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Aspirin, Birthweight, and Large‐For‐Gestational‐Age Neonates: A Secondary Analysis of the ASPRE Trial

  • Daniel L. Rolnik
  • , Liona C. Poon
  • , Argyro Syngelaki
  • , David Wright
  • , Neil O'Gorman
  • , Catalina de Paco Matallana
  • , Ranjit Akolekar
  • , Deepa Janga
  • , Mandeep Singh
  • , Francisca S. Molina
  • , Nicola Persico
  • , Jacques C. Jani
  • , Walter Plasencia
  • , George Papaioannou
  • , Kinneret Tenenbaum‐Gavish
  • , Hamutal Meiri
  • , Kypros H. Nicolaides
    • Department of Obstetrics and Gynaecology Monash University Clayton Victoria Australia
    • Department of Obstetrics and Gynaecology The Chinese University of Hong Kong Hong Kong Hong Kong
    • Fetal Medicine Research Institute King's College Hospital London UK
    • Institute of Health Research University of Exeter Exeter UK
    • Infants University Hospital Dublin Ireland
    • Hospital Clínico Universitario Virgen de la Arrixaca Murcia Spain
    • Medway Fetal and Maternal Medicine Centre Medway Maritime Hospital Gillingham Kent UK
    • North Middlesex University Hospital NHS Trust London UK
    • Kypros Nicolaides Fetal Medicine and Therapy Centre Burjeel Medical City Abu Dhabi UAE
    • Hospital Universitario Clínico San Cecilio Granada Spain
    • Fondazione IRCCS ca' Granda Ospedale Maggiore Policlinico and University of Milan Milan Italy
    • University Hospital Brugmann Université Libre de Bruxelles Brussels Belgium
    • Fetal Medicine Unit Hospiten Group Santa Cruz de Tenerife Spain
    • Attikon Hospital University of Athens Athens Greece
    • Rabin Medical Center Petah Tikva Israel
    • HyLabs Diagnostics Rehovot Israel

    Research output: Contribution to journalArticlepeer-review

    1 Citation (Scopus)

    Abstract

    ABSTRACTObjectiveTo investigate the effects of aspirin on the distribution of birthweight and its impact on the rates of large‐for‐gestational‐age (LGA) neonates.DesignSecondary analysis of the Combined Multimarker Screening and Randomised Patient Treatment with Aspirin for Evidence‐based Preeclampsia Prevention (ASPRE) trial.SettingThirteen hospitals in England, Spain, Belgium, Greece, Italy and Israel.PopulationParticipants of the ASPRE trial at increased risk of preterm pre‐eclampsia (PE) who had a live birth.MethodsWe compared the birthweight distributions and the rates of LGA neonates between the trial groups. Analyses were stratified according to the presence of pre‐existing diabetes mellitus and the development of PE, and logistic regression was used to investigate independent predictors of LGA neonates with birthweight above the 90th percentile.Main Outcome MeasuresBirthweight distribution and rates of LGA neonates.ResultsAmong 1571 singleton, live neonates (777 from the aspirin group and 794 from the placebo group), aspirin was associated with a shift in birthweight from < 2500 to 2500–4000 g, and birthweight percentile from < 25th to 25th—75th percentiles, with no significant increase in LGA neonates (5.5% vs. 6.2%, p = 0.667). Logistic regression demonstrated a significant interaction between treatment and pre‐existing diabetes (p‐value 0.034), and a positive association between maternal weight and LGA neonates (adjusted odds ratio 1.040, 95% confidence interval 1.030–1.051, p < 0.001).ConclusionsAspirin use is associated with increased birthweight without increasing the rate of LGA neonates. Among women with pre‐existing diabetes, aspirin may be associated with a higher rate of LGA neonates, warranting further investigation.
    Original languageEnglish
    Pages (from-to)1606-1614
    Number of pages9
    JournalBJOG: An International Journal of Obstetrics and Gynaecology
    Volume132
    Issue number11
    DOIs
    Publication statusPublished - 1 Jul 2025

    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

    Keywords

    • Aspirin
    • ASPRE trial
    • birthweight
    • First trimester
    • Large-for-gestational-age
    • LGA
    • Marcosomia
    • Pre-eclampsia
    • Pre-existing diabetes
    • Prevention

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