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The association of maternal thyroid function with placental hemodynamics
M Barjaktarovic1,2,3, T I M Korevaar1,2,3, L Chaker2,3
1The Generation R Study Group, Erasmus Medical Center, Rotterdam, The Netherlands.
Human Reproduction (Oxford, England)
|January 29, 2017
Summary
Higher maternal free thyroxine (FT4) in early pregnancy is linked to increased placental vascular resistance. This finding may explain FT4
Area of Science:
- Obstetrics and Gynecology
- Endocrinology
- Perinatology
Background:
- Thyroid hormone (TH) plays a role in placental development, influencing trophoblast proliferation and invasion.
- Suboptimal placental function is linked to adverse pregnancy outcomes like preeclampsia, fetal growth restriction, and preterm delivery.
Purpose of the Study:
- To investigate the clinical association between maternal thyroid function and placental hemodynamic function during pregnancy.
Main Methods:
- Prospective cohort study of 7069 pregnant women (The Generation R cohort).
- Maternal thyroid-stimulating hormone (TSH) and free thyroxine (FT4) levels measured in early pregnancy.
- Placental function assessed via Doppler ultrasound, measuring umbilical and uterine artery resistance indices (PI and RI) and uterine artery notching.
Main Results:
- Higher FT4 concentrations were positively associated with increased umbilical artery PI (second and third trimesters) and uterine artery RI (second trimester).
- Elevated FT4 also correlated with an increased risk of uterine artery notching (third trimester).
- Associations between thyroid function and preeclampsia/birth weight were partially mediated by placental function changes (10.4% and 12.5% respectively).
Conclusions:
- Elevated maternal FT4 in early pregnancy is associated with increased placental vascular resistance in both maternal and fetal compartments.
- These placental changes may contribute to the link between higher FT4 and adverse pregnancy outcomes such as preeclampsia and fetal growth restriction.
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