Abstract

ObjectiveIt is unknown if foetal gender influences maternal thyroid function during pregnancy. We therefore investigated the prevalence of thyroid disorders and determined first-trimester TSH reference ranges according to gender.MethodsA cross-sectional study involving 1663 women with an ongoing pregnancy was conducted. Twin and assisted pregnancies and l-thyroxine or antithyroid treatment before pregnancy were exclusion criteria. Serum TSH, free T4 (FT4) and thyroid peroxidase antibodies (TPOAb) were measured at median (interquartile range; IQR) 13 (11–17) weeks of gestation. Subclinical hypothyroidism (SCH) was present when serum TSH levels were >3.74 mIU/L with normal FT4 levels (10.29–18.02 pmol/L), and thyroid autoimmunity (TAI) was present when TPOAb were ≥60 kIU/L.ResultsEight hundred and forty-seven women were pregnant with a female foetus (FF) and 816 with a male foetus (MF). In women without TAI and during the gestational age period between 9 and 13 weeks (with presumed high-serum hCG levels), median (IQR range) serum TSH in the FF group was lower than that in the MF group: 1.13 (0.72–1.74) vs 1.24 (0.71–1.98) mIU/L; P = 0.021. First-trimester gender-specific TSH reference range was 0.03–3.53 mIU/L in the FF group and 0.03–3.89 mIU/L in the MF group. The prevalence of SCH and TAI was comparable between the FF and MF group: 4.4% vs 5.4%; P = 0.345 and 4.9% vs 7.5%; P = 0.079, respectively.ConclusionsWomen pregnant with an MF have slightly but significantly higher TSH levels and a higher upper limit of the first-trimester TSH reference range, compared with pregnancies with a FF. We hypothesise that this difference may be related to higher hCG levels in women pregnant with a FF, although we were unable to measure hCG in this study. Further studies are required to investigate if this difference has any clinical relevance.

Highlights

  • Thyroid dysfunction in pregnant women is mainly caused by the presence of thyroid autoimmunity (TAI), reflected by increased thyroperoxidase (TPO) and/or thyroglobulin (Tg) antibody levels [1, 2]

  • We report here a cross-sectional analysis of women with ongoing pregnancies that was nested within the ongoing prospective collection of women’s obstetrical parameters and biological data

  • After the exclusion of pregnancies resulting from assisted reproduction (n = 32), multiple pregnancies (n = 48) and women treated with l-thyroxine or antithyroid drugs before screening (n = 39), 1663 women were included for comparison of the prevalence of thyroid disorders and baseline/obstetric characteristics between women pregnant with an female foetus (FF) (n = 847) or a male foetus (MF) (n = 816)

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Summary

Introduction

Thyroid dysfunction in pregnant women is mainly caused by the presence of thyroid autoimmunity (TAI), reflected by increased thyroperoxidase (TPO) and/or thyroglobulin (Tg) antibody levels [1, 2]. In a number of studies, the impact of some thyroid parameters on pregnancy outcomes was different according to the foetal gender [7, 8, 9]. Among euthyroid women with TAI, after adjustment for confounders, only women pregnant with a female foetus (FF) had an increased risk of preterm births [9]. Differences in these pregnancy outcomes according to the foetal gender could be explained in part by a sexspecific maternal–placental–foetal interaction such as higher serum hCG levels in women expecting a FF [10, 11]

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