Abstract

BackgroundEvidence from animal studies has indicated that neonatal thyroid function is vital for the reproductive development. Anogenital distance (AGD), a sensitive biomarker of the fetal hormonal milieu, can be used to predict adult reproductive disorders. However, few human studies have examined the association between neonatal thyroid function and AGD. We aimed to explore their associations in a birth cohort study.MethodsConcentrations of thyroid stimulating hormone (TSH) and thyroid hormones (THs), including total triiodothyronine (TT3), total thyroxine (TT4), free triiodothyronine (FT3), and free thyroxine (FT4) were measured in cord plasma in the Shanghai-Minhang Birth Cohort. The offspring AGD (AGDAP [anus–penis] and AGDAS [anus–scrotum] for boys and AGDAC [anus–clitoris] and AGDAF [anus–fourchette] for girls), body weight and anogenital index (AGI = AGD/weight [mm/kg]) were obtained at each follow-up visit. In total, 344 children (194 boys and 150 girls) with cord plasma concentrations of THs and TSH and at least one AGD measurement at birth and at 6, 12, and 48 months of age were included. Multiple linear regression and generalized estimating equation (GEE) models were used to examine the associations of cord plasma concentrations of THs and TSH with AGI.ResultsMultiple linear regression models showed inverse associations of TT4, FT3, and FT4 with female AGI, although statistical significance was only reached at birth, 6 and 48 months of age. These associations were also found in GEE models: higher TT4 and FT4 concentrations were associated with lower AGIAC (TT4: β = -0.27, 95% CI: -0.50, -0.03 for middle vs. lowest tertile; FT4: β = -0.38, 95% CI: -0.61, -0.16 for middle and β = -0.30, 95% CI: -0.55, -0.04 for highest vs. lowest tertile). Besides, girls with the highest tertile of FT3 concentrations had lower AGIAF than those with the lowest tertile (the highest vs. lowest tertile: β = -0.22, 95% CI: -0.36, -0.08). Positive associations between TSH and AGI at birth and at 12 months of age were observed in boys.ConclusionsThis study provides further evidence on the effects of neonatal thyroid function on reproductive development at an early life stage.

Highlights

  • Accumulating evidence from animal studies has indicated that neonatal thyroid function influences gonadal differentiation and reproductive function [1,2,3,4]

  • Only one human study has assessed the associations of thyroid stimulating hormone (TSH), free triiodothyronine (FT3), and free thyroxine (FT4) concentrations in umbilical cord serum with Anogenital distance (AGD) at birth [18], indicating that thyroid function may be involved in male gonadal development in early life stages

  • We examined the longitudinal associations between neonatal thyroid function, as reflected by the concentrations of TSH and thyroid hormones (THs, including total triiodothyronine (TT3), total thyroxine (TT4), FT3, and FT4)) in cord plasma, and repeated AGD measurements from birth to 48 months of age

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Summary

Introduction

Accumulating evidence from animal studies has indicated that neonatal thyroid function influences gonadal differentiation and reproductive function [1,2,3,4]. Measurements of AGD at birth and during early childhood are known to track through adulthood and can be used to predict various reproductive health disorders in adult humans [13, 14]. Only one human study has assessed the associations of thyroid stimulating hormone (TSH), free triiodothyronine (FT3), and free thyroxine (FT4) concentrations in umbilical cord serum with AGD at birth [18], indicating that thyroid function may be involved in male gonadal development in early life stages. Evidence from animal studies has indicated that neonatal thyroid function is vital for the reproductive development. We aimed to explore their associations in a birth cohort study

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