Gottwald-Hostalek Ulrike, Tayrouz Yorki
Merck Healthcare KGaA, Darmstadt, Germany.
Curr Med Res Opin. 2024 Dec;40(12):2109-2116. doi: 10.1080/03007995.2024.2435460. Epub 2024 Dec 3.
There remains considerable interest in the therapeutic use of combinations of levothyroxine (LT4) and triiodothyronine (liothyronine, T3) in the management of hypothyroidism, especially where hypothyroid-like symptoms persist on optimised LT4 monotherapy. This interest appears to be increasing, despite the lack of consistent identification of clinical benefit in people with hypothyroidism in randomised trials going back two decades. Guidelines support an individualised trial of addition of T3 to LT4 for symptomatic patients on optimised LT4. A new generation of clinical trials seeks to address this issue, using thyroid-specific instruments to measure patient-reported outcomes, among other innovations. Safety is the other critical element of the therapeutic profile of a drug. In this article, we review the safety of treatment LT4 + T3, with an emphasis on side-effects suggestive of thyrotoxicosis (overtreatment with thyroid hormones). Randomised trials that evaluated LT4 + T3 did not raise clear or consistent safety issues with this treatment. This was despite the use of regimens with a lower ratio of LT4:T3 (usually 4-10:1) than recommended currently by clinical experts in the field. In addition, a real-world analysis of side-effects of a commercial LT4 + T3 treatment (LT4:T3 ratio 5:1) that were reported spontaneously to a pharmacovigilance database revealed a low rate of reports, both overall and with regard to symptoms possible reminiscent of thyrotoxicosis. Safety concerns regarding the possibility of iatrogenic thyrotoxicosis appear unlikely to limit the future guideline-driven therapeutic use of LT4:T3 combinations with a ratio of these ingredients of around 15:1.
左甲状腺素(LT4)与三碘甲状腺原氨酸(碘塞罗宁,T3)联合用于治疗甲状腺功能减退症,仍然备受关注,尤其是在优化的LT4单药治疗后仍有甲状腺功能减退样症状持续存在的情况下。尽管在过去二十年的随机试验中,甲状腺功能减退症患者缺乏一致的临床获益证据,但这种关注似乎在增加。指南支持对接受优化LT4治疗的有症状患者进行个体化试验,在LT4基础上加用T3。新一代临床试验试图解决这一问题,采用甲状腺特异性工具来测量患者报告的结局等创新方法。安全性是药物治疗特征的另一个关键要素。在本文中,我们回顾了LT4 + T3治疗的安全性,重点关注提示甲状腺毒症(甲状腺激素过度治疗)的副作用。评估LT4 + T3的随机试验并未发现这种治疗存在明确或一致的安全问题。尽管使用的治疗方案中LT4与T3的比例(通常为4 - 10:1)低于该领域临床专家目前推荐的比例。此外,对一个药物警戒数据库自发报告的一种商业LT4 + T3治疗(LT4:T3比例为5:1)的副作用进行的真实世界分析显示,总体报告率较低,且与可能提示甲状腺毒症的症状相关的报告率也较低。关于医源性甲状腺毒症可能性的安全担忧似乎不太可能限制未来指南驱动的LT4:T3联合治疗的应用,其中这些成分的比例约为15:1。