Evidence map›Paper›PMID 41955216›Full record

ArticleThe Journal of clinical endocrinology and metabolism2026

Steroids, stress, and body mass index interact to accelerate female pubertal development.

Lauren C Houghton, Eva Siegel, Ying Wei, Stefan A Wudy, Michaela F Hartmann, Frank Stanczyk, Julia A Knight, Irene L Andrulis, Angela R Bradbury, Lisa Schwartz and 7 more

Abstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Steroids, stress, and body mass index interact to accelerate female pubertal development.The Journal of clinical endocrinology and metabolism · 2026
    Article
  2. Review
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

17 authors.

Lauren C HoughtonDepartment of Epidemiology, Columbia University Mailman School of Public Health, NewYork, NY 10032, USA.ORCID 0000-0002-1432-1580
Eva SiegelDepartment of Epidemiology, Columbia University Mailman School of Public Health, NewYork, NY 10032, USA.
Ying WeiDepartment of Biostatistics, Columbia University Mailman School of Public Health, NewYork, NY 10032, USA.
Stefan A WudySteroid Research and Mass Spectrometry Unit, Laboratory of Translational Hormone Analytics, Division of Pediatric Endocrinology and Diabetology, Center of Child and Adolescent Medicine, Justus Liebig University, Giessen 35392, Germany.
Michaela F HartmannSteroid Research and Mass Spectrometry Unit, Laboratory of Translational Hormone Analytics, Division of Pediatric Endocrinology and Diabetology, Center of Child and Adolescent Medicine, Justus Liebig University, Giessen 35392, Germany.
Frank StanczykDepartment of Obstetrics and Gynecology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Julia A KnightSinai Health, Lunenfeld-Tanenbaum Research Institute, Toronto, ON M5G 1X5, Canada.
Irene L AndrulisSinai Health, Lunenfeld-Tanenbaum Research Institute, Toronto, ON M5G 1X5, Canada.
Angela R BradburyMedical Ethics and Health Policy, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Lisa SchwartzThe Children's Hospital of Philadelphia, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
Saundra S BuysDepartment of Medicine, University of Utah Health Sciences Center, Huntsman Cancer Institute, Salt Lake City, UT 84112, USA.
Mary B DalyDepartment of Clinical Genetics, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Esther M JohnDepartments of Epidemiology and Population Health and of Medicine (Oncology) and Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.
Wendy K ChungHerbert Irving Comprehensive Cancer Center, Columbia University Medical Center, NewYork, NY 10032, USA.
Regina M SantellaDepartment of Environmental Health Sciences, Columbia University Mailman School of Public Health, NewYork, NY 10032, USA.
Russell D RomeoDepartment of Neuroscience and Behavior, Barnard College of Columbia University, NewYork, NY 10027, USA.
Mary Beth TerryDepartment of Epidemiology, Columbia University Mailman School of Public Health, NewYork, NY 10032, USA.

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
True Metal fac coreP30ES009089 · NIEHS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Steven N. Chillrud · 1998 to 2026
$44.7M
LEGACY: A Cohort of Youth in Families from the Breast Cancer Family RegistryR01CA138638 · NCI · CANCER PREVENTION INSTIT OF CALIFORNIA · PI JOHN, ESTHER M. · 2011 to 2015
$3.6M
LEGACY: A Cohort of Youth in Families from the Breast Cancer Family RegistryR01CA138819 · NCI · RESEARCH INST OF FOX CHASE CAN CTR · PI BRADBURY, ANGELA R., DALY, MARY BERYL · 2011 to 2015
$3.3M
LEGACY: A cohort of youth in families from the Breast Cancer Family RegistryR01CA138844 · NCI · SINAI HEALTH SYSTEM · PI ANDRULIS, IRENE · 2011 to 2015
$1.8M
Breast Cancer Research FoundationColumbia University P30CA013696Columbia University P30ES009089NCI NIH HHS 5K07CA21816603NCI NIH HHS 5R01CA138638NCI NIH HHS 5R01CA138819NCI NIH HHS 5R01CA138844NCI NIH HHS 5R01CA15986804NCI NIH HHS P30 CA013696NCI NIH HHS R01 CA138638NCI NIH HHS R01 CA138819NCI NIH HHS R01 CA138844NIEHS NIH HHS P30 ES009089
6 · The paper itself

Abstract

contextEstrogens underlie puberty in girls, but the steroid metabolome may also regulate pubertal timing in response to elevated stress and increasing body mass index (BMI).

objectiveOur objective was to identify steroid metabolome patterns linked to accelerated puberty and test whether BMI and stress markers modify this relationship.

methodsFrom the LEGACY Girls Study, a longitudinal cohort followed for 6 years, we selected 327 girls aged 5 to 13 years at baseline to measure 36 steroid metabolites of glucocorticoids, androgens, progesterone, and estrogens in 2 urine samples collected before and during puberty. Parents reported the age at onset of breast development (thelarche), which had a high correlation in the subset with clinically assessed Tanner. Study staff measured height and weight and administered questionnaires, including the Internalizing Composite Scale, a parental proxy of child stress. We estimated hazard ratios (HRs) for the association between doubled steroid metabolites and ages at thelarche, pubarche, and menarche using Weibull survival models, testing interactions with stress and BMI z-scores.

resultsAccelerated thelarche was associated with higher prepubertal urinary metabolites of glucocorticoids (HR = 1.9, 95% CI: 1.5-2.5), androgens (HR = 3.9, 95% CI: 2.7-5.6), and progesterone (HR = 6.7, 95% CI: 4.1-10.9). Girls with high glucocorticoid metabolites combined with high BMI and stress reached thelarche 7 months earlier than their counterparts with low measures in these parameters.

conclusionElevated metabolites of glucocorticoids, androgens, and progesterone are associated with accelerated pubertal onset, and BMI and stress modify this association. Previous studies have focused on estrogens, menarche, and BMI; our results suggest that androgens and stress impact the timing of thelarche as well, explaining secular declines in pubertal timing.

Indexed as

Body Mass IndexPubertySteroidsStress, PsychologicalAdolescentAndrogensChildChild, PreschoolEstrogensFemaleGlucocorticoidsHumansLongitudinal StudiesMenarcheProgesteroneSexual MaturationAndrogensEstrogensGlucocorticoidsProgesteroneSteroidsBMIbreast cancerpubertysteroidstress

Identifiers

PMID41955216
PMCPMC13466949

What OpenQuestion holds

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Registered trials

None linked

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.