Clinical Endocrinology Branch, National Institute of Diabetes & Digestive & Kidney Diseases, National Institutes of Health, Building 10, CRC, RM 6-3940, 10 Center Drive, MSC 1613, Bethesda, MD 20892-1613, USA.
Clin Endocrinol (Oxf). 2010 May;72(5):709-15. doi: 10.1111/j.1365-2265.2009.03700.x.
The substitution of liothyronine (L-T3) for levothyroxine (L-T4) is commonly employed during thyroid hormone (TH) withdrawal in preparation for diagnostic and therapeutic interventions on thyroid cancer patients. Presently, only limited data are available on the L-T3 for L-T4 therapeutic substitution. Objective To characterize the pharmcodynamic equivalence of L-T3 and L-T4.
Randomized, double-blind, cross-over intervention study.
NIH clinical center.
Ten thyroidectomized patients.
Study participants were treated with L-T3 or L-T4 with a target TSH >or= 0.5 <or= 1.5 mU/l for at least 30 days before undergoing inpatient testing. Following testing, subjects crossed-over according to the same scheme.
Area under the serum concentration-time curve of TSH from 0 to 60 min (AUC(0-60)) and peak TSH serum concentration (C(max)) following thyrotropin-releasing hormone (TRH) stimulation test, total L-T4 and L-T3 dose (mcg/kg), and L-T4/L-T3 ratio.
No difference was observed for time 0 TSH values between L-T3 and L-T4 replacement phases (1.48 +/- 0.77 vs. 1.21 +/- 0.62 mU/l, P = 0.293) at average daily doses of 40.3 +/- 11.3 mcg L-T3 and 115.2 +/- 38.5 mcg L-T4, L-T3: L-T4 ratio 0.36 +/- 0.06. TRH stimulation test resulted in similar L-T3 vs. L-T4 TSH responses with AUC(0-60) of 326.1 (95% CI 232.6-457.1) and 247.1 (95% CI 153.8-397.1) mU* min/l (P = 0.285); and C(max) of 6.83 (95% CI 4.88-9.55) and 5.23 (95% CI 3.31-8.3) mU/l (P = 0.383).
This is the first study addressing the equivalency between L-T3 and L-T4 therapy measured by baseline and TRH-stimulated TSH. The therapeutic substitution of L-T3 for L-T4 was achieved at approximately 1:3 ratio.
在甲状腺激素(TH)停药期间,为准备甲状腺癌患者的诊断和治疗干预,常将三碘甲状腺原氨酸(L-T3)替代左甲状腺素(L-T4)。目前,关于 L-T3 替代 L-T4 的治疗仅有有限的数据。目的 描述 L-T3 和 L-T4 的药效学等效性。
随机、双盲、交叉干预研究。
NIH 临床中心。
10 例甲状腺切除术患者。
研究参与者接受 L-T3 或 L-T4 治疗,目标 TSH >0.5 <1.5 mU/l,至少 30 天,然后进行住院检查。检查后,根据相同方案进行交叉。
从 0 到 60 分钟的血清 TSH 浓度-时间曲线下面积(AUC(0-60))和促甲状腺激素释放激素(TRH)刺激试验后 TSH 血清浓度的峰值(C(max)),总 L-T4 和 L-T3 剂量(mcg/kg),以及 L-T4/L-T3 比值。
在平均每日剂量为 40.3 ± 11.3 mcg L-T3 和 115.2 ± 38.5 mcg L-T4 时,L-T3 和 L-T4 替代阶段的 0 时 TSH 值无差异(1.48 ± 0.77 对 1.21 ± 0.62 mU/l,P = 0.293),L-T3:L-T4 比值 0.36 ± 0.06。TRH 刺激试验导致 L-T3 与 L-T4 的 TSH 反应相似,AUC(0-60)分别为 326.1(95%CI 232.6-457.1)和 247.1(95%CI 153.8-397.1)mU*min/L(P = 0.285);C(max)分别为 6.83(95%CI 4.88-9.55)和 5.23(95%CI 3.31-8.3)mU/L(P = 0.383)。
这是第一项通过基础和 TRH 刺激 TSH 来评估 L-T3 和 L-T4 治疗等效性的研究。L-T3 替代 L-T4 的治疗达到了约 1:3 的比值。