Bumpy and Smoother Pathways of Puberty Hormone Change: A Novel Way to Define Gonadal Hormone Trajectories in Adolescents

Author:

Steinbeck Katharine S12ORCID,Garden Frances L34ORCID,Cheng Hoi Lun12ORCID,Luscombe Georgina M5ORCID,Handelsman David J6ORCID

Affiliation:

1. The University of Sydney, Faculty of Medicine and Health, Sydney Medical School, Discipline of Child and Adolescent Health, Westmead, NSW, Australia

2. The Children’s Hospital at Westmead, Academic Department of Adolescent Medicine, Westmead, NSW, Australia

3. University of New South Wales, South Western Sydney Clinical School, Liverpool, NSW, Australia

4. Ingham Institute for Applied Medical Research, Respiratory Medicine Research Stream, Liverpool, NSW, Australia

5. The University of Sydney, Faculty of Medicine and Health, School of Rural Health, Orange, NSW, Australia

6. The University of Sydney, ANZAC Research Institute, Concord, NSW, Australia

Abstract

Abstract Context The study of gonadal hormone effects on adolescent wellbeing has been limited by logistical challenges. Urine hormone profiling offers new opportunities to understand the health and behavioral implications of puberty hormones. Objective To characterize pubertal change in urinary testosterone and estradiol among male and female adolescents, respectively. Design Three-year prospective cohort study. Setting Australian regional community. Participants 282 (163 male) normally developing adolescents aged 11.8 ± 1.0 years at baseline. Main outcome measure Quarterly urine measurements of testosterone and estradiol (mass spectrometry); annual anthropometric assessment and Tanner stage (TS) self-report. Results Two-class sigmoidal and quadratic growth mixture models (centered on age at TS3) were identified as best-fit for describing testosterone (male) and estradiol (female) change. Classes 1 (male: 63%; female: 82%) and 2 (male: 37%; female: 18%) were respectively named the “stable” and “unstable” trajectories, characterized by different standard deviation of quarterly hormone change and magnitude of hormone peaks and troughs (all P < 0.001). Compared with class 1 (stable), class 2 males were taller at baseline (154 vs 151 cm), reported earlier and faster TS progression (P < 0.01), and showed higher serum testosterone levels at baseline and 3 years (P ≤ 0.01). Class 2 females exhibited smaller height and weight gains over the 3 years and had higher baseline serum estradiol (249 vs 98 pmol/L; P = 0.002) than class 1. Conclusions Adolescents showed 2 distinct urinary gonadal hormone trajectories, characterized by stability of change over time, which were not associated with consistent anthropometric differences. Results provide a methodology for studying gonadal hormone impacts on other aspects of biopsychosocial wellbeing. Identification of potential “at-risk” hormone groups would be important for planning supportive interventions.

Funder

National Health and Medical Research Council of Australia

Thyne Reid Foundation

The Balnaves Foundation

Country Women’s Association of New South Wales and Sydney Medical School

Publisher

The Endocrine Society

Subject

Endocrinology, Diabetes and Metabolism

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