Literature DB >> 31206982

Comparative effectiveness of common therapies for Wilson disease: A systematic review and meta-analysis of controlled studies.

Christian Appenzeller-Herzog1, Tim Mathes2, Marlies L S Heeres3, Karl Heinz Weiss4, Roderick H J Houwen3, Hannah Ewald1,5.   

Abstract

BACKGROUND & AIMS: Wilson disease (WD) is a rare disorder of copper metabolism. The objective of this systematic review was to determine the comparative effectiveness and safety of common treatments of WD.
METHODS: We included WD patients of any age or stage and the study drugs D-penicillamine, zinc salts, trientine and tetrathiomolybdate. The control could be placebo, no treatment or any other treatment. We included prospective, retrospective, randomized and non-randomized studies. We searched Medline and Embase via Ovid, the Cochrane Central Register of Controlled Trials, and screened reference lists of included articles. Where possible, we applied random-effects meta-analyses.
RESULTS: The 23 included studies reported on 2055 patients and mostly compared D-penicillamine to no treatment, zinc, trientine or succimer. One study compared tetrathiomolybdate and trientine. Post-decoppering maintenance therapy was addressed in one study only. Eleven of 23 studies were of low quality. When compared to no treatment, D-penicillamine was associated with a lower mortality (odds ratio 0.013; 95% CI 0.0010 to 0.17). When compared to zinc, there was no association with mortality (odds ratio 0.73; 95% CI 0.16 to 3.40) and prevention or amelioration of clinical symptoms (odds ratio 0.84; 95% CI 0.48 to 1.48). Conversely, D-penicillamine may have a greater impact on side effects and treatment discontinuations than zinc.
CONCLUSIONS: There are some indications that zinc is safer than D-penicillamine therapy while being similarly effective in preventing or reducing hepatic or neurological WD symptoms. Study quality was low warranting cautious interpretation of our findings.
© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Wilson disease; hepatolenticular degeneration; meta-analysis; systematic review

Year:  2019        PMID: 31206982     DOI: 10.1111/liv.14179

Source DB:  PubMed          Journal:  Liver Int        ISSN: 1478-3223            Impact factor:   5.828


  7 in total

1.  Orphan Drug Use in Patients With Rare Diseases: A Population-Based Cohort Study.

Authors:  Francesca Gorini; Michele Santoro; Anna Pierini; Lorena Mezzasalma; Silvia Baldacci; Elena Bargagli; Alessandra Boncristiano; Maurizia Rossana Brunetto; Paolo Cameli; Francesco Cappelli; Giancarlo Castaman; Barbara Coco; Maria Alice Donati; Renzo Guerrini; Silvia Linari; Vittoria Murro; Iacopo Olivotto; Paola Parronchi; Francesca Pochiero; Oliviero Rossi; Barbara Scappini; Andrea Sodi; Alessandro Maria Vannucchi; Alessio Coi
Journal:  Front Pharmacol       Date:  2022-05-16       Impact factor: 5.988

2.  Switching Pharmacological Treatment in Wilson Disease: Case Report and Recommendations.

Authors:  Marcia Leung; Jaimie Wu Lanzafame; Valentina Medici
Journal:  J Investig Med High Impact Case Rep       Date:  2020 Jan-Dec

3.  Comparison of the Effectiveness and Safety of d-Penicillamine and Zinc Salt Treatment for Symptomatic Wilson Disease: A Systematic Review and Meta-Analysis.

Authors:  Shan Tang; Li Bai; Wei Hou; Zhongjie Hu; Xinyue Chen; Jing Zhao; Chen Liang; Wei Zhang; Zhongping Duan; Sujun Zheng
Journal:  Front Pharmacol       Date:  2022-03-18       Impact factor: 5.810

4.  Effect of oral zinc regimens on human hepatic copper content: a randomized intervention study.

Authors:  Ditte Emilie Munk; Tea Lund Laursen; Frederik Teicher Kirk; Hendrik Vilstrup; Aftab Ala; Lars Christian Gormsen; Peter Ott; Thomas Damgaard Sandahl
Journal:  Sci Rep       Date:  2022-08-29       Impact factor: 4.996

Review 5.  The Role of Zinc in the Treatment of Wilson's Disease.

Authors:  Abolfazl Avan; Anna Członkowska; Susan Gaskin; Alberto Granzotto; Stefano L Sensi; Tjaard U Hoogenraad
Journal:  Int J Mol Sci       Date:  2022-08-18       Impact factor: 6.208

6.  Designing Clinical Trials in Wilson's Disease.

Authors:  Peter Ott; Aurélia Poujois; Thomas Damgaard Sandahl; Karl Heinz Weiss; Peter Ferenci; Michael L Schilsky; Aftab Ala; Frederick K Askari; Anna Czlonkowska; Ralf-Dieter Hilgers; Eve A Roberts
Journal:  Hepatology       Date:  2021-10-05       Impact factor: 17.298

7.  Ammonium tetrathiomolybdate in the decoppering phase treatment of Wilson's disease with neurological symptoms: A case series.

Authors:  Oriol De Fabregues; Jaume Viñas; Antoni Palasí; Manuel Quintana; Ignasi Cardona; Cristina Auger; Víctor Vargas
Journal:  Brain Behav       Date:  2020-03-22       Impact factor: 2.708

  7 in total

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