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

Annual Review of Genomics and Human Genetics - Tập 16 Số 1 - Trang 369-398 - 2015
Mollie Minear1, Stephanie A. Alessi2, Megan Allyse3, Marsha Michie4, Subhashini Chandrasekharan5
1Duke Science & Society, Duke University, Durham, North Carolina 27708.
2Stanford Center for Biomedical Ethics, Stanford University, Stanford, California 94305
3Biomedical Ethics Program, Mayo Clinic, Rochester, Minnesota 55905
4Institute for Health and Aging, University of California, San Francisco, California 94143
5Duke Global Health Institute, Duke University, Durham, North Carolina 27710;

Tóm tắt

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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Tài liệu tham khảo

10.1136/bmj.322.7284.463

10.1002/pd.4101

10.1136/bmj.38922.516204.55

10.1177/096973300100800408

5. Allyse M, Chandrasekharan S. 2015. Too much, too soon? Commercial provision of noninvasive prenatal screening for subchromosomal abnormalities and beyond.Genet. Med.In press. doi: 10.1038/gim.2015.23

10.1080/23294515.2014.994722

10.1002/pd.4144

10.1093/humrep/des286

10.1097/01.AOG.0000423819.85283.f4

10.1097/00006250-200701000-00054

11. Ariosa Diagn. 2015.FAQs for healthcare providers.http://www.ariosadx.com/healthcare-professionals/faqs

12. Asch A. 2000. Why I haven't changed my mind about prenatal diagnosis: reflections and refinements. See Ref. 148, pp. 234–58

Asch A, 2002, Fla. State Univ. Law Rev., 30, 315

10.1017/CBO9780511614590.008

10.1016/j.ajog.2012.01.029

10.1002/uog.12299

10.1097/AOG.0000000000000145

Barot S, 2012, Guttmacher Policy Rev., 15, 18

10.1038/gim.2014.20

10.1016/j.ajog.2014.01.014

10.1002/pd.4139

10.1002/pd.4272

10.1002/pd.4366

10.1002/1097-0223(200101)21:1<46::AID-PD984>3.0.CO;2-C

10.1007/s10897-013-9605-3

10.1038/gim.2012.113

27. BGI. 2014. BGI is granted patent in 16 countries for non-invasive prenatal genetic test technology.BGI News, Oct. 10.http://www.genomics.cn/en/news/show_news?nid=104192

28. BGI. 2014.FAQs.http://www.niftytest.com/healthcare-providers/faqs

29. BGI. 2014.Introduction to NIFTY™.http://www.niftytest.com/healthcare-providers/intro-to-nifty

10.1002/pd.4229

10.1056/NEJMoa1311037

10.1097/AOG.0000000000000637

10.1373/clinchem.2013.202663

10.1007/BF02547888

10.1016/j.socscimed.2014.02.025

10.1363/3411008

10.1080/02646830500129214

10.1002/pd.4382

39. Cent. Medicare Medicaid Serv. 2015.Pregnant women.http://www.medicaid.gov/medicaid-chip-program-information/by-population/pregnant-women/pregnant-women.html

10.1002/pd.4445

10.1126/scitranslmed.3008704

42. Chen SJ. 2014. China cracks down on DNA testing.Forbes, Mar. 3.http://www.forbes.com/sites/shuchingjeanchen/2014/03/03/china-cracks-down-on-dna-testing-2

10.1002/pd.4125

10.1002/pd.4024

10.1038/ejhg.2012.217

10.1002/pd.4157

10.1002/pd.1913

10.1080/00220380412331293807

10.1038/ejhg.2009.203

10.1007/s10728-010-0146-8

10.1136/medethics-2011-100180

10.1001/jama.2011.1114

10.1016/j.ijgo.2013.11.001

Dixon DP, 2008, Issues Law Med., 24, 3

55. Dondorp W, de Wert G, Bombard Y, Bianchi DW, Bergmann C, et al. 2015. Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.Eur. J. Hum. Genet.In press. doi: 10.1038/ejhg.2015.57

