Abstract

Human chorionic gonadotropin (hCG) is a pregnancy-specific hormone that regulates placental development. hCG concentrations vary widely throughout gestation and differ based on fetal sex. Abnormal hCG concentrations are associated with adverse pregnancy outcomes including fetal growth restriction. We studied the association of hCG concentrations with fetal growth and birth weight. In addition, we investigated effect modification by gestational age of hCG measurement and fetal sex. Total serum hCG (median 14.4 weeks, 95 % range 10.1–26.2), estimated fetal weight (measured by ultrasound during 18–25th weeks and >25th weeks) and birth weight were measured in 7987 mother–child pairs from the Generation R cohort and used to establish fetal growth. Small for gestational age (SGA) was defined as a standardized birth weight lower than the 10th percentile of the study population. There was a non-linear association of hCG with birth weight (P = 0.009). However, only low hCG concentrations measured during the late first trimester (11th and 12th week) were associated with birth weight and SGA. Low hCG concentrations measured in the late first trimester were also associated with decreased fetal growth (P = 0.0002). This was the case for both male and female fetuses. In contrast, high hCG concentrations during the late first trimester were associated with increased fetal growth amongst female, but not male fetuses. Low hCG in the late first trimester is associated with lower birth weight due to a decrease in fetal growth. Fetal sex differences exist in the association of hCG concentrations with fetal growth.

Highlights

  • Optimal intrauterine conditions are essential for proper fetal development and growth

  • Our study shows that low Human chorionic gonadotropin (hCG) concentrations in the late first trimester are associated with lower birth weight and an increased risk of Small for gestational age (SGA)

  • We demonstrate that the association of low hCG concentrations in the late first trimester with lower birth weight arises due to a decrease in fetal growth during the second half of pregnancy

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Summary

Introduction

Optimal intrauterine conditions are essential for proper fetal development and growth. A suboptimal intrauterine environment leads to fetal adaptations that may affect fetal growth and thereby lead to lower birth weight [3, 4]. Besides promoting progesterone production by corpus luteal cells, hCG has been shown to regulate many processes that are related to fetal growth including trophoblast differentiation, uterine growth, various aspects of placentation as well as uterine angiogenesis and vasculogenesis [7, 8]. HCG has been shown to stimulate the production of endocrine gland-derived vascular endothelial growth factor (EG-VEGF), which is involved in the physiology of placental development [9, 10]. By acting on cytotrophoblast cells, EG-VEGF is involved in the process of trophoblast shell and arterial plugs formation, necessary for preventing maternal blood flow into the intervillous space during early pregnancy [9]. hCG may directly influence uterine and fetal growth by acting on gonadotropin receptors present in the uterine tissue and fetal membranes [8, 11, 12]

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