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Endocrine Abstracts (2025) 110 EP1082 | DOI: 10.1530/endoabs.110.EP1082

ECEESPE2025 ePoster Presentations Pituitary, Neuroendocrinology and Puberty (220 abstracts)

Longitudinally assessed sex-typed play behaviour and its association with androgen levels during minipuberty in full-term and preterm children

Johanna Eronen 1 , Ulla Sankilampi 1 & Tanja Kuiri-Hänninen 1


1University of Eastern Finland, Kuopio, Finland


JOINT1344

Context: Higher androgen levels during minipuberty have been associated with more masculine sex-typed play behaviour in full-term (FT) infants. On the other hand, reduced sex-typed play behaviour has been reported in preterm (PT) children at the age of five years.

Aim: To investigate the longitudinal development of sex-typed play behaviour and its association with testosterone and DHEAS levels during minipuberty in FT and PT children.

Methods: A standardized psychometric questionnaire Preschool Activities Inventory (PSAI) was used to measure the sex-typed play behaviour in 54 FT (boys n = 26) and 91 PT (boys n = 44) children at three time points: infancy (mean age (SD) 1.2 (0.1), n = 117), early childhood (EC, 3.1 (0.3), n = 89) and late childhood (LC, 9.1 (0.7) n = 63). Higher PSAI score indicates more masculine and lower score more feminine behaviour. Urinary testosterone and DHEAS levels during minipuberty were measured using HPLC-MS/MS. Spearman’s correlation and mixed model were used for statistical analyses.

Results: Both testosterone and DHEAS levels in minipuberty were significantly (P <0.001) higher in PT than in FT infants. DHEAS levels did not differ between sexes, but testosterone levels were higher in boys than in girls (P <0.001). Notably, testosterone levels in PT girls were at the same level as in FT boys. In all the children, testosterone level correlated positively with PSAI in infancy (Spearman’s rho 0.230, P = 0.013) and in EC (rho 0.339, P = 0.001), but not in LC (rho 0.194, P = 0.132). However, no significant associations were observed in the subgroups. In PT boys, DHEAS correlated negatively with PSAI in infancy (P = 0.036), but in the other multivariate analyses including the number of brothers and sisters and the age, neither testosterone nor DHEAS levels were associated with PSAI scores.

Table 1.
InfancyEarly childhood (EC)Late childhood (LC)
BoysFTPTFTPTFTPT
PSAI62.2 (4.4)59.8 (7.8)63.5 (8.7)61.9 (7.4)66.3 (7.0)68.1(7.4)
Change from infancy to ECnot significant (NS)NS
Change from EC to LCNS P <0.001
GirlsFTPTFTPTFTPT
PSAI44.1 (7.5)44.7 (9.2)33.6 (8.9)32.0 (9.2)34.1 (9.3)39.2 (8.7)
Change from infancy to EC P <0.001 P <0.001
Change from EC to LCNS P = 0.002

Conclusions: Prematurity seems to affect the longitudinal development of the PSAI score, but the differences are small. Urinary T or DHEAS measured during minipuberty were not associated with PSAI score after early childhood.

Volume 110

Joint Congress of the European Society for Paediatric Endocrinology (ESPE) and the European Society of Endocrinology (ESE) 2025: Connecting Endocrinology Across the Life Course

European Society of Endocrinology 
European Society for Paediatric Endocrinology 

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