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Quality of life and its predictors in adults with tuberous sclerosis complex (TSC): a multicentre cohort study from Germany
BACKGROUND: Tuberous sclerosis complex (TSC) is a monogenetic, multisystemic disease characterised by the formation of benign tumours that can affect almost all organs, caused by pathogenic variations in TSC1 or TSC2. In this multicentre study from Germany, we investigated the influence of sociodemo...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237479/ https://www.ncbi.nlm.nih.gov/pubmed/34176514 http://dx.doi.org/10.1186/s42466-021-00130-3 |
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author | Zöllner, Johann Philipp Conradi, Nadine Sauter, Matthias Knuf, Markus Knake, Susanne Kurlemann, Gerhard Mayer, Thomas Hertzberg, Christoph Bertsche, Astrid Immisch, Ilka Klein, Karl Martin Marquard, Klaus Meyer, Sascha Noda, Anna H. von Podewils, Felix Schäfer, Hannah Thiels, Charlotte Zukunft, Bianca Schubert-Bast, Susanne Grau, Janina Willems, Laurent M. Rosenow, Felix Reese, Jens-Peter Strzelczyk, Adam |
author_facet | Zöllner, Johann Philipp Conradi, Nadine Sauter, Matthias Knuf, Markus Knake, Susanne Kurlemann, Gerhard Mayer, Thomas Hertzberg, Christoph Bertsche, Astrid Immisch, Ilka Klein, Karl Martin Marquard, Klaus Meyer, Sascha Noda, Anna H. von Podewils, Felix Schäfer, Hannah Thiels, Charlotte Zukunft, Bianca Schubert-Bast, Susanne Grau, Janina Willems, Laurent M. Rosenow, Felix Reese, Jens-Peter Strzelczyk, Adam |
author_sort | Zöllner, Johann Philipp |
collection | PubMed |
description | BACKGROUND: Tuberous sclerosis complex (TSC) is a monogenetic, multisystemic disease characterised by the formation of benign tumours that can affect almost all organs, caused by pathogenic variations in TSC1 or TSC2. In this multicentre study from Germany, we investigated the influence of sociodemographic, clinical, and therapeutic factors on quality of life (QoL) among individuals with TSC. METHODS: We assessed sociodemographic and clinical characteristics and QoL among adults with TSC throughout Germany using a validated, three-month, retrospective questionnaire. We examined predictors of health-related QoL (HRQoL) using multiple linear regression analysis and compared the QoL among patients with TSC with QoL among patients with other chronic neurological disorders. RESULTS: We enrolled 121 adults with TSC (mean age: 31.0 ± 10.5 years; range: 18–61 years, 45.5% [n = 55] women). Unemployment, a higher grade of disability, a higher number of organ manifestations, the presence of neuropsychiatric manifestations or active epilepsy, and a higher burden of therapy-related adverse events were associated with worse QoL, as measured by two QoL instruments (EuroQoL-5 dimensions [EQ-5D] and Quality of Life in Epilepsy Patients [QOLIE-31]). Neuropsychiatric and structural nervous system manifestations, the number of affected organs, and therapy-related adverse events were also associated with higher depression, as measured by the Neurological Disorders Depression Inventory for Epilepsy (NDDI-E). In multiple regression analysis, more severe therapy-related adverse events (large effect, p < 0.001), active epilepsy (large effect, p < 0.001), and neuropsychiatric manifestations (medium effect, p = 0.003) were independently associated with worse HRQoL, explaining 65% of the variance (p < 0.001). The HRQoL among patients with active TSC-associated epilepsy was worse than that among patients with drug-refractory mesial temporal lobe epilepsy (p < 0.001), and the generic QoL among patients with more than three TSC organ manifestations was similar to those of patients with severe migraine and uncontrolled asthma. CONCLUSIONS: Active epilepsy, neuropsychiatric manifestations (such as anxiety and depression), and therapy-related adverse events are important independent predictors of worse quality of life among adults with TSC. Generic quality of life in TSC with several manifestations is similar to uncontrolled severe chronic diseases and significantly negatively correlates with TSC severity. TRIAL REGISTRATION: DRKS, DRKS00016045. Registered 01 March 2019. |
format | Online Article Text |
