Impact of Next Generation Sequencing on the Organization and Funding of Returning Research Results: Survey of Canadian Research Ethics Boards Members

被引:4
作者
Groisman, Iris Jaitovich [1 ]
Godard, Beatrice [1 ]
机构
[1] Univ Montreal, Inst Rech Sante Publ, Grp Rech Omics Eth, Montreal, PQ, Canada
来源
PLOS ONE | 2016年 / 11卷 / 05期
关键词
INCIDENTAL FINDINGS; GENETIC RESEARCH; GENOMIC RESEARCH; CHAIR PERSPECTIVES; INFORMED-CONSENT; PARTICIPANTS; CHALLENGES;
D O I
10.1371/journal.pone.0154965
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Research Ethics Boards (REBs) are expected to evaluate protocols planning the use of Next Generation Sequencing technologies (NGS), assuring that any genomic finding will be properly managed. As Canadian REBs play a central role in the disclosure of such results, we deemed it important to examine the views and experience of REB members on the return of aggregated research results, individual research results (IRRs) and incidental findings (IFs) in current genomic research. With this intent, we carried out a web-based survey, which showed that 59.7% of respondents viewed the change from traditional sequencing to NGS as more than a technical substitution, and that 77% of respondents agreed on the importance of returning aggregated research results, the most compelling reasons being the recognition of participants' contribution and increasing the awareness of scientific progress. As for IRRs specifically, 50% of respondents were in favour of conveying such information, even when they only indicated the probability that a condition may develop. Current regulations and risk to participants were considered equally important, and much more than financial costs, when considering the return of IRRs and IFs. Respondents indicated that the financial aspect of offering genetic counseling was the least important matter when assessing it as a requisite. Granting agencies were named as mainly responsible for funding, while the organizing and returning of IRRs and IFs belonged to researchers. However, views in these matters differ according to respondents' experience. Our results draw attention to the need for improved guidance when considering the organizational and financial aspects of returning genetic research results, so as to better fulfill the ethical and moral principles that are to guide such undertakings.
引用
收藏
页数:13
相关论文
共 28 条
  • [1] [Anonymous], 2014, TRIC POL STAT ETH CO
  • [2] Bad News about Bad News: The Disclosure of Risks to Insurability in Research Consent Processes
    Apold, Victoria Smith
    Downie, Jocelyn
    [J]. ACCOUNTABILITY IN RESEARCH-POLICIES AND QUALITY ASSURANCE, 2011, 18 (01): : 31 - 44
  • [3] Management and return of incidental genomic findings in clinical trials
    Ayuso, C.
    Millan, J. M.
    Dal-Re, R.
    [J]. PHARMACOGENOMICS JOURNAL, 2015, 15 (01) : 1 - 5
  • [4] Beskow Laura M, 2012, IRB, V34, P1
  • [5] Offering aggregate results to participants in genomic research: opportunities and challenges
    Beskow, Laura M.
    Burke, Wylie
    Fullerton, Stephanie M.
    Sharp, Richard R.
    [J]. GENETICS IN MEDICINE, 2012, 14 (04) : 490 - 496
  • [6] GENETIC-COUNSELING FOR FAMILIES WITH INHERITED SUSCEPTIBILITY TO BREAST AND OVARIAN-CANCER
    BIESECKER, BB
    BOEHNKE, M
    CALZONE, K
    MARKEL, DS
    GARBER, JE
    COLLINS, FS
    WEBER, BL
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1993, 269 (15): : 1970 - 1974
  • [7] Disclosure of individual genetic data to research participants: the debate reconsidered
    Bredenoord, Annelien L.
    Kroes, Hester Y.
    Cuppen, Edwin
    Parker, Michael
    van Delden, Johannes J. M.
    [J]. TRENDS IN GENETICS, 2011, 27 (02) : 41 - 47
  • [8] Return of results: Ethical and legal distinctions between research and clinical care
    Burke, Wylie
    Evans, Barbara J.
    Jarvik, Gail P.
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS, 2014, 166 (01) : 105 - 111
  • [9] CHAMBERLAIN JS, 1993, AM J HUM GENET, V52, P792
  • [10] Genomic Inheritances: Disclosing Individual Research Results From Whole-Exome Sequencing to Deceased Participants' Relatives
    Chan, Ben
    Facio, Flavia M.
    Eidem, Haley
    Hull, Sara Chandros
    Biesecker, Leslie G.
    Berkman, Benjamin E.
    [J]. AMERICAN JOURNAL OF BIOETHICS, 2012, 12 (10) : 1 - 8