10.1002/hast.50

10.1016/j.ajog.2008.12.027

10.1111/j.1460-9592.2005.01597.x

Edwins J, 2000, Pract. Midwife, 3, 21

10.1002/uog.14693

Faden RR, 1986, A History and Theory of Informed Consent

10.2105/AJPH.75.12.1381

10.3390/jcm3020614

10.1007/s10897-012-9484-z

10.1159/000116738

66. FDA (Food Drug Admin.). 2014.Draft guidance for industry, Food and Drug Administration staff, and clinical laboratories: framework for regulatory oversight of laboratory developed tests(LDTs). Guid. Doc. 1739, FDA, Silver Spring, MD.http://www.fda.gov/downloads/MedicalDevices/DeviceRegulationandGuidance/GuidanceDocuments/UCM416685.pdf

10.2105/AJPH.2012.301197

68. Finlay JE, Canning D, Po JY. 2012.Reproductive health laws around the world. Work. Pap. 96, Program Glob. Demogr. Aging, Harvard Univ.http://www.hsph.harvard.edu/program-on-the-global-demography-of-aging/WorkingPapers/2012/PGDA_WP_96.pdf

10.1017/S1744552313000074

70. French HW. 2005. As girls “vanish,” Chinese city battles tide of abortions.New York Times, Feb. 17.http://www.nytimes.com/2005/02/17/international/asia/17china.html

71. GenomeWeb Staff Report. 2013. Shareholder sues Sequenom, alleging illegal “capping” of MaterniT21 Plus price to induce test adoption.GenomeWeb, Oct. 3.https://www.genomeweb.com/sequencing/shareholder-sues-sequenom-alleging-illegal-capping-maternit21-plus-price-induce

72. GenomeWeb Staff Report. 2014. BGI suspends clinical NGS-based trisomy testing in China.GenomeWeb, Mar. 14.https://www.genomeweb.com/sequencing/bgi-suspends-clinical-ngs-based-trisomy-testing-china

73. GenomeWeb Staff Report. 2014. China FDA approves BGI's NGS products.GenomeWeb, July 2.https://www.genomeweb.com/sequencing/china-fda-approves-bgis-ngs-products

74. GenomeWeb Staff Report. 2014. Illumina, Sequenom pool NIPT patents, settling IP disputes.GenomeWeb, Dec. 3.https://www.genomeweb.com/business-news/illumina-sequenom-pool-nipt-patents-settling-ip-disputes

75. GenomeWeb Staff Report. 2015. Berry Genomics lands China FDA approval for NIPT sequencer.GenomeWeb, Mar. 31.https://www.genomeweb.com/regulatory-news/berry-genomics-lands-china-fda-approval-nipt-sequencer

76. GenomeWeb Staff Report. 2015. Illumina sues Premaitha Health over NIPT IP; Swiss firm adopts Premaitha's Iona CE-IVD test.GenomeWeb, Mar. 16.https://www.genomeweb.com/business-news/illumina-sues-premaitha-health-over-nipt-ip-swiss-firm-adopts-premaithas-iona-ce-ivd

10.1002/uog.14791

10.1038/nbt.2568

79. Green JM, Hewison J, Bekker HL, Bryant LD, Cuckle HS. 2004.Psychosocial aspects of genetic screening of pregnant women and newborns: a systematic review. Health Technol. Assess. 8(33), Natl. Inst. Health Res., Southampton, UK

10.1038/gim.2013.29

10.1002/ajmg.a.36298

10.1016/j.placenta.2004.10.017

10.1159/000279626

10.1002/pd.637

10.1097/MOP.0000000000000145

10.1007/s10897-009-9249-5

10.1503/cmaj.101368

10.1007/s10897-013-9673-4

10.1007/s10897-013-9590-6

10.1037/e584032011-022

91. Igenomix. 2015.NACE®:Non-Invasive Analysis for Chromosomal Examination.http://nace.igenomix.com/wp-content/uploads/NACE-specialists-EN.pdf

92. Illumina. 2015.Noninvasive prenatal testing—accurate information for your patients.http://www.illumina.com/clinical/reproductive-genetic-health/healthcare-professionals/non-invasive-prenatal-testing.html

93. Illumina. 2015.The reassurance of knowing.http://www.illumina.com/content/dam/illumina-marketing/documents/applications/reproductive-health/22336_LB_0013_G_Physician_Brochure.pdf

