Kibirige Davis, Luzinda Kenneth, Ssekitoleko Richard
Department of Medicine, Uganda Martyrs Hospital Lubaga, Kampala, Uganda.
Thyroid Res. 2013 Feb 7;6(1):3. doi: 10.1186/1756-6614-6-3.
Lithium is an integral drug used in the management of acute mania, unipolar and bipolar depression and prophylaxis of bipolar disorders. Thyroid abnormalities associated with treatment with lithium have been widely reported in medical literature to date. These include goitre, hypothyroidism, hyperthyroidism and autoimmune thyroiditis. This current review explores the varied thyroid abnormalities frequently encountered among patients on lithium therapy and their management, since lithium is still a fundamental and widely drug used in psychiatry and Internal Medicine.
PubMed database and Google scholar were used to search for relevant English language articles relating to lithium therapy and thyroid abnormalities up to December 2012. The search terms used were lithium treatment, thyroid abnormalities, thyroid dysfunction, goitre, hypothyroidism, hyperthyroidism, thyrotoxicosis, autoimmune thyroiditis, lithium toxicity, treatment of affective disorders and depression and side effects of antipsychotic drugs. Reference lists of the identified articles were further used to identify other studies.
Lithium affects normal thyroid functioning through multiple mechanisms. At the cellular level, it decreases thyroid hormone synthesis and release. It also decreases peripheral deiodination of tetraiodothyronine (T4) or thyroxine by decreasing the activity of type I 5' de-iodinase enzyme. Hypothyroidism and goitre (clinically and/ultrasonographically detected) are the most prevalent thyroid abnormalities among patients on long term lithium therapy. Lithium induced hyperthyroidism is very infrequent. Lithium increases the propensity to thyroid autoimmunity in susceptible individuals due to its effect of augmenting the activity of B lymphocytes and reducing the ratio of circulating suppressor to cytotoxic T cells.
Thyroid function tests (serum thyroid stimulating hormone, free thyroid hormones-T4 and triiodothyronine [T3] concentrations and thyroid auto-antibodies) and assessment of thyroid size clinically and by thyroid ultrasonography ought to be performed among patients initiating lithium therapy at baseline and later annually. More frequent assessment of thyroid function status and size during the course of therapy is recommended among middle aged females (≥50 years), patients with a family history of thyroid disease and those positive for thyroid auto-antibodies (anti-thyroid peroxidase and TSH receptor antibodies).
锂盐是用于治疗急性躁狂症、单相和双相抑郁症以及双相情感障碍预防的重要药物。迄今为止,医学文献中已广泛报道了与锂盐治疗相关的甲状腺异常情况。这些异常包括甲状腺肿、甲状腺功能减退、甲状腺功能亢进和自身免疫性甲状腺炎。鉴于锂盐仍是精神病学和内科中一种基本且广泛使用的药物,本综述探讨了接受锂盐治疗的患者中经常出现的各种甲状腺异常情况及其管理方法。
利用PubMed数据库和谷歌学术搜索截至2012年12月与锂盐治疗和甲状腺异常相关的英文文章。使用的搜索词包括锂盐治疗、甲状腺异常、甲状腺功能障碍、甲状腺肿、甲状腺功能减退、甲状腺功能亢进、甲状腺毒症、自身免疫性甲状腺炎、锂盐毒性、情感障碍和抑郁症的治疗以及抗精神病药物的副作用。已识别文章的参考文献列表进一步用于识别其他研究。
锂盐通过多种机制影响正常甲状腺功能。在细胞水平上,它会减少甲状腺激素的合成和释放。它还通过降低I型5'脱碘酶的活性来减少四碘甲状腺原氨酸(T4)或甲状腺素的外周脱碘。甲状腺功能减退和甲状腺肿(临床和/或超声检查发现)是长期接受锂盐治疗的患者中最常见的甲状腺异常情况。锂盐诱发的甲状腺功能亢进非常罕见。由于锂盐具有增强B淋巴细胞活性和降低循环抑制性T细胞与细胞毒性T细胞比例的作用,它会增加易感个体发生甲状腺自身免疫的倾向。
对于开始接受锂盐治疗的患者,应在基线时进行甲状腺功能检查(血清促甲状腺激素、游离甲状腺激素 - T4和三碘甲状腺原氨酸[T3]浓度以及甲状腺自身抗体),并在临床上和通过甲状腺超声检查评估甲状腺大小,之后每年进行一次。对于中年女性(≥50岁)、有甲状腺疾病家族史的患者以及甲状腺自身抗体(抗甲状腺过氧化物酶和促甲状腺激素受体抗体)呈阳性的患者,建议在治疗过程中更频繁地评估甲状腺功能状态和大小。