id | pubmed-8237479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-82374792021-06-29 Quality of life and its predictors in adults with tuberous sclerosis complex (TSC): a multicentre cohort study from Germany Zöllner, Johann Philipp Conradi, Nadine Sauter, Matthias Knuf, Markus Knake, Susanne Kurlemann, Gerhard Mayer, Thomas Hertzberg, Christoph Bertsche, Astrid Immisch, Ilka Klein, Karl Martin Marquard, Klaus Meyer, Sascha Noda, Anna H. von Podewils, Felix Schäfer, Hannah Thiels, Charlotte Zukunft, Bianca Schubert-Bast, Susanne Grau, Janina Willems, Laurent M. Rosenow, Felix Reese, Jens-Peter Strzelczyk, Adam Neurol Res Pract Research Article BACKGROUND: Tuberous sclerosis complex (TSC) is a monogenetic, multisystemic disease characterised by the formation of benign tumours that can affect almost all organs, caused by pathogenic variations in TSC1 or TSC2. In this multicentre study from Germany, we investigated the influence of sociodemographic, clinical, and therapeutic factors on quality of life (QoL) among individuals with TSC. METHODS: We assessed sociodemographic and clinical characteristics and QoL among adults with TSC throughout Germany using a validated, three-month, retrospective questionnaire. We examined predictors of health-related QoL (HRQoL) using multiple linear regression analysis and compared the QoL among patients with TSC with QoL among patients with other chronic neurological disorders. RESULTS: We enrolled 121 adults with TSC (mean age: 31.0 ± 10.5 years; range: 18–61 years, 45.5% [n = 55] women). Unemployment, a higher grade of disability, a higher number of organ manifestations, the presence of neuropsychiatric manifestations or active epilepsy, and a higher burden of therapy-related adverse events were associated with worse QoL, as measured by two QoL instruments (EuroQoL-5 dimensions [EQ-5D] and Quality of Life in Epilepsy Patients [QOLIE-31]). Neuropsychiatric and structural nervous system manifestations, the number of affected organs, and therapy-related adverse events were also associated with higher depression, as measured by the Neurological Disorders Depression Inventory for Epilepsy (NDDI-E). In multiple regression analysis, more severe therapy-related adverse events (large effect, p < 0.001), active epilepsy (large effect, p < 0.001), and neuropsychiatric manifestations (medium effect, p = 0.003) were independently associated with worse HRQoL, explaining 65% of the variance (p < 0.001). The HRQoL among patients with active TSC-associated epilepsy was worse than that among patients with drug-refractory mesial temporal lobe epilepsy (p < 0.001), and the generic QoL among patients with more than three TSC organ manifestations was similar to those of patients with severe migraine and uncontrolled asthma. CONCLUSIONS: Active epilepsy, neuropsychiatric manifestations (such as anxiety and depression), and therapy-related adverse events are important independent predictors of worse quality of life among adults with TSC. Generic quality of life in TSC with several manifestations is similar to uncontrolled severe chronic diseases and significantly negatively correlates with TSC severity. TRIAL REGISTRATION: DRKS, DRKS00016045. Registered 01 March 2019. BioMed Central 2021-06-28 /pmc/articles/PMC8237479/ /pubmed/34176514 http://dx.doi.org/10.1186/s42466-021-00130-3 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 | Research Article Zöllner, Johann Philipp Conradi, Nadine Sauter, Matthias Knuf, Markus Knake, Susanne Kurlemann, Gerhard Mayer, Thomas Hertzberg, Christoph Bertsche, Astrid Immisch, Ilka Klein, Karl Martin Marquard, Klaus Meyer, Sascha Noda, Anna H. von Podewils, Felix Schäfer, Hannah Thiels, Charlotte Zukunft, Bianca Schubert-Bast, Susanne Grau, Janina Willems, Laurent M. Rosenow, Felix Reese, Jens-Peter Strzelczyk, Adam Quality of life and its predictors in adults with tuberous sclerosis complex (TSC): a multicentre cohort study from Germany |
title | Quality of life and its predictors in adults with tuberous sclerosis complex (TSC): a multicentre cohort study from Germany |
title_full | Quality of life and its predictors in adults with tuberous sclerosis complex (TSC): a multicentre cohort study from Germany |
title_fullStr | Quality of life and its predictors in adults with tuberous sclerosis complex (TSC): a multicentre cohort study from Germany |
title_full_unstemmed | Quality of life and its predictors in adults with tuberous sclerosis complex (TSC): a multicentre cohort study from Germany |
title_short | Quality of life and its predictors in adults with tuberous sclerosis complex (TSC): a multicentre cohort study from Germany |
title_sort | quality of life and its predictors in adults with tuberous sclerosis complex (tsc): a multicentre cohort study from germany |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8237479/ https://www.ncbi.nlm.nih.gov/pubmed/34176514 http://dx.doi.org/10.1186/s42466-021-00130-3 |
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