10.1136/bmj.f1957

10.1038/nm0413-381

10.1159/000367626

10.1080/01443610220130508

98. Kalantry S. 2014.Replacing myths with facts: sex-selective abortion laws in the United States. Cornell Leg. Stud. Res. Pap. 14-34, Cornell Law Sch., Ithaca, NY

10.1353/ken.2013.0017

100. Karow J. 2014. Premaitha to launch first CE IVD noninvasive prenatal test in Europe in early 2015.GenomeWeb, July 16.https://www.genomeweb.com/sequencing/premaitha-launch-first-ce-ivd-noninvasive-prenatal-test-europe-early-2015

101. Karow J. 2014. Sequenom to launch VisibiliT for average-risk pregnancies outside US, expand MaterniT21 Plus.GenomeWeb, July 23.https://www.genomeweb.com/sequencing/sequenom-launch-visibilit-average-risk-pregnancies-outside-us-expand-maternit21

10.1136/bmj.f3788

10.1097/AOG.0b013e3181a9479e

10.1007/s10897-014-9694-7

10.1038/491033a

106. Kittay EF, Kittay L. 2000. On the expressivity and ethics of selective abortion for disability: conversations with my son. See Ref. 148, pp. 165–95

10.1126/scitranslmed.3004323

10.1007/s10897-014-9758-8

10.1016/j.ajog.2006.09.013

10.1002/pd.2880

10.1002/ajmg.a.36226

Lampret JC, 2007, S. Afr. Med. J., 97, 515

10.1002/pd.4076

10.1002/pd.4124

115. LifeCodexx. 2014.PraenaTest®now starting at EUR 595.http://lifecodexx.com/wp-content/uploads/2015/03/WM-1097-EN-001_PraenaTest_is-now-starting_at_595EUR_Newsletter_July_2014_SCREEN.pdf

116. LifeCodexx. 2015.PrenaTest®.http://lifecodexx.com/en/expectant-mothers/prenatest

Lippman A, 1994, Women and Prenatal Testing: Facing the Challenges of Genetic Technology, 9

10.1126/scitranslmed.3001720

10.1016/S0140-6736(97)02174-0

10.1038/gim.2013.126

10.1002/ajmg.a.34054

10.1002/(SICI)1097-0223(199909)19:9<808::AID-PD637>3.0.CO;2-B

10.2217/pme.11.33

10.1038/gim.2013.142

10.1080/14636778.2013.822174

126. Maron DF. 2014. Virtual doctor visits gaining steam in “geneticist deserts.”Sci. Am., Apr. 21.http://www.scientificamerican.com/article/virtual-doctor-visits-gaining-steam

10.1002/ajmg.10006

10.1186/1750-1172-4-9

10.1002/pd.4127

10.1002/pd.4410

10.1038/gim.2014.101

10.1038/gim.2012.102

133. Minist. Health Fam. Welf. 2005.Annual report on implementation of the Pre-Conception and Pre-Natal Diagnostic Techniques(Prohibition of Sex Selection)Act.Rep., Minist. Health Fam. Welf., Gov. India, New Delhi

10.1038/sj.ejhg.5201956

10.1016/j.jdeveco.2013.02.007

136. Natera. 2015.About Panorama™.http://www.panoramatest.com/healthcare-provider

137. Natera. 2015.FAQs.http://www.panoramatest.com/en/expecting-mother/faqs

138. Natl. Coalit. Health Prof. Educ. Genet. 2012.Non-invasive prenatal testing(NIPT)factsheet.http://www.nchpeg.org/index.php?option=com_content&view=article&id=384&Itemid=255

10.1002/pd.2910

10.1002/pd.4103

10.1093/bmb/ldr015

10.1097/AOG.0b013e31828642c6

10.1177/1049732309335605

10.1016/j.pec.2008.09.020

10.1002/pd.4100

10.3138/chr.92.4.637

10.2307/3527746

Parens E, 2000, Prenatal Testing and Disability Rights

10.1002/mrdd.10056

10.1097/AOG.0000000000000363

151. Pinghui Z. 2014. Zhejiang man arrested for arranging sex tests in Hong Kong for pregnant mainland women.South China Morning Post, Apr. 18.http://www.scmp.com/news/china/article/1486420/zhejiang-man-arrested-arranging-sex-tests-hong-kong-pregnant-mainland

