# Luteal-phase stimulation does not compromise embryo euploidy or live birth outcomes compared to follicular-phase stimulation

**Authors:** Boyuan Chen, Meiling Zhang, Min Wang, Yong Wang, Xiaojun Chen, Li Wang, Wen Li, Dandan Wu

PMC · DOI: 10.3389/fmed.2026.1722250 · Frontiers in Medicine · 2026-02-11

## TL;DR

This study found that luteal-phase stimulation in IVF does not reduce embryo quality or live birth rates compared to the traditional follicular-phase stimulation.

## Contribution

The study provides evidence that luteal-phase stimulation is as effective as follicular-phase stimulation in terms of embryo euploidy and live birth outcomes.

## Key findings

- Luteal-phase stimulation had similar euploidy rates compared to follicular-phase stimulation.
- Live birth rates were comparable between the two stimulation protocols.
- Luteal-phase stimulation resulted in fewer retrieved oocytes but did not compromise reproductive outcomes.

## Abstract

Aneuploidy is a major cause of implantation failure and miscarriage in assisted reproductive technology. This study aimed to evaluate embryo euploidy and live birth rates associated with the luteal-phase stimulation (LPS) protocol in in vitro fertilization (IVF), compared with the follicular-phase stimulation (FPS) protocol.

We conducted a retrospective cohort study at a university-affiliated fertility center, including 667 preimplantation genetic testing for aneuploidy (PGT-A) cycles performed between January 2020 and June 2023. After 1:1 propensity score matching, 106 cycles were analyzed from each group (LPS and FPS). Baseline characteristics, ovarian stimulation parameters, euploidy rate, and subsequent reproductive outcomes were compared.

After matching, baseline characteristics were comparable between the groups. The LPS group required a longer duration of gonadotropin stimulation (median 10.5 vs. 9 days, p < 0.001) and yielded fewer retrieved oocytes (median 6 vs. 9, p < 0.05) than the FPS group. On the day of hCG administration, patients in the LPS group had significantly higher progesterone levels than those in the FPS group (median 6.1 vs. 3.1, p < 0.001). However, the euploidy rate did not differ significantly (33.9% vs. 30.8%, p > 0.05). Subgroup analyses stratified by age (<38 and ≥38 years) revealed consistent results. Similarly, the clinical pregnancy rate (55.9% vs. 64.1%, p > 0.05), live birth rate (41.2% vs. 46.2%, p > 0.05), and pregnancy loss rate (14.7% vs. 17.9%, p > 0.05) after the first embryo transfer were comparable.

The LPS protocol demonstrated similar embryo euploidy and live birth rates to the FPS protocol, suggesting that LPS does not compromise chromosomal competence or reproductive outcomes. However, the lower oocyte yield in the LPS group could potentially affect cumulative pregnancy and live birth rates. Given its scheduling flexibility, LPS may still represent a clinically feasible and patient-friendly option in assisted reproductive technology (ART).

## Full-text entities

- **Genes:** HTC2 (hypertrichosis 2 (generalized, congenital)) [NCBI Gene 3342] {aka CGH, CXINSq27.1, HCG}, AMH (anti-Mullerian hormone) [NCBI Gene 268] {aka MIF, MIS}, CGB5 (chorionic gonadotropin subunit beta 5) [NCBI Gene 93659] {aka CGB, HCG}, GNRH1 (gonadotropin releasing hormone 1) [NCBI Gene 2796] {aka GNRH, GRH, LHRH, LNRH}
- **Diseases:** monogenic disease (MESH:D004194), ectopic pregnancy (MESH:D011271), menstrual cycle disorder (OMIM:614674), monogenic disorders (MESH:D009358), birth (MESH:D000014), OHSS (MESH:D016471), abortion (MESH:D000026), Pregnancy loss (MESH:D000022), Aneuploidy (MESH:D000782), IVF (MESH:C566179), PPOS (MESH:D010049)
- **Chemicals:** MPA (MESH:D017258), E2 (MESH:D004958), HMG (MESH:D008596), progesterone (MESH:D011374), letrozole (MESH:D000077289), FPS (-), Utrogestan (MESH:C000624167), Duphaston (MESH:D004394), Crinone (MESH:C400424), LH (MESH:D007986)
- **Species:** Homo sapiens (human, species) [taxon 9606], Halomonas sp. MG (species) [taxon 1729644]

## Full text

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## Figures

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## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12932428/full.md

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Source: https://tomesphere.com/paper/PMC12932428