Review of European Thyroid Association Guideline (2018) for the Manage-ment of Graves’ Hyperthyroidism

F. Fadeev
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引用次数: 5

Abstract

Graves’ disease (GD) is a systemic autoimmune disorder characterized by the infiltration of thyroid antigen-specific T-cells into thyroid-stimulating hormone receptor (TSH-R)-expressing tissues. Stimulatory autoantibodies (Ab) in GD activate the TSH-R leading to thyroid hyperplasia and unregulated thyroid hormone production and secretion. Diagnosis of GD is straightfor-ward in a patient with biochemically confirmed thyrotoxicosis, positive TSH-R-Ab, a hypervascular and hypoechoic thyroid gland (ultrasound), and associated orbitopathy. In GD, measurement of TSH-R-Ab is recommended for an accurate diagno-sis/differential diagnosis, prior to stopping antithyroid drug (ATD) treatment and during pregnancy. Graves’ hyperthyroidism is treated by decreasing thyroid hormone synthesis with the use of ATD, or by reducing the amount of thyroid tissue with radioactive iodine (RAI) treatment or total thyroidectomy. Patients with newly diagnosed Graves’ hyperthyroidism are usually medically treated for 12–18 months with methimazole (MMI) as the preferred drug. In children with GD, a 24- to 36-month course of MMI is recommended. Patients with persistently high TSH-R-Ab at 12–18 months can continue MMI treatment, repeating the TSH-R-Ab measurement after an additional 12 months, or opt for therapy with RAI or thyroidectomy. Women treated with MMI should be switched to propylthiouracil when planning pregnancy and during the first trimester of pregnancy. If a patient relapses after completing a course of ATD, definitive treatment is recommended; however, continued long-term low-dose MMI can be considered. Thyroidectomy should be performed by an experienced high-volume thyroid surgeon. RAI is contraindicated in Graves’ patients with active/severe orbitopathy, and steroid prophylaxis is warranted in Graves’ patients with mild/active orbitopathy receiving RAI. The literature review presented in this article does not claim to be a full-fledged systematic review, not only for the reason that to date, only 51 works have been found at the time of writing in the databases for the keywords «thyroid and COVID-19» and «adrenal and COVID-19», after excluding duplicates, but also because these messages themselves contain little information and are mainly based on analogies with previously existing viral infections and their role in the development of hypothalamus-pituitary axis pathology-adrenal glands and hypothalamus-pituitary-thyroid.
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欧洲甲状腺协会指南(2018)格雷夫斯甲状腺功能亢进管理的回顾
Graves病(GD)是一种以甲状腺抗原特异性t细胞浸润到促甲状腺激素受体(TSH-R)表达组织为特征的系统性自身免疫性疾病。GD中的刺激性自身抗体(Ab)激活TSH-R,导致甲状腺增生和甲状腺激素的产生和分泌不调节。在生化确诊甲状腺毒症、TSH-R-Ab阳性、甲状腺血管增生和低回声(超声)以及相关眼窝病的患者中,GD的诊断是直接的。在GD中,建议在停止抗甲状腺药物(ATD)治疗之前和怀孕期间测量TSH-R-Ab以进行准确诊断/鉴别诊断。Graves甲状腺机能亢进的治疗方法是使用ATD减少甲状腺激素的合成,或使用放射性碘(RAI)治疗或全甲状腺切除术减少甲状腺组织的数量。新诊断的Graves甲亢患者通常以甲巯咪唑(MMI)为首选药物治疗12-18个月。对于患有GD的儿童,建议24至36个月的MMI疗程。在12 - 18个月持续高TSH-R-Ab的患者可以继续MMI治疗,在额外的12个月后重复TSH-R-Ab测量,或选择RAI或甲状腺切除术治疗。接受MMI治疗的妇女在计划妊娠和妊娠早期应改用丙硫脲嘧啶。如果患者在完成一个ATD疗程后复发,建议进行最终治疗;然而,可以考虑长期持续低剂量MMI。甲状腺切除术应由经验丰富的高容量甲状腺外科医生进行。Graves的有动性/重度眼病患者禁行RAI,而Graves的轻度/有动性眼病患者接受RAI时,类固醇预防是有必要的。本文中提出的文献综述并不是一项完整的系统综述,不仅是因为到目前为止,在排除重复后,在数据库中仅发现了51篇关键词为“甲状腺和COVID-19”和“肾上腺和COVID-19”的文献综述。但也因为这些信息本身包含的信息很少,主要是基于与先前存在的病毒感染的类比,以及它们在下丘脑-垂体轴病理-肾上腺和下丘脑-垂体-甲状腺的发展中的作用。
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