Skip to main navigation Skip to search Skip to main content

Myo-inositol Supplementation to Prevent Pregnancy Complications in Polycystic Ovary Syndrome: A Randomized Clinical Trial

  • Anne W.T. van der Wel
  • , Chryselle M.C. Frank
  • , Rebekka Bout-Rebel
  • , Ruben G. Duijnhoven
  • , Bo E. van Bree
  • , Olivier Valkenburg
  • , Salwan Al-Nasiry
  • , Robbert H.F. van Oppenraaij
  • , Tatjana E. Vogelvang
  • , Michelle E.M.H. Westerhuis
  • , Hedwig P. van de Nieuwenhof
  • , Susanne C.J.P. Gielen
  • , Myrthe L. Bandell
  • , Mireille N. Bekker
  • , Maurice G.A.J. Wouters
  • , Velja Mijatovic
  • , Arie Franx
  • , Cornelis B. Lambalk
  • , Frank J.M. Broekmans
  • , Sabina de Weerd
  • Jet M.H. Gerards, Jelle H. Baalman, Jeroen van Disseldorp, Josje Langenveld, Marlise N. Gunning, Geert W.J. Frederix, Rebecca C. Painter, Bart C.J.M. Fauser, Joop S.E. Laven, Bas B. van Rijn
  • Amsterdam UMC
  • University Medical Centre Utrecht
  • Maastricht University
  • Maasstad Hospital
  • Diakonessenhuis Utrecht
  • Catharina Hospital
  • Jeroen Bosch Ziekenhuis
  • Franciscus Gasthuis & Vlietland
  • Albert Schweitzer Ziekenhuis
  • Utrecht University
  • Centre for Reproductive Medicine
  • Medisch Spectrum Twente
  • St. Antonius Ziekenhuis
  • Zuyderland Medical Center (Heerlen)
  • Amsterdam Reproduction and Development Research Institute
  • Maxima Medical Center
  • Eindhoven University of Technology

Research output: Contribution to journalArticleAcademic

7 Citations (Scopus)
56 Downloads (Pure)

Abstract

Importance: 

Pregnant individuals with polycystic ovary syndrome (PCOS) present with a higher risk of pregnancy complications, including gestational diabetes, preeclampsia, and preterm birth. Myo-inositol supplementation may reduce these risks. 

Objective: 

To determine whether daily supplementation with myo-inositol during pregnancy among individuals with PCOS reduces the risk of a composite outcome of gestational diabetes, preeclampsia, and preterm birth. 

Design, Setting, and Participants:

This double-blind, placebo-controlled, randomized trial was conducted at 13 hospitals in the Netherlands. Pregnant individuals with PCOS who were between 8 and 16 weeks' gestation were enrolled between June 2019 and March 2023. Final follow-up was complete on December 27, 2023. Analyses were conducted July 2024. 

Interventions: 

Participants were randomized on a 1:1 basis to receive sachets with either myo-inositol, 2 g, with 0.2 mg of folic acid twice daily (n = 230) or matching placebo with 0.2 mg of folic acid only (n = 234) until delivery. Main Outcomes and Measures: The primary outcome was a composite of gestational diabetes, preeclampsia, or preterm birth (before 37 weeks' gestation). 

Results: 

Among 464 participants, the mean (SD) age was 31.5 (3.8) years; 18 participants (3.9%) reported Asian race and 395 (86.1%) reported White race. The prevalence of biochemical hyperandrogenism was higher at baseline in the myo-inositol group than the placebo group (29.0% [53 of 180] vs 18.5% [37 of 193]). A primary outcome event occurred in 25.0% (n = 56) of participants in the myo-inositol group and 26.8% (n = 61) in the placebo group (relative risk, 0.93 [95% CI, 0.68-1.28]; P = .67). 

Conclusions and Relevance: 

Myo-inositol supplementation during pregnancy did not reduce the incidence of a composite of gestational diabetes, preeclampsia, or preterm birth in patients with PCOS. 

Trial Registration: 

onderzoekmetmensen.nl Identifier: NL67329.078.18.

Original languageEnglish
Pages (from-to)1151-1159
Number of pages9
JournalJAMA
Volume334
Issue number13
Early online date8 Sept 2025
DOIs
Publication statusPublished - 7 Oct 2025

Bibliographical note

Publisher Copyright:
© 2025 American Medical Association.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Fingerprint

Dive into the research topics of 'Myo-inositol Supplementation to Prevent Pregnancy Complications in Polycystic Ovary Syndrome: A Randomized Clinical Trial'. Together they form a unique fingerprint.

Cite this