Capacitation in vitro maturation (CAPA-IVM) has improved oocyte maturation and resulted in live births. Because cumulus cells (CCs) communicate bidirectionally with the oocyte, their transcriptomic profile may serve as a non-invasive biomarker of oocyte and embryo competence. This prospective pilot study will analyze CCs gene expression after CAPA-IVM using RNA sequencing and pathway analysis, and correlate findings with embryological outcomes including fertilization, day-3 cleavage, and blastocyst formation. Results are expected to provide insights into the molecular basis of oocyte competence and support development of non-invasive embryo selection strategies.
In vitro maturation (IVM) is an alternative to conventional ovarian stimulation, particularly for women with polycystic ovary syndrome (PCOS) or at risk of ovarian hyperstimulation syndrome (OHSS). A novel technique, known as capacitation IVM (CAPA-IVM), introduces a pre-maturation step that improves both nuclear and cytoplasmic maturation and has been associated with live births. Cumulus-oocyte complexes (COCs) represent the functional unit of oocyte competence, with cumulus cells (CCs) providing bidirectional signaling that regulates oocyte development. Because CCs are routinely removed during ICSI, they serve as a readily accessible and non-invasive source of information about oocyte and embryo potential. This prospective observational cohort study will be conducted at the IVFMD, My Duc Hospital, Ho Chi Minh City, Vietnam. Eligible participants are women diagnosed with PCOS according to the Rotterdam 2003 criteria, with serum AMH ≥ 4 ng/mL and antral follicle count (AFC) ≥ 24, indicated for CAPA-IVM treatment. From each participant, 15 COCs will be allocated to single-culture CAPA-IVM condition. CCs from each COC will be collected for transcriptomic analysis, while the oocytes are assessed for embryological outcomes. The remaining COCs will follow the standard CAPA-IVM protocol at the center. RNA sequencing will be performed using low-input protocols. Data will undergo differential expression analysis (DESeq2), and functional interpretation using Gene Ontology and Ingenuity Pathway Analysis. Laboratory outcomes including day-3 cleavage, and blastocyst formation will be correlated with CC transcriptomic profiles. This study aims to identify non-invasive biomarkers of oocyte and embryo competence, supporting future embryo selection strategies in assisted reproduction. By correlating cumulus cell transcriptomic profiles with oocyte and embryo outcomes, this study seeks to establish preliminary non-invasive biomarkers for embryo selection in assisted reproduction.
Study Type
OBSERVATIONAL
Enrollment
10
My Duc Hospital
Ho Chi Minh City, Vietnam
RECRUITINGCorrelation of cumulus cell transcriptomic profiles with embryological outcomes
Association between cumulus cell gene expression (RNA-seq-based transcriptomic profiles) and embryological outcomes, including cleavage and embryo quality (Day 3), and blastocyst formation and grading (Days 5-6).
Time frame: Through study completion, an average of 1 year
CCs transcriptomic profiles
RNA sequencing of CCs collected from individual COCs after CAPA-IVM. Differential gene expression will be analyzed using DESeq2, followed by Gene Ontology enrichment and Ingenuity Pathway Analysis to identify pathways, molecular functions, and regulatory networks associated with oocyte competence.
Time frame: Through study completion, an average of 1 year
Number of matured oocyte
The number of oocytes that have first polar body after denudation
Time frame: At day 2 after the Oocyte Pick-Up day
Number of normal fertilized oocytes
Oocytes that show the presence of two pronuclei
Time frame: 16-18 hours after intracytoplasmic sperm injection
Number of day-3 embryos
Day-3 embryo morphology assessed according to the Istanbul Consensus (2011), with reference to the revised criteria (2024)
Time frame: 68 ±1 hours after intra-cytoplasmic sperm injection
Number of good-quality day-3 embryos
Day-3 embryo morphology assessed according to the Istanbul Consensus (2011), with reference to the revised criteria (2024)
Time frame: 68±1 hours after intra-cytoplasmic sperm injection
Number of blastocyst
Blastocyst quality assessed on Day 5/6 according to the Istanbul Consensus (2011), with reference to the revised criteria (2024).
Time frame: Day 5 (116 ± 2 hours) and Day 6 (140 ± 2 hours) after intra-cytoplasmic sperm injection
Number of good-quality blastocyst
Good-quality blastocysts defined and graded according to the Istanbul Consensus (2011), with reference to the revised criteria (2024).
Time frame: Day 5 (116 ± 2 hours) and Day 6 (140 ± 2 hours) after intracytoplasmic sperm injection
Number of frozen embryos
Embryos that meet morphology and developmental criteria for cryopreservation by vitrification
Time frame: At the time of embryo cryopreservation
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.