人胎儿甲状腺功能。

Endocrine development Pub Date : 2014-01-01 Epub Date: 2014-08-29 DOI:10.1159/000363152
Michel Polak
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引用次数: 38

摘要

甲状腺发育的早期步骤导致其在人类胎儿中的功能,随后进一步成熟,允许人类胎儿分泌大量甲状腺素(T4),在这里进行综述。我们强调T4从孕妇转移到胎儿的重要性,这有助于在怀孕的各个阶段胎儿甲状腺功能和发育。在怀孕的前三个月,甲状腺激素合成与卵泡发生的时间和结构相关性支持了结构和功能成熟密切相关的概念。人甲状腺终末分化遵循精确定时的基因表达程序。钠/碘同调体在人类胎儿甲状腺功能发病中的关键作用。胎儿T4在妊娠第11周检测到,并在整个过程中逐渐增加。在妊娠过程中,甲状腺激素和促甲状腺激素水平的模式是由胎儿血液采样数据给出的,并讨论了在人类胎儿中控制这种成熟的机制。最后,一个原发性人类胎儿甲状腺功能障碍的例子,如在唐氏综合症,给出。对人类胎儿甲状腺功能的生理认识是甲状腺学胎儿医学的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human fetal thyroid function.

The early steps of thyroid development that lead to its function in the human fetus and subsequently the further maturation that allows the human fetus to secrete thyroxine (T4) in a significant amount are reviewed here. We underline the importance of the transfer of T4 from the pregnant woman to her fetus, which contributes at all stages of the pregnancy to fetal thyroid function and development. In the first trimester of pregnancy, the temporal and structural correlation of thyroid hormone synthesis with folliculogenesis supported the concept that structural and functional maturations are closely related. Human thyroid terminal differentiation follows a precisely timed gene expression program. The crucial role of the sodium/iodine symporter for the onset of thyroid function in the human fetus is shown. Fetal T4 is detected by the eleventh week of gestation and progressively increases throughout. The pattern of thyroid hormones and thyroid-stimulating hormone levels in the course of pregnancy is given from fetal blood sampling data, and the mechanisms governing this maturation in the human fetus are discussed. Finally an example of primary human fetal thyroid dysfunction, such as in Down syndrome, is given. The understanding of the physiology of the human fetal thyroid function is the basis for fetal medicine in the field of thyroidology.

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