Department of Cardiology and Institute of Vascular Medicine, Peking University Third Hospital, Key Laboratory of Molecular Cardiovascular Science, Ministry of Education, Beijing, China.
Department of Cardiology, State Key Laboratory of Cardiovascular Disease, Fuwai Hospital, National Center for Cardiovascular Diseases, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.
Cell Rep Med. 2024 Apr 16;5(4):101473. doi: 10.1016/j.xcrm.2024.101473. Epub 2024 Mar 26.
We report a randomized, multicenter, open-label trial (ClinicalTrials.gov: NCT03096613) to investigate the clinical benefits of levothyroxine (L-T4) administration in subclinical hypothyroidism (SCH) patients with heart failure with reduced ejection fraction (HFrEF). Overall, 117 patients were enrolled and received L-T4 plus standard HFrEF treatment (experimental group, N = 57) or standard HFrEF therapy alone (control group, N = 60). The change of 6-min walk test distance in the experimental group was significantly higher than that in the control group at 24 weeks (70.08 ± 85.76 m vs. 27.73 ± 82.00 m, mean difference [95% confidence interval (CI)] 46.90 [12.90, 80.90], p < 0.001). Improvements in New York Heart Association (NYHA) classification (p = 0.033) and thyroid function were significant. Adverse event incidence was similar between groups (risk ratio [95% CI]: 0.942 1.053 (0.424, 2.616); p = 0.628). L-T4 addition to HFrEF treatment improved activity tolerance, NYHA class, and thyroid function within 6 months, suggesting its potential for combined therapy in HFrEF patients with SCH. Future double-blind, placebo-controlled trials should be performed to confirm these results.
我们报告了一项随机、多中心、开放标签试验(ClinicalTrials.gov:NCT03096613),旨在研究左甲状腺素(L-T4)在伴有射血分数降低的心力衰竭(HFrEF)的亚临床甲状腺功能减退症(SCH)患者中的临床获益。共有 117 名患者入组并接受 L-T4 加标准 HFrEF 治疗(实验组,N=57)或标准 HFrEF 单独治疗(对照组,N=60)。在 24 周时,实验组 6 分钟步行试验距离的变化明显高于对照组(70.08±85.76 m 比 27.73±82.00 m,平均差值[95%置信区间(CI)] 46.90[12.90, 80.90],p<0.001)。纽约心脏协会(NYHA)分级(p=0.033)和甲状腺功能的改善也具有显著意义。两组间不良事件发生率相似(风险比[95%CI]:0.942 1.053(0.424, 2.616);p=0.628)。在 6 个月内,L-T4 联合 HFrEF 治疗可改善活动耐量、NYHA 分级和甲状腺功能,提示其在 SCH 合并 HFrEF 患者中的联合治疗潜力。未来应进行双盲、安慰剂对照试验以确认这些结果。