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Gonadorelin

GnRH, Luteinizing Hormone-Releasing Hormone, LHRH, Factrel

Quick Stats
Studies 192
Trials 100
Score 2
2025 pubmed

Nomogram-Based Prediction of Live Birth in GnRH Antagonist Protocol Fresh IVF/ICSI Cycles.

Zhong. Yanyu Y; Kang. Qian Q; Pang. Xin X; Wang. Nan N

Key Findings

  • A six‑parameter model (including progesterone on day 9 after egg retrieval, number of embryos transferred, and creatinine) predicts live‑birth odds in GnRH‑antagonist IVF cycles.
  • The model showed moderate accuracy in the training set (AUC 0.72) and higher accuracy in the validation set (AUC 0.81).
  • Decision‑curve analysis suggested the nomogram could help clinicians personalize IVF treatment decisions.

Practical Outcomes

  • For people interested in fertility optimization, the study offers a ready‑to‑use scoring chart that can estimate IVF success based on routine blood tests. It doesn’t change how gonadorelin is used, but it may help patients and clinicians decide how many embryos to transfer or whether to adjust protocols for better chances of a live birth.

Summary

Researchers built a simple calculator that uses six lab measurements (like progesterone levels and kidney function) to guess the chance of having a baby after a fresh IVF cycle that uses a GnRH‑antagonist drug regimen. The tool worked fairly well in the data they studied, especially when they tested it on a separate group.

Abstract

This investigation sought to determine optimal prognostic indicators and develop an implementable predictive framework for estimating live birth probabilities in subfertile individuals receiving gonadotropin-releasing hormone antagonist-based ovarian stimulation during fresh embryo transfer cycles of assisted reproductive technology. In this observational cohort analysis, we examined consecutive fresh in vitro fertilization/embryo transfer (IVF/ET) cycles utilizing GnRH antagonist protocols (training = 587, validation = 168 cycles; 2017-2022). Live birth rate served as the principal outcome measure. Through multivariable regression modeling, we identified key predictive variables and constructed a visual prediction tool. Model robustness was assessed using ROC-AUC metrics and decision curve validation with 500 bootstrap iterations. The final predictive algorithm incorporated six clinical parameters: serum progesterone on post-ovulation day 9 (serum P (OPU+9) ≥ 51.4 ng/mL), transferred embryo count, progesterone-follicle ratio (PFR), triggering-day progesterone levels, progesterone-to-total follicle ratio, and creatinine concentrations. The training cohort demonstrated moderate discriminative capacity (ROC-AUC 0.72, 95% CI 0.68-0.76), with enhanced performance in validation samples (AUC 0.81, 95% CI 0.73-0.89). Decision curve evaluations confirmed the model's clinical applicability. Our prognostic scoring chart offers an accessible and practical clinical instrument for estimating reproductive success in GnRH antagonist-based IVF/ICSI cycles. This tool facilitates personalized treatment planning and therapeutic strategy optimization, potentially improving resource allocation in fertility care.

Study Information

Provider

pubmed

Year

2025

Date

2025-11-05T00:00:00.000Z

DOI

10.2147/ijwh.s525614