Home LiteratureArticle Details
PMID: 1986725 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Initial therapy of patients with Wilson's disease with tetrathiomolybdate.

Archives of neurology ·Vol. 48 ·No. 1 ·1991-01-00 ·Pages 42-7

Brewer GJ, Dick RD, Yuzbasiyan-Gurkin V, Tankanow R, Young AB, Kluin KJ

Abstract

Patients with Wilson's disease who present with acute neurological symptoms often become clinically worse when initially treated with penicillamine. Other available anticopper drug therapies do not appear to offer a solution to this treatment problem. We are developing and evaluating a new drug, ammonium tetrathiomolybdate for this purpose. Theoretically, tetrathiomolybdate has optimal properties, including an immediate blockade of copper absorption and the property of forming complexes with copper in the blood, rendering the copper nontoxic. In this article, we present results from six patients treated with tetrathiomolybdate for up to 8 weeks as initial therapy. None of the five patients who had presented with acute neurological symptoms worsened. Also presented are methods of assay, preliminary stability studies, and methods of evaluating therapeutic end points with respect to copper metabolism.

MeSH Terms
Adolescent Adult Ceruloplasmin/metabolism Copper/metabolism Female Hepatolenticular Degeneration/drug therapy,metabolism Humans Male Molybdenum/therapeutic use
Chemicals
Copper Molybdenum tetrathiomolybdate Ceruloplasmin
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Brewer G J
Department of Human Genetics, University of Michigan, Ann Arbor 48109-0618.
Dick R D
Yuzbasiyan-Gurkin V
Tankanow R
Young A B
Kluin K J
Article Info
Journal
Archives of neurology
Abbr.
Arch Neurol
ISSN
0003-9942
Published
1991-01-00
Pages
42-7
Language
English
Region
United States
NLM ID
0372436
Subset
IM
Grants
FDA HHS · FD-U-000505 · United States
CMHS SAMHSA HHS · SM01-FR-42 · United States
Corrections
CommentIn
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