Progesterone Suppression of Luteinizing Hormone Pulse Frequency in Adolescent Girls With Hyperandrogenism: Effects of Metformin

J Clin Endocrinol Metab. 2018 Jan 1;103(1):263-270. doi: 10.1210/jc.2017-02068.

Abstract

Context: Polycystic ovary syndrome (PCOS) and adolescent hyperandrogenism (HA) are characterized by rapid luteinizing hormone (LH) pulse frequency. This partly reflects impaired gonadotropin-releasing hormone pulse generator (hypothalamic) sensitivity to progesterone (P4) negative feedback. We assessed whether metformin may improve P4 sensitivity in adolescent HA, for which it is prescribed widely.

Objective: To test the hypothesis that metformin improves hypothalamic P4 sensitivity in adolescent HA.

Design: Nonrandomized, interventional trial.

Setting: Academic clinical research unit.

Participants: Ten adolescent girls with HA.

Intervention: The girls underwent LH sampling every 10 minutes for 11 hours, at study baseline and after 7 days of oral P4 and estradiol (E2). Participants then took metformin (1 g twice daily) for 9.4 to 13.7 weeks, after which participants again underwent frequent LH sampling before and after 7 days of oral P4 and E2 (while continuing metformin). Total and free testosterone (T) and fasting insulin were assessed at each admission. At admissions 1 and 3, 2-hour oral glucose tolerance tests were performed.

Main outcome measure: Metformin-related change in hypothalamic P4 sensitivity index [percent change in LH pulse frequency (before vs after P4 and E2) divided by day 7 P4 level].

Results: Free T levels decreased by 29% with metformin (P = 0.0137). Measures of hyperinsulinemia and P4 sensitivity index did not significantly change with metformin use.

Conclusion: Short-term metformin use improved biochemical hyperandrogenemia, but did not improve hypothalamic sensitivity to P4 suppression, in adolescent girls.

Trial registration: ClinicalTrials.gov NCT01427595.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Adolescent
  • Feedback, Physiological / drug effects*
  • Female
  • Follow-Up Studies
  • Glucose Tolerance Test
  • Humans
  • Hyperandrogenism / drug therapy*
  • Hyperandrogenism / metabolism
  • Hypoglycemic Agents / therapeutic use
  • Insulin Resistance
  • Luteinizing Hormone / metabolism*
  • Metformin / therapeutic use*
  • Progesterone / antagonists & inhibitors*
  • Prognosis
  • Pulsatile Flow / drug effects*

Substances

  • Hypoglycemic Agents
  • Progesterone
  • Luteinizing Hormone
  • Metformin

Associated data

  • ClinicalTrials.gov/NCT01427595