To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts

被引:122
作者
Christenhusz, Gabrielle M. [1 ]
Devriendt, Koenraad [2 ]
Dierickx, Kris [1 ]
机构
[1] Catholic Univ Louvain, Ctr Biomed Eth & Law, B-3000 Louvain, Belgium
[2] Catholic Univ Louvain, Ctr Human Genet, B-3000 Louvain, Belgium
关键词
incidental findings; ethics; research; clinical genetics; whole genome sequencing; RESEARCH PARTICIPANTS; GENOMIC RESEARCH; CHALLENGE; TESTS; PROGRAMS; SCIENCE;
D O I
10.1038/ejhg.2012.130
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Any test that produces visual images or digital or genetic sequences will tend to produce incidental findings because more will be visible than what was originally sought. We conducted a systematic review of the ethical reasons presented in the literature for and against the disclosure of incidental findings arising in clinical and research genetics contexts A search of electronic databases resulted in 13 articles included for systematic review. Articles presented reasons for and against disclosure, and reasons for proceeding with caution when making decisions about disclosure. One major recommendation of the reviewed articles is in favor of qualified disclosure: incidental findings with confirmed clinical utility where there is the possibility of treatment or prevention should be disclosed, with exceptions. A second type of recommendation is that disclosure should proceed with caution, especially in the context of new genetic technologies and genetic testing involving minors. It is also recommended that the number of possible incidental findings be limited even before genetic testing is carried out. Such a policy, which we advocate, would show preference for non-disclosure. European Journal of Human Genetics (2013) 21, 248-255; doi:10.1038/ejhg.2012.130; published online 27 June 2012
引用
收藏
页码:248 / 255
页数:8
相关论文
共 38 条
[1]   Whole Genome Scanning: Resolving Clinical Diagnosis and Management Amidst Complex Data [J].
Ali-Khan, Sarah E. ;
Daar, Abdallah S. ;
Shuman, Cheryl ;
Ray, Peter N. ;
Scherer, Stephen W. .
PEDIATRIC RESEARCH, 2009, 66 (04) :357-363
[2]   Exome sequencing as a tool for Mendelian disease gene discovery [J].
Bamshad, Michael J. ;
Ng, Sarah B. ;
Bigham, Abigail W. ;
Tabor, Holly K. ;
Emond, Mary J. ;
Nickerson, Deborah A. ;
Shendure, Jay .
NATURE REVIEWS GENETICS, 2011, 12 (11) :745-755
[3]  
BOTKIN JR, 1995, J CLIN ETHIC, V6, P182
[4]   Categorizing genetic tests to identify their ethical, legal, and social implications [J].
Burke, W ;
Pinsky, LE ;
Press, NA .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 106 (03) :233-240
[5]   Genetic Screening [J].
Burke, Wylie ;
Tarini, Beth ;
Press, Nancy A. ;
Evans, James P. .
EPIDEMIOLOGIC REVIEWS, 2011, 33 (01) :148-164
[6]   Research ethics recommendations for whole-genome research: Consensus statement [J].
Caulfield, Timothy ;
McGuire, Amy L. ;
Cho, Mildred ;
Buchanan, Janet A. ;
Burgess, Michael M. ;
Danilczyk, Ursula ;
Diaz, Christina M. ;
Fryer-Edwards, Kelly ;
Green, Shane K. ;
Hodosh, Marc A. ;
Juengst, Eric T. ;
Kaye, Jane ;
Kedes, Laurence ;
Knoppers, Bartha Maria ;
Lemmens, Trudo ;
Meslin, Eric M. ;
Murphy, Juli ;
Nussbaum, Robert L. ;
Otlowski, Margaret ;
Pullman, Daryl ;
Ray, Peter N. ;
Sugarman, Jeremy ;
Timmons, Michael .
PLOS BIOLOGY, 2008, 6 (03) :430-435
[7]   Understanding incidental findings in the context of genetics and genomics [J].
Cho, Mildred K. .
JOURNAL OF LAW MEDICINE & ETHICS, 2008, 36 (02) :280-+
[8]   Incidental findings in genetics research using archived DNA [J].
Clayton, Ellen Wright .
JOURNAL OF LAW MEDICINE & ETHICS, 2008, 36 (02) :286-+
[9]   Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data [J].
Cooper, Gregory M. ;
Shendure, Jay .
NATURE REVIEWS GENETICS, 2011, 12 (09) :628-640
[10]   Looking ahead, looking behind INTRODUCTION [J].
Evans, James P. .
GENETICS IN MEDICINE, 2011, 13 (03) :177-178