This experiment has become a serious issue for two reasons: DNA methylation plays an important role during embryogenesis, global abnormal methylome reprogramming often occurs in human embryos, and DNA methylome pattern is associated with live birth rate. The endocrine metabolic disorders of polycystic ovarian syndrome (PCOS) patients may affect the epigenetic status of embryos and lead to the increase of early pregnancy loss rate in PCOS patients. However, there is still no technology using DNA methylome as an indicator in preimplantation embryo screening in PCOS patients. Our recent study showed that using Pre-implantation Methylation Screening (PIMS) can select embryos with better methylation state and euploid chromosomes. The efficiency of PIMS in PCOS patients needs further validation through randomized controlled clinical trial. The purpose of the study is to compare whether the two groups of PCOS patients who selected embryos using PIMS and selected embryos using "PGT-A + morphology"had any difference in early pregnancy loss rate. This study aims to explore whether PIMS can be used as another embryo evaluation method besides "PGT-A+morphology" to screen good developmental potential embryos in patients with PCOS. Investigators need to clarify whether a better embryo evaluation system can be established through PIMS technology during assisted reproductive treatment for infertile PCOS couples and provide credible and effective evidence-based medical evidence for the application of PMIS technology in the field of reproductive medicine.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
SCREENING
Masking
SINGLE
Enrollment
766
Couples in the PIMS group will have up to 6 blastocysts screened with PIMS and a single euploid embryo with the optimal state of whole-genome DNA methylation and the highest morphologic score will be selected for the initial transfer
Couples in the PGT-A group will have up to 6 blastocysts screened with PGT-A and a single euploid blastocyst with the highest morphologic score selected for the initial transfer.
early pregnancy loss rate
early pregnancy loss rate in one year after randomization
Time frame: From enrollment to the end of treatment at 12months
cumulative live birth rate per oocyte retrieval cycle
cumulative live birth rate per oocyte retrieval cycle in one year after randomization
Time frame: From enrollment to the end of treatment at 12months
clinical pregnancy rate after initial embryo transfer
Time frame: From enrollment to the end of treatment at 12months
time to get live birth
Time frame: From enrollment to the end of treatment at 12months
the rate of a Good Birth Outcome
Time frame: From enrollment to the end of treatment at 12months
multiple pregnancy rate
Time frame: From enrollment to the end of treatment at 12months
duration of pregnancy
Time frame: From enrollment to the end of treatment at 12months
birth weight
Time frame: From enrollment to the end of treatment at 12months
incidence of maternal and neonatal complications (including fetal anomalies)
Time frame: From enrollment to the end of treatment at 12months
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