Andersen Stine Linding, Laurberg Peter
Department of Endocrinology, Aalborg University Hospital; Department of Clinical Biochemistry, Aalborg University Hospital.
Department of Endocrinology, Aalborg University Hospital; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark.
Int J Womens Health. 2016 Sep 19;8:497-504. doi: 10.2147/IJWH.S100987. eCollection 2016.
Hyperthyroidism in women who are of childbearing age is predominantly of autoimmune origin and caused by Graves' disease. The physiological changes in the maternal immune system during a pregnancy may influence the development of this and other autoimmune diseases. Furthermore, pregnancy-associated physiological changes influence the synthesis and metabolism of thyroid hormones and challenge the interpretation of thyroid function tests in pregnancy. Thyroid hormones are crucial regulators of early development and play an important role in the maintenance of a normal pregnancy and in the development of the fetus, particularly the fetal brain. Untreated or inadequately treated hyperthyroidism is associated with pregnancy complications and may even program the fetus to long-term development of disease. Thus, hyperthyroidism in pregnant women should be carefully managed and controlled, and proper management involves different medical specialties. The treatment of choice in pregnancy is antithyroid drugs (ATDs). These drugs are effective in the control of maternal hyperthyroidism, but they all cross the placenta, and so need careful management and control during the second half of pregnancy considering the risk of fetal hyper- or hypothyroidism. An important aspect in the early pregnancy is that the predominant side effect to the use of ATDs in weeks 6-10 of pregnancy is birth defects that may develop after exposure to available types of ATDs and may be severe. This review focuses on four current perspectives in the management of overt hyperthyroidism in pregnancy, including the etiology and incidence of the disease, how the diagnosis is made, the consequences of untreated or inadequately treated disease, and finally how to treat overt hyperthyroidism in pregnancy.
育龄期女性的甲状腺功能亢进主要源于自身免疫,由格雷夫斯病引起。孕期母体免疫系统的生理变化可能会影响这种疾病及其他自身免疫性疾病的发展。此外,与妊娠相关的生理变化会影响甲状腺激素的合成和代谢,对孕期甲状腺功能检查结果的解读提出挑战。甲状腺激素是早期发育的关键调节因子,在维持正常妊娠及胎儿发育,尤其是胎儿大脑发育过程中发挥重要作用。未经治疗或治疗不充分的甲状腺功能亢进与妊娠并发症相关,甚至可能使胎儿易于发生长期疾病。因此,孕妇的甲状腺功能亢进应得到仔细管理和控制,而恰当的管理涉及不同医学专业。孕期的治疗选择是抗甲状腺药物(ATD)。这些药物能有效控制母体甲状腺功能亢进,但它们都会穿过胎盘,因此在妊娠后半期,考虑到胎儿甲状腺功能亢进或减退的风险,需要仔细管理和控制。妊娠早期的一个重要方面是,在妊娠第6至10周使用ATD的主要副作用是出生缺陷,接触现有类型的ATD后可能会出现出生缺陷,且可能很严重。本综述重点关注目前妊娠显性甲状腺功能亢进管理中的四个观点,包括该疾病的病因和发病率、诊断方法、未经治疗或治疗不充分的疾病后果,以及最后如何治疗妊娠显性甲状腺功能亢进。