Literature DB >> 19595438

Treatment of Wilson's disease with tetrathiomolybdate: V. Control of free copper by tetrathiomolybdate and a comparison with trientine.

George J Brewer1, Fred Askari, Robert B Dick, Julia Sitterly, John K Fink, Martha Carlson, Karen J Kluin, Matthew T Lorincz.   

Abstract

It has become clear that serum "free" copper (the copper not bound to ceruloplasmin in the blood) is the copper causing copper toxicity in Wilson's disease. But up until now, free copper has not been closely followed during initiation of anticopper therapy in neurologically presenting patients. During this period of initial therapy, the future fate of these patients hangs in the balance-if they worsen neurologically as often happens with penicillamine or trientine therapy, many never recover. We hypothesize that free copper levels are a biological marker of clinical outcome in these patients. In this article, we evaluate the control of free copper in 3 studies of initial anticopper treatment in neurologically presenting Wilson's disease patients. The first (study 1) is a 55-patient open-label trial of tetrathiomolybdate, the second (study 2) is a 48-patient double-blind trial comparing tetrathiomolybdate and trientine, and the third (study 3) is a 40-patient double-blind comparison of 2 disease regimens of tetrathiomolybdate. Free copper levels were determined by subtracting ceruloplasmin and tetrathiomolybdate bound copper from total serum copper. Tetrathiomolybdate showed very strong control of free copper levels over the 8 weeks of treatment in the 55-patient open-label study (study 1), reducing it to a mean value of about one fourth, or less, of baseline. In the tetrathiomolybdate/trientine double blind (study 2), tetrathiomolybdate again showed good control of free copper levels over 8 weeks of treatment, which is significantly better than trientine. In the trientine arm of study 2, mean free copper levels actually went up during trientine therapy. The 5 patients who neurologically worsened on trientine therapy over 8 weeks of treatment showed significant spikes in serum free copper levels associated in time with their neurologic worsening. Patients who did not worsen neurologically generally did not show significant spikes in free copper. Tetrathiomolybdate controlled copper less well in the dose regimen study (study 3) than in the previous 2 studies of tetrathiomolybdate treatment, probably because of a change in the way "away from food" tetrathiomolybdate was given.

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Year:  2009        PMID: 19595438     DOI: 10.1016/j.trsl.2009.05.002

Source DB:  PubMed          Journal:  Transl Res        ISSN: 1878-1810            Impact factor:   7.012


  43 in total

1.  Wilson disease: Canadian perspectives on presentation and outcomes from an adult ambulatory setting.

Authors:  A Moores; Susan Fox; Anthony Lang; Gideon M Hirschfield
Journal:  Can J Gastroenterol       Date:  2012-06       Impact factor: 3.522

2.  Wilson's disease: A review of what we have learned.

Authors:  Kryssia Isabel Rodriguez-Castro; Francisco Javier Hevia-Urrutia; Giacomo Carlo Sturniolo
Journal:  World J Hepatol       Date:  2015-12-18

Review 3.  Wilson disease-treatment perspectives.

Authors:  Tomasz Litwin; Karolina Dzieżyc; Anna Członkowska
Journal:  Ann Transl Med       Date:  2019-04

Review 4.  Clinical management of Wilson disease.

Authors:  Peter Hedera
Journal:  Ann Transl Med       Date:  2019-04

Review 5.  Copper suppression as cancer therapy: the rationale for copper chelating agents in BRAFV600 mutated melanoma.

Authors:  Sarah Sammons; Donita Brady; Linda Vahdat; April Ks Salama
Journal:  Melanoma Manag       Date:  2016-09-02

6.  Wilson disease: At the crossroads between genetics and epigenetics-A review of the evidence.

Authors:  Dorothy A Kieffer; Valentina Medici
Journal:  Liver Res       Date:  2017-08-16

7.  Characterization of a versatile organometallic pro-drug (CORM) for experimental CO based therapeutics.

Authors:  João D Seixas; Abhik Mukhopadhyay; Teresa Santos-Silva; Leo E Otterbein; David J Gallo; Sandra S Rodrigues; Bruno H Guerreiro; Ana M L Gonçalves; Nuno Penacho; Ana R Marques; Ana C Coelho; Patrícia M Reis; Maria J Romão; Carlos C Romão
Journal:  Dalton Trans       Date:  2013-05-07       Impact factor: 4.390

8.  Role of Oxidative Stress in the Worsening of Neurologic Wilson Disease Following Chelating Therapy.

Authors:  Jayantee Kalita; Vijay Kumar; Abhay Ranjan; Usha K Misra
Journal:  Neuromolecular Med       Date:  2015-07-30       Impact factor: 3.843

9.  Clinical efficacy of combined sodium dimercaptopropanesulfonate and zinc treatment in neurological Wilson's disease with D-penicillamine treatment failure.

Authors:  Dingbang Chen; Xiangxue Zhou; Haiman Hou; Li Feng; JunXiu Liu; Yinyin Liang; Xiaopu Lin; Jiwei Zhang; Chao Wu; Xiuling Liang; Zhong Pei; Xunhua Li
Journal:  Ther Adv Neurol Disord       Date:  2016-04-07       Impact factor: 6.570

10.  Molybdenum.

Authors:  Janet A Novotny; Catherine A Peterson
Journal:  Adv Nutr       Date:  2018-05-01       Impact factor: 8.701

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