Rethinking the "open future" argument against predictive genetic testing of children

被引:50
作者
Garrett, Jeremy R. [1 ,2 ]
Lantos, John D. [1 ,2 ]
Biesecker, Leslie G. [3 ]
Childerhose, Janet E. [4 ]
Chung, Wendy K. [5 ,6 ]
Holm, Ingrid A. [7 ,8 ,9 ]
Koenig, Barbara A. [10 ]
McEwen, Jean E. [3 ]
Wilfond, Benjamin S. [11 ,12 ]
Brothers, Kyle [13 ]
Berkman, Benjamin [14 ]
Bernhardt, Barbara [15 ]
Caga-Anan, Charlisse [16 ]
Clayton, Ellen Wright [17 ]
Goldenberg, Aaron [18 ]
Hull, Sara Chandros [14 ]
Joffe, Steve [15 ]
Krantz, Ian [19 ]
Lewis, Michelle [20 ]
Liang, Wayne [21 ]
Lockhart, Nicole [22 ]
McCollum, Susana [23 ]
McCullough, Larry [23 ]
McGuire, Amy [23 ]
Noorbaksh, Ali [23 ]
Panchang, Sarita [23 ]
Parsons, D. Will [23 ]
Reiss, Jacob [24 ]
Roche, Myra [25 ]
Rodriguez, Laura [22 ]
Romasko, Edward [19 ]
Ross, Lainie Friedman [26 ]
Sharp, Richard [27 ]
Skinner, Debra [25 ]
Slashinski, Melody [28 ]
Tabor, Holly [29 ]
Tomlinson, Ashley [15 ]
Wolf, Susan [30 ]
Yu, Joon-Ho [31 ]
机构
[1] Childrens Mercy Kansas City, Childrens Mercy Bioeth Ctr, Kansas City, MO USA
[2] Univ Missouri, Dept Pediat, Kansas City, MO 64110 USA
[3] NHGRI, NIH, Bethesda, MD 20892 USA
[4] Univ Louisville, Sch Med, Divis Pediat Clin & Translat Res, Louisville, KY 40292 USA
[5] Columbia Univ, Dept Med, New York, NY USA
[6] Columbia Univ, Dept Pediat, New York, NY 10027 USA
[7] Boston Childrens Hosp, Harvard Med Sch, Div Genet & Genom, Boston, MA USA
[8] Boston Childrens Hosp, Harvard Med Sch, Manton Ctr Orphan Dis Res, Boston, MA USA
[9] Boston Childrens Hosp, Harvard Med Sch, Dept Pediat, Boston, MA USA
[10] Univ Calif San Francisco, UCSF Bioeth, San Francisco, CA 94143 USA
[11] Seattle Childrens Res Inst, Treuman Katz Bioeth Ctr, Seattle, WA USA
[12] Univ Washington, Dept Pediat, Seattle, WA 98195 USA
[13] Univ Louisville, Dept Pediat, Louisville, KY 40292 USA
[14] NIH, Dept Bioeth, Bldg 10, Bethesda, MD 20892 USA
[15] Univ Penn, Philadelphia, PA 19104 USA
[16] NCI, Bethesda, MD 20892 USA
[17] Vanderbilt Univ, Med Ctr, 221 Kirkland Hall, Nashville, TN 37235 USA
[18] Case Western Reserve Univ, Cleveland, OH 44106 USA
[19] Childrens Hosp Philadelphia, Philadelphia, PA USA
[20] John Hopkins Berman Inst Bioeth, Baltimore, MD USA
[21] Univ Alabama Birmingham, Birmingham, AL USA
[22] NGHRI, Bethesda, MD USA
[23] Baylor Coll Med, Houston, TX 77030 USA
[24] Kaiser Permanente Northwest, Washington, DC USA
[25] Univ N Carolina, Chapel Hill, NC 27515 USA
[26] Univ Chicago, Chicago, IL 60637 USA
[27] Mayo Clin, Rochester, MN USA
[28] Univ Massachusetts Amherst, Amherst, MA USA
[29] Stanford Univ, Stanford, CA 94305 USA
[30] Univ Minnesota, Minneapolis, MN 55455 USA
[31] Univ Washington, Seattle, WA 98195 USA
关键词
adult-onset conditions; children's interests; pediatric genetic testing; right to an open future; secondary findings; ADULT-ONSET CONDITIONS; HUNTINGTON DISEASE; DECISION-MAKING; ATHLETIC TALENT; ETHICAL-ISSUES; YOUNG-PEOPLE; MINORS; INFORMATION; INTERESTS; ENHANCEMENT;
D O I
10.1038/s41436-019-0483-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Professional consensus has traditionally discouraged predictive genetic testing when no childhood interventions can reduce future morbidity or mortality. However, advances in genome sequencing and accumulating evidence that children and families cope adequately with predictive genetic information have weakened this consensus. The primary argument remaining against testing appeals to children's "right to an open future." It claims that the autonomy of the future adult is violated when others make an irreversible choice to obtain or disclose predictive genetic information during childhood. We evaluate this argument and conclude that children's interest in an open future should not be understood as a right. Rather an open future is one significant interest to weigh against other important interests when evaluating decisions. Thus, predictive genetic testing is ethically permissible in principle, as long as the interests promoted outweigh potential harms. We conclude by offering an expanded model of children's interests that might be considered in such circumstances, and present two case analyses to illustrate how this framework better guides decisions about predictive genetic testing in pediatrics.
引用
收藏
页码:2190 / 2198
页数:9
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