10.1503/cmaj.080454

10.1136/bmj.324.7348.1233/a

154. Pollack A. 2012. Conflict potential seen in genetic counselors.New York Times, July 13.http://www.nytimes.com/2012/07/14/business/conflict-potential-seen-in-genetic-counselors-paid-by-testing-companies.html

10.1007/s10897-011-9471-9

10.1159/000263878

10.1016/S0277-9536(97)00011-7

Rapp R, 1999, Testing Women, Testing the Fetus: The Social Impact of Amniocentesis in America

159. Ray. 2013. Amid “chaos,” FDA's Gutierrez offers insights on agency's regulatory stance on molecular tests.GenomeWeb, Feb. 12.https://www.genomeweb.com/clinical-genomics/amid-chaos-fdas-gutierrez-offers-insights-agencys-regulatory-stance-molecular-te

10.1016/j.socscimed.2004.02.016

10.1007/s10897-005-0573-0

10.1177/00224669020360010501

10.1002/pd.4052

10.1002/ajmg.a.36613

165. Saxton M. 2000. Why members of the disability community oppose prenatal diagnosis and selective abortion. See Ref. 148, pp. 147–64

10.1126/scitranslmed.3003612

10.1111/j.1467-8519.2008.00674.x

10.1016/S0140-6736(11)61786-8

169. Sequenom Lab. 2015.MaterniT21®PLUS.https://laboratories.sequenom.com/providers/maternit21-plus

170. Sequenom Lab. 2015.The science of revolutionizing prenatal care.http://flipbooks.sequenom.com/i/356741-mt21plus-microdeletions-essii-4-pg-brochure-070814-final-31-20241r1-0

171. Sequenom Lab. 2015.The VisibiliT™prenatal test.https://laboratories.sequenom.com/providers/visibilit

10.1007/s10897-011-9375-8

10.1016/B978-1-4377-1935-2.00010-7

10.1016/B978-1-4377-1935-2.00011-9

10.1016/j.ajog.2004.11.001

10.1136/adc.2009.166017

10.1002/ajmg.a.33082

10.1002/ajmg.a.34293

10.1002/ajmg.a.34235

180. Soc. Matern.Fetal Med. 2014.SMFM statement: maternal serum cell-free DNA screening in low risk women.https://www.smfm.org/publications/157-smfm-statement-maternal-serum-cell-free-dna-screening-in-low-risk-women

10.3109/14767058.2013.770464

10.1002/pd.4160

183. Spec. Olymp. 2005.Changing attitudes changing the world: the health and health care of people with intellectual disabilities.Policy Pap., Spec. Olymp., Washington, DC

184. Steinbock B. 2000. Disability, prenatal testing, and selective abortion. See Ref. 148, pp. 108–23

10.3109/14767058.2013.820699

10.1007/s10897-013-9684-1

10.1016/S0738-3991(00)00146-4

10.1016/S1701-2163(15)30441-2

189. Transpar. Mark. Res. 2014.Non-invasive prenatal testing(NIPT)market(MaterniT21 PLUS, verifi, Harmony, Panorama, NIFTY, PrenaTest and BambniTest)—global industry analysis, size, share, growth, trends and forecast, 2013–2019.Rep., Transpar. Mark. Res., Albany, NY

10.3109/14767058.2013.806477

10.1016/j.pec.2009.05.014

Van Zimmerman E, 2014, Breast Cancer Gene Research and Medical Practices: Transnational Perspectives in the Time of BRCA, 151

10.1097/AOG.0000000000000237

10.1186/1755-8166-7-33

10.1002/pd.3863

196. Wertz DC. 2000. Drawing lines: notes for policymakers. See Ref. 148, pp. 261–87

Willems PJ, 2014, Facts Views Vis. ObGyn, 6, 7

10.1054/midw.2002.0316

10.1007/s10897-012-9545-3

10.1002/pd.3946