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Burden of disease in myasthenia gravis: taking the patient’s perspective
BACKGROUND: Myasthenia gravis (MG) leads to exertion-dependent muscle weakness, but also psychological and social well-being are limited. We aim to describe the burden of disease in MG including sociodemographic, economical, psychosocial as well as clinical aspects, to compare health-related quality...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer Berlin Heidelberg
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120127/ https://www.ncbi.nlm.nih.gov/pubmed/34800167 http://dx.doi.org/10.1007/s00415-021-10891-1 |
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author | Lehnerer, Sophie Jacobi, Jonas Schilling, Ralph Grittner, Ulrike Marbin, Derin Gerischer, Lea Stascheit, Frauke Krause, Maike Hoffmann, Sarah Meisel, Andreas |
author_facet | Lehnerer, Sophie Jacobi, Jonas Schilling, Ralph Grittner, Ulrike Marbin, Derin Gerischer, Lea Stascheit, Frauke Krause, Maike Hoffmann, Sarah Meisel, Andreas |
author_sort | Lehnerer, Sophie |
collection | PubMed |
description | BACKGROUND: Myasthenia gravis (MG) leads to exertion-dependent muscle weakness, but also psychological and social well-being are limited. We aim to describe the burden of disease in MG including sociodemographic, economical, psychosocial as well as clinical aspects, to compare health-related quality of life (HRQoL) of patients with MG to the general population (genP) and to explore risk factors for a lower HRQoL. METHODS: This case–control study was conducted with MG patients of the German Myasthenia Association. A questionnaire-based survey included sociodemographic and clinical data as well as standardized questionnaires, e.g. the Short Form Health (SF-36). HRQoL was compared to genP in a matched-pairs analysis. Participants of the German Health Interview and Examination Survey for Adults (DEGS1) served as control group. RESULTS: In our study, 1660 MG patients participated and were compared to 2556 controls from the genP. Patients with MG showed lower levels of physical functioning (SF-36 mean 56.0, SD 30.3) compared to the genP (mean 81.8, SD 22.1, adjusted difference: 25, 95% CI 22–29) and lower mental health sub-score (SF-36 mean 67.3, SD 19.8, vs. 74.1, SD 16.7, adjusted difference: 5, 95% CI 2–8). Female gender, higher age, low income, partnership status, lower activities of daily life, symptoms of depression, anxiety and fatigue and self-perceived low social support were associated with a lower HRQoL in MG patients. DISCUSSION: HRQoL is lower in patients with MG compared to genP. The burden of MG on patients includes economic and social aspects as well as their emotional well-being. New therapies must achieve improvements for patients in these areas. TRIAL REGISTRATION INFORMATION: Clinicaltrials.gov, NCT03979521, submitted: June 7, 2019, first patient enrolled: May 1, 2019, https://clinicaltrials.gov/ct2/show/NCT03979521 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-021-10891-1. |
format | Online Article Text |
id | pubmed-9120127 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-91201272022-05-21 Burden of disease in myasthenia gravis: taking the patient’s perspective Lehnerer, Sophie Jacobi, Jonas Schilling, Ralph Grittner, Ulrike Marbin, Derin Gerischer, Lea Stascheit, Frauke Krause, Maike Hoffmann, Sarah Meisel, Andreas J Neurol Original Communication BACKGROUND: Myasthenia gravis (MG) leads to exertion-dependent muscle weakness, but also psychological and social well-being are limited. We aim to describe the burden of disease in MG including sociodemographic, economical, psychosocial as well as clinical aspects, to compare health-related quality of life (HRQoL) of patients with MG to the general population (genP) and to explore risk factors for a lower HRQoL. METHODS: This case–control study was conducted with MG patients of the German Myasthenia Association. A questionnaire-based survey included sociodemographic and clinical data as well as standardized questionnaires, e.g. the Short Form Health (SF-36). HRQoL was compared to genP in a matched-pairs analysis. Participants of the German Health Interview and Examination Survey for Adults (DEGS1) served as control group. RESULTS: In our study, 1660 MG patients participated and were compared to 2556 controls from the genP. Patients with MG showed lower levels of physical functioning (SF-36 mean 56.0, SD 30.3) compared to the genP (mean 81.8, SD 22.1, adjusted difference: 25, 95% CI 22–29) and lower mental health sub-score (SF-36 mean 67.3, SD 19.8, vs. 74.1, SD 16.7, adjusted difference: 5, 95% CI 2–8). Female gender, higher age, low income, partnership status, lower activities of daily life, symptoms of depression, anxiety and fatigue and self-perceived low social support were associated with a lower HRQoL in MG patients. DISCUSSION: HRQoL is lower in patients with MG compared to genP. The burden of MG on patients includes economic and social aspects as well as their emotional well-being. New therapies must achieve improvements for patients in these areas. TRIAL REGISTRATION INFORMATION: Clinicaltrials.gov, NCT03979521, submitted: June 7, 2019, first patient enrolled: May 1, 2019, https://clinicaltrials.gov/ct2/show/NCT03979521 SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s00415-021-10891-1. Springer Berlin Heidelberg 2021-11-20 2022 /pmc/articles/PMC9120127/ /pubmed/34800167 http://dx.doi.org/10.1007/s00415-021-10891-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Original Communication Lehnerer, Sophie Jacobi, Jonas Schilling, Ralph Grittner, Ulrike Marbin, Derin Gerischer, Lea Stascheit, Frauke Krause, Maike Hoffmann, Sarah Meisel, Andreas Burden of disease in myasthenia gravis: taking the patient’s perspective |
title | Burden of disease in myasthenia gravis: taking the patient’s perspective |
title_full | Burden of disease in myasthenia gravis: taking the patient’s perspective |
title_fullStr | Burden of disease in myasthenia gravis: taking the patient’s perspective |
title_full_unstemmed | Burden of disease in myasthenia gravis: taking the patient’s perspective |
title_short | Burden of disease in myasthenia gravis: taking the patient’s perspective |
title_sort | burden of disease in myasthenia gravis: taking the patient’s perspective |
topic | Original Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9120127/ https://www.ncbi.nlm.nih.gov/pubmed/34800167 http://dx.doi.org/10.1007/s00415-021-10891-1 |
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