Treatment of Hypothyroidism that Contains Liothyronine is Associated with Reduced Risk of Dementia and Mortality.

IF 5.1
Fabyan Esberard de Lima Beltrão, Giulia Carvalhal, Vandrize Meneghini, Danielle Albino Rafael Matos, Daniele Carvalhal de Almeida Beltrão, Bruna Albino Rafael Matos Andrade, Fabyo Napoleão de Lima Beltrão, Helton Estrela Ramos, Miriam O Ribeiro, George Golovko, Matthew D Ettleson, Antonio C Bianco
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Abstract

Introduction: Standard levothyroxine (LT4) therapy may not fully address all risks associated with hypothyroidism-especially cognitive decline, dementia, and mortality-even when TSH levels are normalized. Observational studies link hypothyroidism to higher dementia rates; the role of LT4 plus liothyronine (T3) therapies remains uncertain.

Methods: This retrospective cohort study analyzed TriNetX data, comparing 1.26 million patients with hypothyroidism (on LT4, LT4+T3, or desiccated thyroid extract [DTE]) to 3.32 million controls. Outcomes included dementia, atrial fibrillation (AFib), and mortality over 20 years of follow-up. Propensity score matching (PSM) was used to balance covariates for age, sex, and comorbidities. Adjusted hazard ratios were obtained via Cox proportional hazard modeling. A parallel systematic review and meta-analysis of 12 studies evaluated dementia risk in hypothyroidism.

Results: Patients with hypothyroidism showed a ∼1.4-fold higher risk of dementia and a >2.0-fold increase in mortality-even with normal TSH-and these risks were most pronounced when TSH levels were off-target. A parallel meta-analysis indicated a 1.4-fold heightened dementia risk. In cohorts formed by PSM comparing LT4 monotherapy versus combination therapy, RR analysis indicated 27% and 31% lower dementia and mortality risks, respectively, with combination therapy. The adjusted Cox model (HR) showed 16% and 25% reductions in these outcomes for combination therapy patients.

Conclusion: Despite standard LT4 therapy, hypothyroidism remains associated with heightened risks of dementia and mortality. Adding T3 may more effectively mitigate these risks than LT4 alone, but further studies are needed to confirm the cognitive and survival benefits of T3-containing regimens.

含碘甲状腺原氨酸治疗甲状腺功能减退与降低痴呆和死亡率风险相关
标准左旋甲状腺素(LT4)治疗可能不能完全解决与甲状腺功能减退相关的所有风险,特别是认知能力下降、痴呆和死亡率,即使TSH水平正常。观察性研究将甲状腺功能减退与较高的痴呆率联系起来;LT4加碘甲状腺原氨酸(T3)治疗的作用仍不确定。方法:本回顾性队列研究分析TriNetX数据,比较126万甲状腺功能减退患者(LT4、LT4+T3或干燥甲状腺提取物[DTE])和332万对照。结果包括痴呆、房颤(AFib)和20年随访期间的死亡率。倾向评分匹配(PSM)用于平衡年龄、性别和合并症的协变量。通过Cox比例风险模型获得调整后的风险比。一项对12项研究的平行系统回顾和荟萃分析评估了甲状腺功能减退症的痴呆风险。结果:甲状腺功能减退患者患痴呆的风险高出1.4倍,死亡率高出2.0倍,即使TSH正常,这些风险在TSH水平偏离目标时最为明显。一项平行荟萃分析显示,痴呆风险增加了1.4倍。在PSM形成的队列中,比较LT4单药治疗与联合治疗,RR分析显示,联合治疗的痴呆和死亡风险分别降低27%和31%。调整后的Cox模型(HR)显示,联合治疗患者的这些结果降低了16%和25%。结论:尽管标准的LT4治疗,甲状腺功能减退仍然与痴呆和死亡率增加的风险相关。添加T3可能比单独使用LT4更有效地减轻这些风险,但需要进一步的研究来证实含有T3的方案对认知和生存的益处。
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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