Abstract

This prospective study evaluated the accuracy of non-invasive preimplantation genetic testing for aneuploidy (niPGT-A) using cell-free DNA in spent culture medium, as well as that of preimplantation genetic testing for aneuploidy (PGT-A) using trophectoderm (TE) biopsy after culturing beyond implantation. Twenty frozen blastocysts donated by 12 patients who underwent IVF at our institution were investigated. Of these, 10 were frozen on day 5 and 10 on day 6. Spent culture medium and TE cells were collected from each blastocyst after thawing, and the embryos were cultured in vitro for up to 10 days. The outgrowths after culturing beyond implantation were sampled and subjected to chromosome analysis using next-generation sequencing. Chromosomal concordance rate, sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), false-positive rate (FPR), and false-negative rate (FNR) of niPGT-A and PGT-A against each outgrowth were analyzed. The concordance rate between the niPGT-A and outgrowth samples was 9/16 (56.3%), and the concordance rate between the PGT-A and outgrowth samples was 7/16 (43.8%). NiPGT-A exhibited 100% sensitivity, 87.5% specificity, 88.9% PPV, 100% NPV, 12.5% FPR, and 0% FNR. PGT-A exhibited 87.5% sensitivity, 77.8% specificity, 87.5% PPV, 75% NPV, 14.3% FPR, and 22.2% FNR. NiPGT-A may be more accurate than PGT-A in terms of ploidy diagnostic accuracy in outgrowths.

Highlights

  • Human embryos are prone to chromosomal abnormalities, primarily due to chromosome separation errors occurring during meiosis [1]

  • The culture time after removing the zona pellucida was different between the 5-day-old and 6-day-old embryos, there was no difference in the DNA concentration of the culture medium collected for non-invasive preimplantation genetic testing for aneuploidy (niPGT-A) (5-day-old embryo group: 22.0ng/μL vs. 6-day-old embryo group 19:22.3 ng/μL; p = 0.807)

  • Spent culture medium of the recovery culture from embryo thawing to TE biopsy was collected for niPGT-A, and the results of TE biopsies of preimplantation genetic testing for aneuploidy (PGT-A) samples were correlated with the outgrowth chromosomal status, respectively

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Summary

Introduction

Human embryos are prone to chromosomal abnormalities, primarily due to chromosome separation errors occurring during meiosis [1]. Chromosomal abnormalities can cause miscarriages in early pregnancy and many serious chromosomal disorders [2]. Cell-free DNA in medium reflects the chromosomal status of embryos after culture beyond implantation

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