Affiliation:
1. Department of General Pediatrics, University of Münster , 48149 Münster , Germany
2. Department of Growth and Reproduction, Copenhagen University Hospital—Rigshospitalet , 2100 Copenhagen , Denmark
3. International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen , 2100 Copenhagen , Denmark
4. Department of Clinical Medicine, University of Copenhagen , 2100 Copenhagen , Denmark
Abstract
Abstract
Context
The hypothalamic-pituitary-gonadal axis's transient activity in infancy, i.e, minipuberty, is considered crucial for male reproductive function. Historically, minipuberty has been considered a passive response triggered by the withdrawal of placental steroids at birth. However, given its potential link to adult reproductive function, we hypothesize that minipuberty is a partially genetically regulated process, suggesting a link between the genetic architecture of reproductive hormone concentrations across lifespan.
Objective
To investigate the association of UK Biobank Study-based polygenic scores (PGS) of adult total testosterone (T) and sex hormone-binding globulin (SHBG) concentrations with trajectories of reproductive hormones concentrations in male infants.
Design
Prospective, longitudinal birth cohort (The COPENHAGEN Minipuberty Study, 2016-2018, ClinTrial: NCT02784184). Individual PGSs in male infants derived from published literature were calculated for total T and SHBG. The associations with mean SD scores (SDS) of reproductive hormone concentrations in infancy were tested.
Setting
Population-based.
Patients or other participants
Healthy, male, term, singleton newborns were followed with repeated clinical examinations including blood sampling during a 1-year follow-up (n = 109).
Main outcome measures
Circulating reproductive hormone concentrations.
Results
T-PGSadult were significant associated with mean T-SDSinfancy, mean SHBG-SDSinfancy, and mean LH-SDSinfancy (P = .02, <.001 and .03, with r2 = 0.05, 0.21 and 0.04, respectively). SHBG-PGSadult was significantly associated with mean SHBG-SDSinfancy (P < .001, r2 = 0.18). T-PGSadult explained 5% and 21% of the phenotypic variation in infancy of mean T-SDSinfancy and SHBG-SDSinfancy, respectively.
Conclusion
Our findings suggest that the genetic architecture underlying total T and SHBG in adults also associates with hormone concentrations and their trajectories during infancy.
Funder
Deutsche Forschungsgemeinschaft
International Research and Research Training Centre for Male Reproduction and Child Health
Candy Foundation
Absalon Foundation
the European Union’s Horizon 2020
Danish Environmental Protection Agency
Capital Region of Denmark
Research Council of Rigshospitalet
Aase og Ejnar Danielsens Fond