Non-invasive prenatal diagnosis for translocation carriers—YES please or NO go?
Acta Obstetricia et Gynecologica Scandinavica , Volume 100 - Issue 11 p. 2036- 2043
<p>Introduction: The presence of an unbalanced familial translocation can be reliably assessed in the cytotrophoblast of chorionic villi. However, carriers of a balanced translocation often decline invasive testing. This study aimed to investigate whether an unbalanced translocation can also be diagnosed in cell free DNA by whole-genome non-invasive prenatal screening (NIPS). Material and methods: Pregnant women carrying a fetus with an unbalanced familial translocation, for whom NIPS as well as microarray data were available, were included in this retrospective assessment. NIPS was performed in the course of the TRIDENT study. Results: In 12 cases, both NIPS and microarray data were available. In 10 of 12 cases the unbalanced translocation was correctly identified by NIPS without prior knowledge on parental translocation. One was missed because the fetal fraction was too low. One was missed because of technical restrictions in calling 16p gains. Conclusions: This study supports the hypothesis that routine NIPS may be used for prenatal diagnosis of unbalanced inheritance of familial translocations, especially with prior knowledge of the translocation allowing focused examination of the involved chromosomal regions. Our study showed that routine shallow sequencing designed for aneuploidy detection in cell free DNA may be sufficient for higher resolution NIPS, if specialized copy number software is used and if sufficient fetal fraction is present.</p>
|Acta Obstetricia et Gynecologica Scandinavica|
|Organisation||Erasmus MC: University Medical Center Rotterdam|
M.I. (Gosia) Srebniak, F.M. (Fernanda) Jehee, M. (Marieke) Joosten, M. (Marjan) Boter, WG (Walter) de Valk, R.M. (Robert) van der Helm, … A.R.M. (Diane) van Opstal. (2021). Non-invasive prenatal diagnosis for translocation carriers—YES please or NO go?. Acta Obstetricia et Gynecologica Scandinavica, 100(11), 2036–2043. doi:10.1111/aogs.14256