Abstract

BackgroundHuman menopausal gonadotrophins and recombinant human follicle stimulating hormone are the two main gonadotrophin products utilized for controlled ovarian stimulation in assisted reproductive technologies. In this meta-analysis, the number of oocytes was designated as the most relevant endpoint directly resulting from ovarian stimulation, and therefore where the drug effect may be estimated with the best sensitivity.MethodsAll published randomized controlled trials on ovarian stimulation comparing the two gonadotrophin products were evaluated. Internal validity was determined using Chalmers' validated scale. If trials did not meet the established quality criteria, a sensitivity analysis assessed the stability of the results. The comparison of continuous variables was conducted following the weighted mean difference and the standardized mean difference (Cohen's effect size) with the random model. Given the known relationship of baseline conditions on treatment endpoints, results were adjusted for age, body mass index and type of infertility.ResultsSixteen studies involving 4040 patients were included. Treatment with human menopausal gonadotrophins resulted in fewer oocytes (-1.54; 95% CI: -2.53 to -0.56; P < 0.0001) compared to recombinant human follicle-stimulating hormone. When adjusting for baseline conditions, the mean difference estimate was -2.10 (95% CI: -2.83 to -1.36; P < 0.001). A higher total dose of human menopausal gonadotrophin was necessary (mean difference, 235.46 IU [95% CI: 16.62 to 454.30; P = 0.03]; standardized mean difference, 0.33 [95% CI: 0.08 to 0.58; P = 0.01]). The pregnancy absolute risk difference (RD [hMG-r-hFSH]) for fresh transfers was 3% (P = 0.051), and the relative risk 1.10 (P = 0.06). When adjusted for baseline conditions, the relative risk was 1.04 (P = 0.49) and absolute difference was 0.01 (P = 0.34), respectively.ConclusionsBecause baseline conditions are predictive of outcome, meta-analytic results are more sensitive when these variables are considered. Using an endpoint closely associated with the stimulation period, sufficient sensitivity is achieved to compare gonadotrophin treatments. As the largest meta-analysis published to date on this subject, treatment with human menopausal gonadotrophins is characterized by fewer oocytes and a higher total dose. When considering only fresh transfers, pregnancy rates were similar.

Highlights

  • Human menopausal gonadotrophins and recombinant human follicle stimulating hormone are the two main gonadotrophin products utilized for controlled ovarian stimulation in assisted reproductive technologies

  • R-hFSH and hMG are two of the gonadotrophin products primarily used for controlled ovarian stimulation (COS) in Assisted Reproduction Techniques (ART), including in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI)

  • Identification of literature All publications related to randomized controlled trials (RCTs) comparing COS with hMG and recombinant human follicle stimulating hormone (r-hFSH) were identified using the Cochrane Library’s Cochrane Menstrual Disorders and Subfertility Review Group specialized register of controlled trials and the Cochrane Central Register of Controlled Trials as well as MEDLINE and EMBASE databases using the following key words and/or medical subject heading (MeSH) terminology: follicle stimulating hormone, FSH, r-hFSH, hMG, recombinant human luteinizing hormone, recombinant human chorionic gonadotrophin (hCG), OHSS, randomized controlled trial, controlled clinical

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Summary

Introduction

Human menopausal gonadotrophins and recombinant human follicle stimulating hormone are the two main gonadotrophin products utilized for controlled ovarian stimulation in assisted reproductive technologies. R-hFSH and hMG are two of the gonadotrophin products primarily used for controlled ovarian stimulation (COS) in Assisted Reproduction Techniques (ART), including in vitro fertilization (IVF) and intracytoplasmic sperm injection (ICSI). Both hMG and r-hFSH have been shown to be effective, a number of studies have further compared their safety and clinical effectiveness [1,2,3,4,5,6]. Other authors have reported better COS outcomes with r-hFSH in terms of a lower total r-hFSH dose compared with urine-derived gonadotrophins, and an increased number of follicles, oocytes, embryos and/or pregnancies [3,4,5,6]

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