4.3 Article

The impact of preimplantation genetic testing for aneuploidy on prenatal screening

Journal

JOURNAL OF PERINATAL MEDICINE
Volume 50, Issue 3, Pages 300-304

Publisher

WALTER DE GRUYTER GMBH
DOI: 10.1515/jpm-2021-0495

Keywords

aneuploidy screening; in vitro fertilization (IVF); preimplantation genetic testing for aneuploidy (PGT-A); prenatal diagnosis; serum analytes

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The study suggests that preimplantation genetic testing for aneuploidy (PGT-A) does not reduce the risk of abnormal prenatal screening results in singleton pregnancies conceived through in vitro fertilization. Rates of screening and diagnostic testing were similar between pregnancies conceived with PGT-A and those conceived without testing.
Objectives To determine whether preimplantation genetic testing for aneuploidy (PGT-A) is associated with a reduced risk of abnormal conventional prenatal screening results in singleton pregnancies conceived using in vitro fertilization (IVF). Methods This was a retrospective cohort study of singleton IVF pregnancies conceived from a single tertiary care center between January 2014 and September 2019. Exclusion criteria included mosaic embryo transfers, vanishing twin pregnancies, and cycles with missing outcome data. Two cases of prenatally diagnosed aneuploidy that resulted in early voluntary terminations were also excluded. The primary outcome of abnormal first or second-trimester combined screening results was compared between two groups: pregnancy conceived after transfer of a euploid embryo by PGT-A vs. transfer of an untested embryo. Multivariable backwards-stepwise logistic regression with Firth method was used to adjust for potential confounders. Results Of the 419 pregnancies included, 208 (49.6%) were conceived after transfer of a euploid embryo by PGT-A, and 211 (50.4%) were conceived after transfer of an untested embryo. PGT-A was not associated with a lower likelihood of abnormal first-trimester (adjusted OR 1.64, 95% CI 0.82-3.39) or second-trimester screening results (adjusted OR 0.96, 95% CI 0.56-1.64). The incidences of cell-free DNA testing, fetal sonographic abnormalities, genetic counseling, and invasive prenatal diagnostic testing were similar between the two groups. Conclusions Our data suggest that PGT-A is not associated with a change in the likelihood of abnormal prenatal screening results or utilization of invasive prenatal diagnostic testing. Counseling this patient population regarding the importance of prenatal screening and prenatal diagnostic testing, where appropriate, remains essential.

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