Evidence map›Paper›PMID 32776198›Full record

ArticleJournal of endocrinological investigation2021

Sex-dependent associations of maternal androgen levels with offspring BMI and weight trajectory from birth to early childhood.

G Huang, S A Aroner, C P Bay, S E Gilman, A Ghassabian, E B Loucks, S L Buka, R J Handa, B L Lasley, S Bhasin and 1 more

Open access · greenAbstract read
In one paragraph

Article in Journal of endocrinological investigation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.9field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 21 citations in OpenAlex.

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  5. Testosterone mediates life-history trade-offs in female mammals.Biological reviews of the Cambridge Philosophical Society · 2025
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 8 institutions in 1 country.

G HuangSection of Men's Health, Aging and Metabolism, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA. ghuang7@bwh.harvard.edu.
S A AronerDepartment of Psychiatry, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
C P BayCenter for Clinical Investigation, Brigham and Women's Hospital, Boston, MA, USA.
S E GilmanSocial and Behavioral Sciences Branch, Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institute of Health, Bethesda, MD, USA.
A GhassabianDepartments of Pediatrics, Environmental Medicine, and Population Health, New York University School of Medicine, New York, NY, USA.
E B LoucksDepartment of Epidemiology, Brown University School of Public Health, Providence, RI, USA.
S L BukaDepartment of Epidemiology, Brown University School of Public Health, Providence, RI, USA.
R J HandaDepartment of Biomedical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO, USA.
B L LasleyDepartment of Population Health and Reproduction, School of Veterinary Medicine, University of California Davis, Davis, CA, USA.
S BhasinSection of Men's Health, Aging and Metabolism, Department of Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
J M GoldsteinDepartment of Psychiatry, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA.
Brigham and Women's Hospital · USBrown University · USHarvard University · USColorado State University · USEunice Kennedy Shriver National Institute of Child Health and Human Development · USMassachusetts General Hospital · USNew York University · USUniversity of California, Davis · US

Funding

Social determinants of child development and mental healthZIAHD008976 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI GILMAN, STEPHEN · 2018 to 2025
$14.3M
Sex Differences in Major Depression, Part II: Impact of Prenatal Immune, Autonomic and Neurovascular FunctionU54MH118919 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI JILL M GOLDSTEIN · 2020 to 2026
$12.7M
Fetal Antecedents to Depression and Risk for CVDR01MH074679 · NIMH · BRIGHAM AND WOMEN'S HOSPITAL · PI GOLDSTEIN, JILL M · 2007 to 2011
$3.7M
Pathways Linking Education/Health in Middle AdulthoodR01AG023397 · NIA · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI BUKA, STEPHEN L · 2003 to 2006
$2.0M
The New England Family Study: Fifty Year Post-Perinatal Follow-Up for Life CourseRC2AG036666 · NIA · BROWN UNIVERSITY · PI BUKA, STEPHEN L, EATON, CHARLES B · 2009 to 2010
$1.7M
Prenatal Androgens and Cardiometabolic Risk in AdulthoodK08HL132122 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI HUANG, GRACE · 2017 to 2020
$516k
Arizona Biomedical Research Commission ADHS14-00003606NHLBI NIH HHS K08 HL132122NHLBI NIH HHS K08 HL132122-02NIA NIH HHS R01 AG023397NIA NIH HHS R01AG023397NIA NIH HHS RC2 AG036666NIA NIH HHS RC2AG036666NIMH NIH HHS R01 MH074679NIMH NIH HHS R01MH074679NIMH NIH HHS U54 MH118919
6 · The paper itself

Abstract

contextIn preclinical studies, high androgen levels during pregnancy are associated with low birth weight and rapid postnatal weight gain in the offspring. However, human data linking prenatal androgens with birth weight and early life weight gain in the offspring are scarce.

designWe evaluated 516 mother-child pairs enrolled in the New England birth cohorts of the Collaborative Perinatal Project (1959-1966). We assayed androgen bioactivity in maternal sera during third-trimester using a receptor-mediated luciferase expression bioassay. Age and sex-specific BMI Z-scores (BMIz), defined using established standards, were assessed at birth, 4 months, 1 year, 4 years, and 7 years. We used linear mixed models to evaluate the relation of maternal androgens with childhood BMIz overall and by sex. We examined the association of maternal androgens with fetal growth restriction. The association of weight trajectories with maternal androgens was examined using multinomial logistic regression.

resultsHigher maternal androgen levels associated with lower BMIz at birth (β = - 0.39, 95% CI: - 0.73, - 0.06); this relation was sex-dependent, such that maternal androgens significantly associated with BMIz at birth in girls alone (β = - 0.72, 95% CI: - 1.40, - 0.04). The relation of maternal androgens with fetal growth restriction revealed dose threshold effects that differed by sex. There was no significant association between maternal androgens and weight trajectory overall. However, we found a significant sex interaction (p = 0.01); higher maternal androgen levels associated with accelerated catch-up growth in boys (aOR = 2.14, 95% CI: 1.14, 4.03).

conclusionOur findings provide evidence that maternal androgens may have differential effects on the programming of intrauterine growth and postnatal weight gain depending on fetal sex.

Indexed as

Body-Weight TrajectoryPrenatal CareAdultAndrogensBirth WeightBody Mass IndexChildChild DevelopmentChild, PreschoolCohort StudiesCorrelation of DataFemaleHumansInfant, NewbornMaleNew EnglandAndrogensAndrogensBody mass indexChildhoodPrenatalSexWeight growth trajectory

Identifiers

PMID32776198
PMCPMC7873156
OpenAlexW3047983156

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.