Ethical Aspects of Prenatal DNA Testing

Author:

Stanić Žana12,Hrgović Zlatko3,Fureš Rajko12,Vusić Iva4,Lagančić Marko5

Affiliation:

1. Department for Integrative Gynecology, Obstetrics and Minimally Invasive Gynecologic Surgery, Zabok General Hospital and Croatian Veterans Hospital, Zabok, Croatia

2. Faculty of Dental Medicine and Health, Josip Juraj Strossmayer University of Osijek, Osijek, Croatia

3. Women's Health Clinic, J. W. Goethe University Frankfurt, Frankfurt am Main, Germany

4. Health Center of Bjelovar-Bilogora County, Bjelovar, Croatia

5. Emergency Department, University Hospital Dubrava, Zagreb, Croatia

Abstract

AbstractCell-free DNA (cfDNA) first-trimester screening for fetal aneuploidies, as a non-invasive, safe, and rather accurate method, has changed prenatal screening policies all over the world. Owing to aggressive marketing, cfDNA screening tests exhibit global popularity and a rapid spread in routine prenatal care. However, wide availability of the tests, together with observed difficulties in the test’s interpretation, bring to light several serious ethical concerns. To date it is vital to identify and address the most important ethical, legal, and social issues regarding prenatal screening tests. Furthermore, guidelines and restrictions in certain cfDNA screening advancements that may provide information regarding fetal genetic traits of unknown clinical significance, conditions with variable penetrance, or late-onset conditions, should be considered.

Publisher

Georg Thieme Verlag KG

Subject

Maternity and Midwifery,Obstetrics and Gynecology,Pediatrics, Perinatology and Child Health

Reference52 articles.

1. Noninvasive prenatal testing goes global;S Chandrasekharan;Sci Transl Med,2014

2. First trimester serum tests for Down’s syndrome screening;S K Alldred;Cochrane Libr,2015

3. Prenatal screening for fetal aneuploidy in singleton pregnancies;D Chitayat;J Obstet Gynaecol Can,2011

4. Noninvasive chromosomal evaluation (NICE) study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18;M E Norton;Am J Obstet Gynecol,2012

5. DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study;G E Palomaki;Gen Med,2012

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