Elevated early follicular progesterone levels and in vitro fertilization outcomes: a prospective intervention study and meta-analysis

Fertil Steril. 2014 Aug;102(2):448-454.e1. doi: 10.1016/j.fertnstert.2014.05.002. Epub 2014 Jun 11.

Abstract

Objective: To assess the impact of elevated early follicular progesterone (P) levels in gonadotropin-releasing hormone (GnRH) antagonist cycles on clinical outcome using prospective data in combination with a systematic review and meta-analysis.

Design: Nested study within a multicenter randomized controlled trial and a systematic review and meta-analysis.

Setting: Reproductive medicine center in an university hospital.

Patient(s): 158 in vitro fertilization/intracytoplasmic sperm injection (IVF-ICSI) patients.

Intervention(s): Recombinant follicle-stimulating hormone (FSH) (150-225 IU) administered daily from cycle day 2 onward; GnRH antagonist treatment randomly started on cycle day 2 or 6; assignment into two groups according to P level on cycle day 2: normal or elevated (>4.77 nmol/L or >1.5 ng/mL, respectively).

Main outcome measure(s): Ongoing pregnancy rate (OPR) per started cycle.

Result(s): The incidence of elevated P was 13.3%. A non-statistically-significant difference in OPR was present between the normal and elevated P groups (27.0% vs. 19.0%). No differential impact of early or late GnRH antagonist initiation on the effect of elevated or normal P on OPR was observed. A systematic search of Medline and EMBASE from 1972-2013 was performed to identify studies analyzing elevated early P levels in GnRH antagonists. The meta-analysis (n=1,052) demonstrated that elevated P levels statistically significantly decreased the OPR with 15% (95% CI -23, -7 %). Heterogeneity across the studies, presumably based on varying protocols, may have modulated the effect of elevated P.

Conclusion(s): From the present meta-analysis it appears that early elevated P levels are associated with a lower OPR in GnRH antagonists. The incidence of such a condition, however, is low.

Clinical trial registration number: NCT00866034.

Keywords: Clinical outcome; GnRH antagonist; IVF; progesterone levels.

Publication types

  • Meta-Analysis
  • Research Support, Non-U.S. Gov't
  • Review
  • Systematic Review

MeSH terms

  • Adult
  • Biomarkers / metabolism
  • Female
  • Fertility Agents, Female / administration & dosage*
  • Fertility Agents, Female / adverse effects
  • Fertilization in Vitro*
  • Follicle Stimulating Hormone / administration & dosage
  • Gonadotropin-Releasing Hormone / antagonists & inhibitors
  • Gonadotropin-Releasing Hormone / metabolism
  • Hormone Antagonists / administration & dosage
  • Humans
  • Infertility / diagnosis
  • Infertility / metabolism
  • Infertility / physiopathology
  • Infertility / therapy*
  • Netherlands
  • Ovarian Follicle / drug effects*
  • Ovarian Follicle / metabolism
  • Ovulation Induction / adverse effects
  • Ovulation Induction / methods*
  • Pregnancy
  • Pregnancy Rate
  • Progesterone / metabolism*
  • Randomized Controlled Trials as Topic
  • Recombinant Proteins / administration & dosage
  • Sperm Injections, Intracytoplasmic
  • Time Factors
  • Treatment Outcome
  • Up-Regulation

Substances

  • Biomarkers
  • Fertility Agents, Female
  • Hormone Antagonists
  • Recombinant Proteins
  • Gonadotropin-Releasing Hormone
  • Progesterone
  • Follicle Stimulating Hormone

Associated data

  • ClinicalTrials.gov/NCT00866034