Hagag P, Nissenbaum H, Weiss M
Endocrine Institute, Assaf Harofeh Medical Centre, Zerifin, Israel.
J Endocrinol Invest. 1998 Dec;21(11):725-31. doi: 10.1007/BF03348036.
The enterohepatic circulation of thyroxine (T4) and triiodothyronine (T3) is higher in thyrotoxicosis. Bile-salt sequestrants bind iodothyronines and thereby increase their fecal excretion. We, therefore, evaluated the effect of colestipol-hydrochloride administration on clinical and biochemical indices of patients with hyperthyroidism. In a prospective, controlled trial, ninety-two adult volunteers with Graves' disease, toxic autonomous nodule or toxic multinodular goiter were randomly assigned into the following treatment protocols: Group 1, 30 mg of methimazole (MMI) and 20 g of colestipol-hydrochloride (COL) daily; Group 2, 30 mg of MMI daily; and Group 3, 15 mg of MMI 20 g of COL daily. The patients were further classified into Group A, severe hyperthyroidism (baseline levels of total T3 (TT3) > or =5 nmol/l) and Group B, mild to moderate thyrotoxicosis (baseline levels of TT-3<5 nmol/l). Crook's clinical index, serum free T4 (FT4), TT3 and thyroid stimulating hormone (TSH) levels were determined before (WO), following one week (W1) and two weeks (W2) of treatment. Serum TT3 level decreased (mean+/-SE) at W1 by 40.8+/-2.6% of WO in Group1 and by 29.2+/-2.4% in Group 2 (p<0.001), and down further to 47.8+/-3.0% at W2 in Group 1, and 40.6+/-2.8% in Group 2 (p=0.01). Serum FT4 level decreased (mean+/-SE) from WO to W1 by 31.7+/-2.7% in Group 1 and by 16.2+/-3.1% in Group 2 (p=0.005), and down to 49.1+/-2.8% of WO at W2 in Group 1 and to 38.7+/-3.5% in Group 2 (p=0.07). In sub groups B COL was not effective in reducing thyroid hormone levels nor in ameliorating the clinical status of the patients. However, in Group A3 COL lowered FT4 (p=0.001) and TT3 (p=0.05) levels as compared to group A2. At W2 the clinical hyperthyroidism score improved faster in Group A1 (p<0.001) and Group A3 (p=0.012) as compared to the control Group A2. In conclusion, COL is an effective and well tolerated adjunctive agent in the treatment of hyperthyroidism. Its main effect is in severe cases of thyrotoxicosis, and in the first phase of treatment. As adjunctive COL treatment in hyperthyroidism allows reducing MMI dosage it may decrease the rate of dose dependent MMI side effects.
甲状腺毒症患者中,甲状腺素(T4)和三碘甲状腺原氨酸(T3)的肠肝循环更为活跃。胆盐螯合剂可结合碘甲状腺原氨酸,从而增加其粪便排泄量。因此,我们评估了给予盐酸考来烯胺对甲状腺功能亢进患者临床及生化指标的影响。在一项前瞻性对照试验中,92名患有格雷夫斯病、毒性自主性结节或毒性多结节性甲状腺肿的成年志愿者被随机分配至以下治疗方案:第1组,每日服用30毫克甲巯咪唑(MMI)和20克盐酸考来烯胺(COL);第2组,每日服用30毫克MMI;第3组,每日服用15毫克MMI和20克COL。患者进一步分为A组,重度甲状腺功能亢进(总T3(TT3)基线水平≥5纳摩尔/升)和B组,轻度至中度甲状腺毒症(TT - 3基线水平<5纳摩尔/升)。在治疗前(W0)、治疗一周后(W1)和两周后(W2)测定克鲁克临床指数、血清游离T4(FT4)、TT3和促甲状腺激素(TSH)水平。第1组血清TT3水平在W1时下降(均值±标准误),较W0下降了40.8±2.6%,第2组下降了29.2±2.4%(p<0.001),第1组在W2时进一步降至47.8±3.0%,第2组降至40.6±2.8%(p = 0.01)。血清FT4水平从W0到W1,第1组下降了31.7±2.7%,第2组下降了16.2±3.1%(p = 0.005),第1组在W2时降至W0的49.1±2.8%,第2组降至38.7±3.5%(p = 0.07)。在B亚组中,COL在降低甲状腺激素水平及改善患者临床状态方面无效。然而,在A3组中,与A2组相比,COL降低了FT4(p = 0.001)和TT3(p = 0.05)水平。在W2时,与对照组A2相比,A1组(p<0.001)和A3组(p = 0.012)的临床甲状腺功能亢进评分改善更快。总之,COL是治疗甲状腺功能亢进有效且耐受性良好的辅助药物。其主要作用于重度甲状腺毒症病例及治疗的第一阶段。作为甲状腺功能亢进的辅助治疗,COL可减少MMI剂量,可能降低MMI剂量依赖性副作用的发生率。