Noninvasive Prenatal Genetic Testing: Current and Emerging Ethical, Legal, and Social Issues

被引:67
|
作者
Minear, Mollie A. [1 ]
Alessi, Stephanie [2 ]
Allyse, Megan [3 ]
Michie, Marsha [4 ]
Chandrasekharan, Subhashini [5 ]
机构
[1] Duke Univ, Duke Sci & Soc, Durham, NC 27708 USA
[2] Stanford Univ, Stanford Ctr Biomed Eth, Stanford, CA 94305 USA
[3] Mayo Clin, Biomed Eth Program, Rochester, MN 55905 USA
[4] Univ Calif San Francisco, Inst Hlth & Aging, San Francisco, CA 94143 USA
[5] Duke Univ, Duke Global Hlth Inst, Durham, NC 27710 USA
关键词
informed decision making; genetic counseling; disability and reproductive rights; regulation and oversight; fetal genome sequencing; CELL-FREE DNA; FREE FETAL DNA; DOWN-SYNDROME; INFORMED-CONSENT; SEX SELECTION; DISABILITY RIGHTS; TERMINATION RATES; MATERNAL BLOOD; HIGH-RISK; DIAGNOSIS;
D O I
10.1146/annurev-genom-090314-050000
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Noninvasive prenatal genetic testing (NIPT) for chromosomal aneuploidy involving the analysis of cell-free fetal DNA became commercially available in 2011. The low false-positive rate of NIPT, which reduces unnecessary prenatal invasive diagnostic procedures, has led to broad clinician and patient adoption. We discuss the ethical, legal, and social issues raised by rapid and global dissemination of NIPT. The number of women using NIPT is anticipated to expand, and the number of conditions being tested for will continue to increase as well, raising concerns about the routinization of testing and negative impacts on informed decision making. Ensuring that accurate and balanced information is available to all pregnant women and that access to NIPT is equitable will require policy guidance from regulators, professional societies, and payers. Empirical evidence about stakeholders' perspectives and experiences will continue to be essential in guiding policy development so that advances in NIPT can be used effectively and appropriately to improve prenatal care.
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收藏
页码:369 / 398
页数:30
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