Hypothyroidism

Peter N Taylor, Marco M Medici, Alicja Hubalewska-Dydejczyk, Kristien Boelaert
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Abstract

Hypothyroidism, the deficiency of thyroid hormone, is a common condition worldwide. It affects almost all body systems and has a wide variety of clinical presentations from being asymptomatic to, in rare cases, life threatening. The classic symptoms of hypothyroidism include fatigue, lethargy, weight gain, and cold intolerance; however, these symptoms are non-specific and the diagnosis is typically made on biochemical grounds through serum thyroid function tests. The most common cause of hypothyroidism is chronic autoimmune thyroiditis (Hashimoto's thyroiditis), although other causes, including drugs (such as amiodarone, lithium, and immune checkpoint inhibitors), radioactive-iodine treatment, and thyroid surgery, are frequent. Historically, severe iodine deficiency was the most common cause. Reference ranges for thyroid function tests are based on fixed percentiles of the population distribution, but there is increasing awareness of the need for more individualised reference intervals based on key factors such as age, sex, and special circumstances such as pregnancy. Levothyroxine monotherapy is the standard treatment for hypothyroidism; it is safe and inexpensive, restores thyroid function tests to within the reference range, and improves symptoms in the majority of patients. However, 10% of patients have persistent symptoms of ill health despite normalisation of thyroid function tests biochemically and a substantial proportion of patients on levothyroxine have thyroid-stimulating hormone concentrations outside the reference range. Ongoing symptoms despite levothyroxine treatment has led to some patients using liothyronine or desiccated thyroid extract. Taken together, these factors have led to intense debate around the treatment thresholds and treatment strategies for hypothyroidism. In this Seminar, we review the epidemiology, genetic determinants, causes, and presentation of hypothyroidism; highlight key considerations and controversies in its diagnosis and management; and provide future directions for research.
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甲状腺功能减退症
甲状腺功能减退症(甲状腺激素缺乏症)是一种全球常见疾病。它影响几乎所有的身体系统,临床表现多种多样,从无症状到极少数情况下危及生命。甲状腺功能减退症的典型症状包括疲劳、嗜睡、体重增加和不耐寒;然而,这些症状都是非特异性的,诊断通常是通过血清甲状腺功能检测的生化指标做出的。甲状腺功能减退症最常见的病因是慢性自身免疫性甲状腺炎(桥本氏甲状腺炎),但其他病因,包括药物(如胺碘酮、锂和免疫检查点抑制剂)、放射性碘治疗和甲状腺手术也很常见。从历史上看,严重缺碘是最常见的原因。甲状腺功能检测的参考范围基于人群分布的固定百分位数,但人们越来越意识到,需要根据年龄、性别和妊娠等特殊情况等关键因素制定更加个性化的参考区间。左甲状腺素单药治疗是甲状腺功能减退症的标准治疗方法;它安全、便宜,能使甲状腺功能检测结果恢复到参考范围内,并能改善大多数患者的症状。然而,尽管甲状腺功能检测的生化指标趋于正常,但仍有10%的患者会持续出现不适症状,而且相当一部分服用左甲状腺素的患者促甲状腺激素浓度超出了参考范围。尽管接受了左甲状腺素治疗,但症状依然存在,这导致一些患者开始使用利甲腺宁或干燥甲状腺提取物。综合这些因素,人们围绕甲减的治疗阈值和治疗策略展开了激烈的讨论。在本次研讨会上,我们回顾了甲状腺功能减退症的流行病学、遗传决定因素、病因和表现;强调了其诊断和管理中的主要注意事项和争议;并提供了未来的研究方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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