Department of Endocrinology and Metabolism, John Hopkins University, 1830 East Monument Street, Suite 333, Baltimore, Maryland 21287-0003, USA.
J Clin Endocrinol Metab. 2010 Mar;95(3):1349-54. doi: 10.1210/jc.2009-1209. Epub 2010 Jan 15.
Widespread thyroid hormone actions offer the possibility of developing selective thyromimetic analogs with salutary metabolic properties. Consequently, effects of diiodothyropropionic acid (DITPA) on body weight, serum lipoproteins, and bone metabolism markers were studied in a prospective, controlled, double-blind 24-wk trial, which was primarily designed to assess treatment of stable chronic heart failure.
Eighty-six patients (aged 66 +/- 11 yr, mean +/- sd) were randomized (1:2) to placebo or an escalating DITPA dose (90 to 180, 270, and 360 mg/d) over 8 wk until serum TSH was less than 0.02 mU/liter. Patients were studied at 2, 4, 6, 8, 16, and 24 wk and after 4 wk off study drug. Only 21 DITPA-treated and 27 placebo patients completed the full 24 wk of therapy.
DITPA therapy lowered serum TSH levels and, to a lesser extent, serum T(3) and T(4), but there were no differences in clinical manifestations of thyrotoxicosis or hypothyroidism. Serum total and low-density lipoprotein cholesterol levels both decreased on DITPA; there was a transient decrease in triglycerides and no change in high-density lipoprotein cholesterol. DITPA therapy was associated with significant reduction in body weight, 12.5 lb at 24 wk. Increases in serum osteocalcin, N-telopeptide, and deoxypyridinoline levels were consistent with increased bone turnover on DITPA.
This investigation of DITPA actions demonstrated its efficacy in reducing body weight and lowering total and low-density lipoprotein cholesterol levels. However, DITPA's adverse effects at doses used resulted in a high dropout rate and potentially dangerous skeletal actions were observed.
广泛的甲状腺激素作用提供了开发具有有益代谢特性的选择性甲状腺模拟物的可能性。因此,研究了二碘甲状腺原氨酸丙酸(DITPA)对体重、血清脂蛋白和骨代谢标志物的影响,这是一项前瞻性、对照、双盲 24 周试验,主要旨在评估稳定慢性心力衰竭的治疗。
86 名患者(年龄 66 +/- 11 岁,平均值 +/- 标准差)被随机分为安慰剂组或递增剂量的 DITPA 组(90 至 180、270 和 360 mg/d),持续 8 周,直到血清 TSH 小于 0.02 mU/liter。患者在第 2、4、6、8、16 和 24 周以及停药 4 周后进行研究。只有 21 名 DITPA 治疗患者和 27 名安慰剂患者完成了完整的 24 周治疗。
DITPA 治疗降低了血清 TSH 水平,在较小程度上降低了血清 T(3)和 T(4)水平,但没有甲状腺毒症或甲状腺功能减退的临床表现差异。DITPA 治疗使血清总胆固醇和低密度脂蛋白胆固醇水平降低;甘油三酯短暂降低,高密度脂蛋白胆固醇无变化。DITPA 治疗与体重显著减轻相关,24 周时减轻 12.5 磅。血清骨钙素、N-末端肽和脱氧吡啶啉水平的增加与 DITPA 引起的骨转换增加一致。
本研究证明了 DITPA 在降低体重和降低总胆固醇和低密度脂蛋白胆固醇水平方面的有效性。然而,在使用的剂量下,DITPA 的不良反应导致高退出率,并观察到潜在危险的骨骼作用。