Thyroid disorders associated with pregnancy: etiology, diagnosis, and management.

John H Lazarus
{"title":"Thyroid disorders associated with pregnancy: etiology, diagnosis, and management.","authors":"John H Lazarus","doi":"10.2165/00024677-200504010-00004","DOIUrl":null,"url":null,"abstract":"<p><p>Pregnancy has an effect on thyroid economy with significant changes in iodine metabolism, serum thyroid binding proteins, and the development of maternal goiter especially in iodine-deficient areas. Pregnancy is also accompanied by immunologic changes, mainly characterized by a shift from a T helper-1 (Th1) lymphocyte to a Th2 lymphocyte state. Thyroid peroxidase antibodies are present in 10% of women at 14 weeks' gestation, and are associated with (i) an increased pregnancy failure (i.e. abortion), (ii) an increased incidence of gestational thyroid dysfunction, and (iii) a predisposition to postpartum thyroiditis. Thyroid function should be measured in women with severe hyperemesis gravidarum but not in every patient with nausea and vomiting during pregnancy. Graves hyperthyroidism during pregnancy is best managed with propylthiouracil administered throughout gestation. Thyroid-stimulating hormone-receptor antibody measurements at 36 weeks' gestation are predictive of transient neonatal hyperthyroidism, and should be checked even in previously treated patients receiving thyroxine. Postpartum exacerbation of hyperthyroidism is common, and should be evaluated in women with Graves disease not on treatment. Radioiodine therapy in pregnancy is absolutely contraindicated. Hypothyroidism (including subclinical hypothyroidism) occurs in about 2.5% of pregnancies, and may lead to obstetric and neonatal complications as well as being a cause of infertility. During the last few decades, evidence has been presented to underpin the critical importance of adequate fetal thyroid hormone levels in order to ensure normal central and peripheral nervous system maturation. In iodine-deficient and iodine-sufficient areas, low maternal circulating thyroxine levels have been associated with a significant decrement in child IQ and development. These data suggest the advisability of further evaluation for a screening program early in pregnancy to identify women with hypothyroxinemia, and the initiation of prompt treatment for its correction. Hypothyroidism in pregnancy is treated with a larger dose of thyroxine than in the nonpregnant state. Postpartum thyroid dysfunction (PPTD) occurs in 50% of women found to have thyroid peroxidase antibodies in early pregnancy. The hypothyroid phase of PPTD is symptomatic and requires thyroxine therapy. A high incidence (25-30%) of permanent hypothyroidism has been noted in these women. Women having transient PPTD with hypothyroidism should be monitored frequently, as there is a 50% chance of these patients developing hypothyroidism during the next 7 years.</p>","PeriodicalId":23310,"journal":{"name":"Treatments in Endocrinology","volume":"4 1","pages":"31-41"},"PeriodicalIF":0.0000,"publicationDate":"2005-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2165/00024677-200504010-00004","citationCount":"63","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Treatments in Endocrinology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2165/00024677-200504010-00004","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 63

