Abstract

BackgroundPreterm birth (occurring before 37 completed weeks of gestation) affects 15 million infants annually, 7.5% of which die due to related complications. The detection and early diagnosis are therefore paramount in order to prevent the development of prematurity and its consequences. So far, focus has been laid on the association between reduced intrauterine fetal growth during late gestation and prematurity. The aim of the current study was to investigate the association between accelerated fetal growth in early pregnancy and the risk of preterm birth.MethodsThis prospective cohort study included 69,617 singleton pregnancies without congenital malformations and with available biometric measurements during the first and second trimester. Estimation of fetal growth was based on measurements of biparietal diameter (BPD) at first and second trimester scan. We investigated the association between accelerated fetal growth and preterm birth prior to 37 weeks of gestation. The outcome was further stratified into very preterm birth (before 32 weeks of gestation) or moderate preterm birth (between 32 and 37 weeks of gestation) and medically induced or spontaneous preterm birth and was further explored.ResultsThe odds of prematurity were increased among fetuses with accelerated BPD growth (> 90th centile) estimated between first and second ultrasound scan, even after adjustment for possible confounders (aOR 1.36; 95% CI 1.20–1.54). The findings remained significant what regards moderate preterm births but not very preterm births. Regarding medically induced preterm birth, the odds were found to be elevated in the group of fetuses with accelerated growth in early pregnancy (aOR 1.34; 95% CI 1.11–1.63). On the contrary, fetuses with delayed fetal growth exhibited lower odds for both overall and spontaneous preterm birth.ConclusionsFetuses with accelerated BPD growth in early pregnancy, detected by ultrasound examination during the second trimester, exhibited increased odds of being born preterm. The findings of the current study suggest that fetal growth in early pregnancy should be taken into account when assessing the risk for preterm birth.

Highlights

  • Preterm birth affects 15 million infants annually, 7.5% of which die due to related complications

  • Previous research has described that the etiology and timing of preterm birth is multifactorial and several projects have focused on fetal growth, usually attempting to detect fetuses at increased risk of growth restriction

  • Despite the previous presumption that biological variation in fetal growth is minimal in early pregnancy and that abnormal fetal growth manifests at a later stage, there have been a number of studies showing the impact of fetal growth during early gestation on adverse pregnancy outcomes [8,9,10,11]

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Summary

Introduction

Preterm birth (occurring before 37 completed weeks of gestation) affects 15 million infants annually, 7.5% of which die due to related complications. The aim of the current study was to investigate the association between accelerated fetal growth in early pregnancy and the risk of preterm birth. Only few reports have described the effect of increased fetal size at birth and spontaneous preterm onset of labor; in a population-based, as well as a hospitalbased registry study performed in Sweden and Canada respectively, the authors demonstrated an increased risk for prematurity among fetuses with birthweight exceeding the expected [6, 7]. Lampl et al followed fetal growth in 3927 pregnancies from gestational week 16 up to spontaneous birth and observed an increased risk for prematurity among fetuses with accelerated growth in the second trimester [11]. Pedersen et al investigated fetal growth in 8215 early singleton pregnancies and reported an increased risk of preterm birth among fetuses with accelerated fetal growth, with results almost reaching statistical significance [10]. In order to overcome possible statistical challenges and enhance clinical relevance, we decided to perform a study with serial ultrasound measurements in a large, low risk obstetric population

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