentaries and letters published in the last five years and dealing with the ethical and social issues raised by NGS technologies and genomics studies of mental disorders, especially BD. A total of 217 studies contributed to identify the themes discussed herein. RESULTS: The amount of information generated by NGS renders individuals suffering from BD particularly vulnerable, and increases the need for educational support throughout the consent process, and, subsequently, of genetic counselling, when communicating individual research results and incidental findings to them. Our results highlight the importance and difficulty of respecting participants’ autonomy while avoiding any therapeutic misconception. We also analysed the need for specific regulations on the use and communication of incidental findings, as well as the increasing influence of NGS in health care. CONCLUSIONS: Shared efforts on the part of researchers and their institutions, Research Ethics Boards as well as participants’ representatives are needed to delineate a tailored consent process so as to better protect research participants. However, health care professionals involved in BD care and treatment need to first determine the scientific validity and clinical utility of NGS-generated findings, and thereafter their prevention and treatment significance. |
format | Online Article Text |
id | pubmed-3537639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35376392013-01-10 Use of next generation sequencing technologies in research and beyond: are participants with mental health disorders fully protected? Groisman, Iris Jaitovich Mathieu, Ghislaine Godard, Beatrice BMC Med Ethics Research Article BACKGROUND: Next Generation Sequencing (NGS) is expected to help find the elusive, causative genetic defects associated with Bipolar Disorder (BD). This article identifies the importance of NGS and further analyses the social and ethical implications of this approach when used in research projects studying BD, as well as other psychiatric ailments, with a view to ensuring the protection of research participants. METHODS: We performed a systematic review of studies through PubMed, followed by a manual search through the titles and abstracts of original articles, including the reviews, commentaries and letters published in the last five years and dealing with the ethical and social issues raised by NGS technologies and genomics studies of mental disorders, especially BD. A total of 217 studies contributed to identify the themes discussed herein. RESULTS: The amount of information generated by NGS renders individuals suffering from BD particularly vulnerable, and increases the need for educational support throughout the consent process, and, subsequently, of genetic counselling, when communicating individual research results and incidental findings to them. Our results highlight the importance and difficulty of respecting participants’ autonomy while avoiding any therapeutic misconception. We also analysed the need for specific regulations on the use and communication of incidental findings, as well as the increasing influence of NGS in health care. CONCLUSIONS: Shared efforts on the part of researchers and their institutions, Research Ethics Boards as well as participants’ representatives are needed to delineate a tailored consent process so as to better protect research participants. However, health care professionals involved in BD care and treatment need to first determine the scientific validity and clinical utility of NGS-generated findings, and thereafter their prevention and treatment significance. BioMed Central 2012-12-20 /pmc/articles/PMC3537639/ /pubmed/23256847 http://dx.doi.org/10.1186/1472-6939-13-36 Text en Copyright ©2012 Groisman et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Groisman, Iris Jaitovich Mathieu, Ghislaine Godard, Beatrice Use of next generation sequencing technologies in research and beyond: are participants with mental health disorders fully protected? |
title | Use of next generation sequencing technologies in research and beyond: are participants with mental health disorders fully protected? |
title_full | Use of next generation sequencing technologies in research and beyond: are participants with mental health disorders fully protected? |
title_fullStr | Use of next generation sequencing technologies in research and beyond: are participants with mental health disorders fully protected? |
title_full_unstemmed | Use of next generation sequencing technologies in research and beyond: are participants with mental health disorders fully protected? |
title_short | Use of next generation sequencing technologies in research and beyond: are participants with mental health disorders fully protected? |
title_sort | use of next generation sequencing technologies in research and beyond: are participants with mental health disorders fully protected? |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3537639/ https://www.ncbi.nlm.nih.gov/pubmed/23256847 http://dx.doi.org/10.1186/1472-6939-13-36 |
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