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Updated: Jan 17, 2026

Semiconductor Sequencing for Preimplantation Genetic Testing for Aneuploidy
Published on: August 25, 2019
Controlled Ovarian Stimulation Contributes to the Incidence of de Novo Chromosomal Abnormalities in Cleavage-Stage
Yinghui Ye1, Jieliang Ma2, Qitao Zhan1
1Department of Reproductive Endocrinology, Women's Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Background:
Studies on the effects of ovarian stimulation on the embryo aneuploidy rate have shown conflicting results.
Objectives:
To investigate whether parameters of controlled ovarian stimulation (COS) are associated with the incidence of de novo chromosomal abnormalities in cleavage-stage embryos undergoing preimplantation genetic testing (PGT).
Methods:
This retrospective study examined data from biopsies of cleavage-stage embryos with one blastomere from the Women's Hospital at Zhejiang University School of Medicine. De novo chromosomal abnormalities were classified as: de novo chromosomal segmental abnormalities (DCSAs) or de novo whole chromosomal abnormalities (DWCAs). A multivariable logistic regression model was used to identify factors that may affect the genomic stability of embryos. Further stratification analysis was performed to explore the impact of these factors on DCSAs and DWCAs.
Results:
A total of 1,994 cleavage-stage biopsied embryos were included in the analysis. The number of DWCAs but not DCSAs increased significantly with maternal age. The incidence of de novo chromosomal abnormalities was similar between different COS protocols. Longer stimulation duration was associated with a considerably higher DWCA rate (p = 0.003). The DCSA rate increased with higher gonadotropin dosages. Furthermore, cotreatment with growth hormone (GH) supplementation was associated with a significantly lower incidence of DWCAs (p = 0.006).
Conclusion:
Ovarian stimulation parameters are related to the incidence of de novo chromosomal abnormalities in preimplantation embryos. GH supplementation had a beneficial effect in decreasing aneuploidy, and higher gonadotropin doses may be related to mitotic errors.
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