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Fetal thyroid function.
J G Thorpe-Beeston1, K H Nicolaides, A M McGregor
1Department of Obstetrics and Gynaecology, St. Mary's Hospital, London, U.K.
Thyroid : Official Journal of the American Thyroid Association
|January 1, 1992
Summary
Fetal thyroid function matures autonomously in utero. Maternal thyrotropin-releasing hormone (TRH) stimulates fetal thyroid-stimulating hormone (TSH) production, indicating independent pituitary development.
Area of Science:
- Endocrinology
- Fetal Medicine
- Neonatology
Background:
- Cordocentesis enables in utero assessment of fetal thyroid function.
- Fetal thyroid hormone levels and binding globulin concentrations change throughout gestation.
- Maternal thyrotropin-releasing hormone (TRH) can stimulate fetal thyroid-stimulating hormone (TSH) production.
Purpose of the Study:
- To investigate the maturation and regulation of fetal thyroid function during intrauterine life.
- To assess the fetal pituitary-adrenal axis response to exogenous TRH.
- To examine thyroid hormone status in small-for-gestational-age fetuses.
Main Methods:
- Analysis of fetal TSH, thyroxine (TT4, FT4), and triiodothyronine (TT3, FT3) concentrations via cordocentesis.
- Administration of maternal TRH from 25 weeks gestation to evaluate fetal TSH response.
- Comparison of thyroid hormone levels between normal and small-for-gestational-age fetuses.
Main Results:
- Fetal TSH, TBG, TT4, and FT4 increase progressively, reaching adult levels at term or 36 weeks gestation.
- Fetal pituitary-adrenal axis responds robustly and rapidly to maternal TRH, independent of gestational age.
- Small-for-gestational-age fetuses exhibit elevated TSH and reduced TT4/FT4, correlated with hypoxemia and acidemia.
Conclusions:
- Fetal pituitary, thyroid, and liver maturation appear independent and autonomous in utero.
- The fetal pituitary demonstrates heightened sensitivity to TRH compared to adults.
- Altered thyroid hormone levels in compromised fetuses may impact brain development and oxygen requirements.