Abstract

Objective: Thyroid hormones are essential for fetal growth and neurodevelopment, however, data on cord blood thyroid hormones are sparse in China where maternal age at childbearing is increasing in recent decades. We aimed to assess cord blood levels of free triiodothyronine (FT3), free thyroxine (FT4), and thyroid stimulating hormone (TSH) in full-term Chinese newborns, and examine potential related perinatal factors.Methods: This study included 922 mother-newborn pairs from a prospective birth cohort enrolled in 2012–2013, Shanghai, China. Cord serum concentrations of FT3, FT4, TSH, and TPOAb were measured in newborns.Results: Newborns born via cesarean section had higher cord serum FT3 (mean ± SD: 1.90 ± 1.16 pmol/L) and lower cord serum TSH (5.15 ± 2.60 mIU/L) than those born via vaginal delivery (FT3: 1.62 ± 0.93 pmol/L; TSH: 9.27 ± 6.76 mIU/L). In cesarean section deliveries, the concentration of cord serum FT3 was 0.15 (95%CI: −0.03, 0.33; p = 0.10) pmol/L lower in infants of mothers aged 30–34 years, and 0.57 (95%CI: 0.22, 0.92; p = 0.002) pmol/L lower in infants of mothers ≥35 years compared to infants of mothers <30 years. Large-for-gestational-age (birth weight >90th percentile) was associated with higher TSH (p = 0.02). Similar results were also found in vaginal deliveries.Conclusions: In this Chinese term birth cohort, newborns born via cesarean section had higher cord serum FT3 and lower TSH than those born via vaginal delivery. Advanced maternal age was associated with lower fetal FT3. Further research is needed to understand whether this association may mediate the adverse impact of advanced maternal age on neurodevelopment in early life.

Highlights

  • Thyroid hormones, thyroxine (T4), and triiodothyronine (T3) are essential for fetal growth and neurodevelopment [1]

  • We have presented the data on cord serum levels of FT3, FT4, FT3/FT4 ratio, thyroid stimulating hormone (TSH), and Thyroid peroxidase antibody (TPOAb) in a contemporary Chinese term birth cohort

  • Advanced maternal age has been associated with higher risks of subclinical hypothyroidism [41] and neonatal congenital hypothyroidism (CH) [42] in some studies, but lack of association has been reported in other studies [43, 44]

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Summary

Introduction

Thyroxine (T4), and triiodothyronine (T3) are essential for fetal growth and neurodevelopment [1]. From mid-gestation, fetal hypothalamus-pituitary-thyroid axis becomes gradually functional, and produces increasingly more fetal thyroid hormones including free triiodothyronine (FT3) and free thyroxine (FT4) [2]. Thyroid peroxidase antibody (TPOAb) is Maternal Age and Thyroid Hormones thyroid autoantibody which is not functional antibody and merely reflects autoimmunity [3]. Neonatal TPOAb are mainly from maternal origin [4]. In the context of newborn screening programs for congenital hypothyroidism (CH), thyroid stimulating hormone (TSH) [6, 7], or T4 levels [8, 9] or both have been used [10], while FT3, FT4, and TPOAb levels are not routinely measured

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