Literature DB >> 26549350

Wilson disease: Health-related quality of life and risk for depression.

Mark Schaefer1, Daniel Nils Gotthardt1, Nicole Ganion2, Sascha Wohnsland3, Jessica Seessle1, Wolfgang Stremmel1, Jan Pfeiffenberger1, Karl Heinz Weiss4.   

Abstract

BACKGROUND: Wilson disease is an autosomal recessive disorder of copper metabolism and requires lifelong medical treatment. Therefore, the analysis of quality of life has gathered more attention. Aims of this study were to examine risk for depression and health-related quality of life in patients suffering from Wilson disease.
METHODS: Sixty-eight patients were included in this retrospective cross sectional study. The Personal Health Questionnaire-9 Depression Scale was used to assess depression. The Short Form-36 Health Survey questionnaire was used to assess health-related quality of life.
RESULTS: The Personal Health Questionnaire-9 indicated that 21% (14/68) of patients were at risk for major depressive disorders (scores>10) and 35% (24/68) were at risk for mild depression (scores 5-9). Women had significantly lower life quality scores than men. Primary neurologic disease manifestation was associated with significantly lower total Short Form-36 and subdimension scores compared with primary hepatic or mixed presentation. Overall, patients with Wilson disease experienced higher quality of life than patients with other chronic liver diseases.
CONCLUSIONS: As patients with Wilson disease have a high risk for depressive disorders, active assessment for depression is mandatory. Patients with primary neurological symptoms are at higher risk for reduction of life quality.
Copyright © 2015 Elsevier Masson SAS. All rights reserved.

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Year:  2015        PMID: 26549350     DOI: 10.1016/j.clinre.2015.09.007

Source DB:  PubMed          Journal:  Clin Res Hepatol Gastroenterol        ISSN: 2210-7401            Impact factor:   2.947


  5 in total

Review 1.  Wilson disease.

Authors:  Anna Członkowska; Tomasz Litwin; Petr Dusek; Peter Ferenci; Svetlana Lutsenko; Valentina Medici; Janusz K Rybakowski; Karl Heinz Weiss; Michael L Schilsky
Journal:  Nat Rev Dis Primers       Date:  2018-09-06       Impact factor: 52.329

Review 2.  The patient experience of Wilson disease: a conceptual model based on qualitative research.

Authors:  Stella Karantzoulis; Karli Heuer; Nicole Sparling; Megan Teynor
Journal:  Orphanet J Rare Dis       Date:  2021-10-19       Impact factor: 4.123

3.  Wilson disease in Northern Portugal: a long-term follow-up study.

Authors:  Isabel Garrido; Margarida Marques; Rodrigo Liberal; Hélder Cardoso; Susana Lopes; Guilherme Macedo
Journal:  Orphanet J Rare Dis       Date:  2022-02-23       Impact factor: 4.123

4.  Quality of Life in Wilson's Disease: A Systematic Literature Review.

Authors:  Chakrapani Balijepalli; Kevin Yan; Lakshmi Gullapalli; Stephane Barakat; Helene Chevrou-Severac; Eric Druyts
Journal:  J Health Econ Outcomes Res       Date:  2021-12-08

Review 5.  Patient and observer reported outcome measures to evaluate health-related quality of life in inherited metabolic diseases: a scoping review.

Authors:  Carlota Pascoal; Sandra Brasil; Rita Francisco; Dorinda Marques-da-Silva; Agnes Rafalko; Jaak Jaeken; Paula A Videira; Luísa Barros; Vanessa Dos Reis Ferreira
Journal:  Orphanet J Rare Dis       Date:  2018-11-28       Impact factor: 4.123

  5 in total

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