Abstract

Pregnancy has an effect on thyroid economy with significant changes in iodine metabolism, serum thyroid binding proteins, and the development of maternal goiter especially in iodine-deficient areas. Pregnancy is also accompanied by immunologic changes, mainly characterized by a shift from a T helper-1 (Th1) lymphocyte to a Th2 lymphocyte state. Thyroid peroxidase antibodies are present in 10% of women at 14 weeks' gestation, and are associated with (i) an increased pregnancy failure (i.e. abortion), (ii) an increased incidence of gestational thyroid dysfunction, and (iii) a predisposition to postpartum thyroiditis. Thyroid function should be measured in women with severe hyperemesis gravidarum but not in every patient with nausea and vomiting during pregnancy. Graves hyperthyroidism during pregnancy is best managed with propylthiouracil administered throughout gestation. Thyroid-stimulating hormone-receptor antibody measurements at 36 weeks' gestation are predictive of transient neonatal hyperthyroidism, and should be checked even in previously treated patients receiving thyroxine. Postpartum exacerbation of hyperthyroidism is common, and should be evaluated in women with Graves disease not on treatment. Radioiodine therapy in pregnancy is absolutely contraindicated. Hypothyroidism (including subclinical hypothyroidism) occurs in about 2.5% of pregnancies, and may lead to obstetric and neonatal complications as well as being a cause of infertility. During the last few decades, evidence has been presented to underpin the critical importance of adequate fetal thyroid hormone levels in order to ensure normal central and peripheral nervous system maturation. In iodine-deficient and iodine-sufficient areas, low maternal circulating thyroxine levels have been associated with a significant decrement in child IQ and development. These data suggest the advisability of further evaluation for a screening program early in pregnancy to identify women with hypothyroxinemia, and the initiation of prompt treatment for its correction. Hypothyroidism in pregnancy is treated with a larger dose of thyroxine than in the nonpregnant state. Postpartum thyroid dysfunction (PPTD) occurs in 50% of women found to have thyroid peroxidase antibodies in early pregnancy. The hypothyroid phase of PPTD is symptomatic and requires thyroxine therapy. A high incidence (25-30%) of permanent hypothyroidism has been noted in these women. Women having transient PPTD with hypothyroidism should be monitored frequently, as there is a 50% chance of these patients developing hypothyroidism during the next 7 years.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
与妊娠相关的甲状腺疾病:病因、诊断和管理。
妊娠对甲状腺经济有影响,碘代谢、血清甲状腺结合蛋白发生显著变化,特别是在缺碘地区,孕妇甲状腺肿大的发生。妊娠还伴有免疫变化,主要表现为T辅助-1 (Th1)淋巴细胞状态向Th2淋巴细胞状态转变。10%的妊娠14周妇女存在甲状腺过氧化物酶抗体,并与(i)妊娠失败(即流产)增加,(ii)妊娠期甲状腺功能障碍发生率增加以及(iii)产后甲状腺炎易感性相关。严重妊娠剧吐的妇女应测量甲状腺功能,但不应测量所有妊娠期恶心和呕吐的患者。妊娠期间Graves甲亢最好在妊娠期间用丙硫脲嘧啶治疗。妊娠36周时促甲状腺激素受体抗体测量可预测新生儿短暂性甲状腺功能亢进,即使在先前接受甲状腺素治疗的患者中也应进行检查。甲状腺机能亢进的产后加重是常见的,应该在Graves病未接受治疗的妇女中进行评估。妊娠期放射性碘治疗是绝对禁忌症。甲状腺功能减退(包括亚临床甲状腺功能减退)发生在约2.5%的孕妇中,可能导致产科和新生儿并发症,也是不孕的原因之一。在过去的几十年里,证据已经提出了支持足够的胎儿甲状腺激素水平的关键重要性,以确保正常的中枢和周围神经系统成熟。在缺碘和足碘地区,母亲循环甲状腺素水平低与儿童智商和发育显著下降有关。这些数据表明,在妊娠早期进一步评估筛查方案以识别甲状腺功能低下的妇女是可取的,并开始及时治疗以纠正其。妊娠期甲状腺功能减退症的治疗剂量比未妊娠期大。产后甲状腺功能障碍(PPTD)发生在50%的妇女发现有甲状腺过氧化物酶抗体在妊娠早期。PPTD的甲状腺功能减退期是有症状的,需要甲状腺素治疗。在这些妇女中,永久性甲状腺功能减退的发生率很高(25-30%)。患有短暂性PPTD并甲状腺功能减退的妇女应经常监测,因为这些患者在未来7年内有50%的机会发展为甲状腺功能减退。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Oxyntomodulin Prenatal treatment of congenital adrenal hyperplasia : do we have enough evidence? The role of melanocyte-stimulating hormone in insulin resistance and type 2 diabetes mellitus. The treatment of severe postmenopausal osteoporosis : a review of current and emerging therapeutic options. Thiazolidinediones : beyond glycemic control.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1