Longitudinal Evaluation of Fetal and Infant AGD in Healthy Children: Association With Penile Size, Testosterone, and DHT

Author:

Fischer Margit Bistrup12ORCID,Mola Gylli12,Priskorn Lærke12ORCID,Scheel Lone3,Hegaard Hanne Kristine45,Sundberg Karin3ORCID,Frederiksen Hanne12ORCID,Andersson Anna-Maria12,Juul Anders125ORCID,Hagen Casper P12ORCID

Affiliation:

1. Department of Growth and Reproduction, Copenhagen University Hospital—Rigshospitalet , DK-2100 Copenhagen , Denmark

2. International Center for Research and Research Training in Endocrine Disruption of Male Reproduction and Child Health (EDMaRC), Rigshospitalet, University of Copenhagen , DK-2100 Copenhagen , Denmark

3. Center of Fetal Medicine, Department of Obstetrics, Copenhagen University Hospital—Rigshospitalet , DK-2100 Copenhagen , Denmark

4. Department of Obstetrics, The Juliane Marie Centre, Copenhagen University Hospital—Rigshospitalet , DK-2100 Copenhagen , Denmark

5. Department of Clinical Medicine, University of Copenhagen , DK-2200 Copenhagen , Denmark

Abstract

Abstract Context The anogenital distance (AGD) is considered a postnatal readout of early fetal androgen action. Little is known of prenatal AGD and how it correlates with AGD postnatally. Objective We present longitudinal measurements of fetal and infant AGD. We evaluate the impact of testosterone and dihydrotestosterone at minipuberty on AGD and penile size. Methods We performed secondary analyses of an observational, prospective pregnancy and birth cohort, COPANA (2020-2022), at Copenhagen University Hospital—Rigshospitalet, enrolling 685 healthy, singleton pregnant women, of whom 657 attended third trimester ultrasound and 589 infants completed follow-up. Fetal AGD was measured at third semester ultrasound (gestational week 29-34), and infant AGD, penile width, stretched penile length, and circulating testosterone and dihydrotestosterone (LC-MS/MS) were assessed at the minipuberty clinical examination (approximately 3.5 months postpartum): Results AGD was available in 650/657 fetuses (310 boys) and 588/589 infants (287 boys). Boys had longer fetal and infant AGD than girls; fetal AGDas: mean (SD) 21.4 mm (±3.5), fetal AGDaf: 12.8 mm (±2.3), P < .001, infant AGDas: 32.0 mm (±5.6) and infant AGDaf: 15.8 (±3.3), P < .001. Fetal AGD correlated with infant AGD in boys and girls (Spearman r = .275, P < .001 and r = .189, P = .001 respectively), but not with circulating testosterone or dihydrotestosterone at minipuberty. Penile size correlated positively with circulating androgen levels at minipuberty: stretched penile length vs testosterone: r = .235, P < .001. Conclusion AGD is sexually dimorphic already in the third trimester. Fetal and infant AGD correlate. AGD is associated with body size but not circulating androgen levels at minipuberty. These findings suggest that fetal and infant AGD reflect androgen action during early fetal development.

Funder

Rigshospitalets Research Counsil

Læge Sofus Carl Emil Friis og hustru

Aase og Ejnar Danielsens Foundation

Helsefonden

Axel Muusfeldt fond

Danish Centre for Endocrine Disrupting Substances

CeHoS

Publisher

The Endocrine Society

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