Literature DB >> 24356057

Worsening of Wilson disease following penicillamine therapy.

Jayantee Kalita1, Vijay Kumar, Satish Chandra, Bishwanath Kumar, Usha Kant Misra.   

Abstract

BACKGROUND: Penicillamine is a standard therapy for Wilson disease (WD) but some patients have paradoxical worsening. Predictors of such deterioration have not been evaluated. This study documents frequency and predictors of deterioration following treatment in WD.
METHODS: 59 consecutive patients with neurologic WD and 4 asymptomatic siblings were prospectively evaluated. Their clinical, laboratory, ultrasound abdomen and cranial MRI findings with and without worsening were compared. Patients were treated with oral penicillamine and/or zinc and followed up at 1, 3 and 6 months or earlier if needed. Deterioration was defined by >10% worsening in baseline Burke-Fahn-Marsden score or appearance of new neurological sign.
RESULTS: Patients' median age was 13 years and 13 were females. 19 patients (30.2%) worsened following treatment; 10 within 1 month, 7 in 1-3 months, and 2 after 3 months of treatment. Deterioration was associated with drooling, leukopenia, thrombocytopenia, splenomegaly and evidence of chronic liver disease. None of the asymptomatic patients following zinc therapy deteriorated.
CONCLUSIONS: In the deteriorating group, withdrawal of penicillamine resulted in improvement/stabilization in 11 patients, 2 improved by trientine therapy and 4 continued to deteriorate till 3 months. 30.2% patients with WD deteriorated following penicillamine, especially those with chronic liver disease, leukopenia and thrombocytopenia.
© 2013 S. Karger AG, Basel.

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Year:  2013        PMID: 24356057     DOI: 10.1159/000355276

Source DB:  PubMed          Journal:  Eur Neurol        ISSN: 0014-3022            Impact factor:   1.710


  23 in total

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Review 2.  Clinical management of Wilson disease.

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

Review 3.  Neurologic impairment in Wilson disease.

Authors:  Petr Dusek; Tomasz Litwin; Anna Członkowska
Journal:  Ann Transl Med       Date:  2019-04

4.  Movement Disorder in Wilson Disease: Correlation with MRI and Biomarkers of Cell Injury.

Authors:  Jayantee Kalita; Vijay Kumar; Usha K Misra; Sunil Kumar
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5.  Memory and Learning Dysfunction Following Copper Toxicity: Biochemical and Immunohistochemical Basis.

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Journal:  Mol Neurobiol       Date:  2017-05-23       Impact factor: 5.590

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

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Journal:  Neuromolecular Med       Date:  2015-07-30       Impact factor: 3.843

7.  A Study on Apoptosis and Anti-apoptotic Status in Wilson Disease.

Authors:  J Kalita; V Kumar; U K Misra
Journal:  Mol Neurobiol       Date:  2015-12-08       Impact factor: 5.590

8.  Persistence with medical treatment for Wilson disease in China based on a single center's survey research.

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9.  Oromandibular Dystonia in Wilson's Disease.

Authors:  Jayantee Kalita; Abhay Ranjan; Usha K Misra
Journal:  Mov Disord Clin Pract       Date:  2015-05-09

Review 10.  D-Penicillamine: The State of the Art in Humans and in Dogs from a Pharmacological and Regulatory Perspective.

Authors:  Michela Pugliese; Vito Biondi; Enrico Gugliandolo; Patrizia Licata; Alessio Filippo Peritore; Rosalia Crupi; Annamaria Passantino
Journal:  Antibiotics (Basel)       Date:  2021-05-28
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