Literature DB >> 9972670

Role of colestipol in the treatment of hyperthyroidism.

P Hagag1, H Nissenbaum, M Weiss.   

Abstract

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.

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Year:  1998        PMID: 9972670     DOI: 10.1007/BF03348036

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN: 0391-4097            Impact factor:   4.256


  27 in total

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Authors:  A Shiroozu; K Okamura; H Ikenoue; K Sato; T Nakashima; M Yoshinari; M Fujishima; T Yoshizumi
Journal:  J Clin Endocrinol Metab       Date:  1986-07       Impact factor: 5.958

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Authors:  H R Superko; P Greenland; R A Manchester; N A Andreadis; G Schectman; N H West; D Hunninghake; W L Haskell; J L Probstfield
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7.  Kinetics of [123I]iodide uptake and discharge by perchlorate in studies of inhibition of iodide binding by antithyroid drugs.

Authors:  D C McCruden; T E Hilditch; J M Connell; W D Alexander
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8.  Apparent reduced absorption of gemfibrozil when given with colestipol.

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Journal:  J Clin Pharmacol       Date:  1990-01       Impact factor: 3.126

9.  The significance of the initial FT4-index for the management of single daily dose methimazole treatment of hyperthyroidism.

Authors:  A B Arntzenius; J W Elte; M Frölich; A Haak
Journal:  Clin Endocrinol (Oxf)       Date:  1988-09       Impact factor: 3.478

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Authors:  J L Witztum; L S Jacobs; G Schonfeld
Journal:  J Clin Endocrinol Metab       Date:  1978-05       Impact factor: 5.958

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4.  Clinical Trial of Four Weeks of Combination Therapy with Low-dose Methimazole and a Cholesterol Absorption Inhibitor as the Initial Treatment for Childhood-onset Graves' Disease.

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