Peptides DB
Research-centric peptide and protocol reference hub
Study 2 of 3Buserelin literatureAnnals of medicine · Observational2026

Oocyte maturation and pregnancy outcomes in relation to gonadotropin duration in antagonist cycles.

Gn stimulation duration significantly affects oocyte maturation, with an optimal window of 8-10 days linked to better pregnancy outcomes.

Read at Annals of medicineAdd to compare

Where it sits

this study against the rest of the buserelin corpus
0
Preclinical
3
Observational · this one
0
Open-label
0
Randomised
0
Reviews

Summary and findings

This study evaluated the association between gonadotropin (Gn) stimulation duration and oocyte maturation and pregnancy outcomes in 9372 GnRH antagonist cycles. The analysis found that Gn duration had a significant nonlinear association with oocyte maturation, with an optimal duration of 8-10 days linked to higher pregnancy likelihood. No therapeutic claims are made.

How much of this paper we could read: full text read (0.90). We had a clear abstract, so the summary below closely tracks the paper. What this means →
Adjusted OR 1.07 for oocyte maturation per day of Gn stimulation, 95% CI 1.05-1.09, p<0.001.n=93722026

Abstract

The authors’ words, as Annals of medicine supplied them

<h4>Objective</h4>Gonadotropin (Gn) stimulation duration is a modifiable factor in antagonist protocols, yet its association with oocyte maturation and pregnancy outcomes remains unclear. This study aimed to determine whether Gn duration is independently associated with oocyte maturation and pregnancy outcomes after controlling for key confounders and to identify an optimal Gn window in GnRH antagonist cycles with fresh embryo transfer.<h4>Methods</h4>This retrospective study included 9372 GnRH antagonist cycles at Xiangya Hospital. Multivariable regression models adjusting for confounders were used to assess the associations of Gn duration with oocyte maturation and pregnancy outcomes. Subgroup analyses were stratified by ovarian response. Generalized additive models were employed to identify nonlinear trends, followed by segmented and LOESS regression to determine the optimal duration.<h4>Results</h4>After comprehensive adjustment, Gn duration maintained a significant nonlinear association with oocyte maturation (adjusted OR 1.07, 95% CI 1.05-1.09, <i>p</i> < .001), plateauing at approximately 9 days. Each additional stimulation day before 9 days was associated with increased maturation odds (adjusted OR 1.11, 95% CI 1.06-1.17; <i>p</i> < .001), while extended duration beyond 9 days showed no significant benefit (adjusted OR 0.94, 95% CI 0.88-1.01; <i>p</i> = .08). This association was absent in very low responders (≤5 oocytes) but consistent across other response subgroups. The 8-10 day duration window was associated with the highest likelihood of pregnancy and live birth.<h4>Conclusion</h4>In GnRH antagonist cycles, Gn duration is associated with oocyte maturation and pregnancy outcomes following fresh embryo transfer, even after adjusting for key confounders. The 8-10 day Gn window represents a range associated with the highest likelihood of clinical pregnancy and live birth. These findings support prioritizing dynamic, response-adapted stimulation protocols aimed at achieving trigger criteria within this window, rather than adhering to fixed duration targets.

Background

This paper addresses the relationship between gonadotropin stimulation duration and its effects on oocyte maturation and pregnancy outcomes in GnRH antagonist cycles. Previous studies have suggested that Gn duration may influence these outcomes, but the optimal duration remains unclear. Understanding this relationship is crucial for optimizing fertility treatment protocols.

Methods

The study utilized a retrospective design, analyzing 9372 GnRH antagonist cycles from Xiangya Hospital. Multivariable regression models were employed to control for confounders, and generalized additive models were used to assess nonlinear associations. The primary outcomes included oocyte maturation rates and pregnancy outcomes following fresh embryo transfer.

Results

The primary endpoint indicated that Gn duration had a significant nonlinear association with oocyte maturation, with an adjusted OR of 1.07 (95% CI 1.05-1.09, p<0.001). Each additional day of stimulation before 9 days increased maturation odds (adjusted OR 1.11, 95% CI 1.06-1.17; p<0.001), while extending beyond 9 days showed no significant benefit (adjusted OR 0.94, 95% CI 0.88-1.01; p=0.08).

Interpretation

These findings suggest that while there is a statistically significant association between Gn duration and oocyte maturation, the clinical significance of extending Gn beyond 9 days is questionable. The absence of association in very low responders and the reliance on a single-site retrospective design may limit the generalizability of the results. This study adds to the existing literature by identifying an optimal duration window for Gn stimulation.

Key findings

  • Adjusted OR 1.07 for oocyte maturation per day of Gn stimulation, 95% CI 1.05-1.09, p<0.001.
  • Each additional stimulation day before 9 days increased maturation odds (adjusted OR 1.11, 95% CI 1.06-1.17; p<0.001).
  • Extended duration beyond 9 days showed no significant benefit (adjusted OR 0.94, 95% CI 0.88-1.01; p=0.08).
  • The 8-10 day Gn duration window was associated with the highest likelihood of pregnancy and live birth.
  • Association absent in very low responders (≤5 oocytes).

Limitations

  • Retrospective study design.
  • Single-site analysis.
  • Potential residual confounding despite adjustments.
  • No data on long-term outcomes.

Elsewhere in the Buserelin corpus

BRestoring ovulation in functional hypothalamic amenorrhea: impact of polycystic ovarian morphology on hormonal response to pulsatile GnRH.Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology · 2026 · n=41 · Median AMH levels at baseline were 6.21 ng/ml in the PCOM group vs 1.7 ng/ml in the non-PCOM group, p<0.001.HumanBEfficacy and safety of combined GnRH-a, hysteroscopic surgery, and LNG-IUS for adenomyosis with suboptimal HIFU ablation: a retrospective study.International journal of hyperthermia : the official journal of European Society for Hyperthermic Oncology, North American Hyperthermia Group · 2026 · n=71 · Median NPV ratio following HIFU ablation was 22.2% (IQR: 12.0%-36.2%)Human