Namath · Fertility and sterility 2025 · Retrospective cohort study · n=986

The number of autologous, vitrified mature oocytes needed to obtain three euploid blastocysts increases with age.

Cited 5 times in the scientific literature.

Level 3 - non-randomized controlled study

Retrospective multicenter cohort study

PubMed 40280226 · doi:10.1016/j.fertnstert.2025.04.023 · record verified 2026-08-26

What was done

This retrospective multicenter cohort study analyzed 1,041 oocyte thaw cycles from 986 patients who warmed autologous vitrified oocytes for in vitro fertilization between 2011 and October 2023. Patients were stratified by age at the time of vitrification to evaluate the number of mature (metaphase II [MII]) oocytes required to obtain at least three euploid blastocysts and to assess expected live births per thawed MII oocyte.

What was found

Patients aged <35 years at vitrification required a mean of 15 MII oocytes to achieve at least three euploid blastocysts. The required number of MII oocytes doubled in patients aged ≥38 years and tripled in patients aged >40 years. Expected live births per thawed MII oocyte were 0.13 for women <35 years versus 0.04 for women >40 years at vitrification. Patients aged 35–40 years utilized preimplantation genetic testing more frequently than those <35 or >40 years. Age at vitrification was more predictive of expected live birth outcomes than the specific clinical indication for cryopreservation.

Why it matters

These findings provide concrete, age-stratified targets for fertility preservation counseling, demonstrating that patients banking eggs at or after age 38 will generally require multiple retrieval cycles to accumulate enough mature oocytes for a high cumulative live birth probability.

Limits

The study is limited by its retrospective design and potential selection bias regarding which patients chose to thaw oocytes and pursue preimplantation genetic testing. The primary endpoint relied on achieving three euploid blastocysts as a surrogate for live birth rather than complete per-transfer pregnancy follow-up for every generated embryo. Clinical protocols and laboratory vitrification techniques may have also shifted across the 12-year study window.

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