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The impact of demographic and clinical characteristics on the trajectories of health-related quality of life among patients with Fabry disease

BACKGROUND: Fabry disease (FD) is an X-linked lysosomal storage disorder characterized by multiorgan dysfunction. Since individuals with FD usually experience progressive clinical disease manifestations, their health-related quality of life (HRQOL) is expected to change over time. However, there is...

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Autores principales: Sigurdardottir, Solrun, Bjerkely, Birgitte, Jenssen, Trond G., Mathisen, Per, von der Lippe, Charlotte, Ørstavik, Kristin, Heimdal, Ketil, Dahle, Dag Olav, Weedon-Fekjær, Mina Susanne, Solberg, Olga, Pihlstrøm, Hege K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506470/
https://www.ncbi.nlm.nih.gov/pubmed/34641933
http://dx.doi.org/10.1186/s13023-021-02066-y
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author Sigurdardottir, Solrun
Bjerkely, Birgitte
Jenssen, Trond G.
Mathisen, Per
von der Lippe, Charlotte
Ørstavik, Kristin
Heimdal, Ketil
Dahle, Dag Olav
Weedon-Fekjær, Mina Susanne
Solberg, Olga
Pihlstrøm, Hege K.
author_facet Sigurdardottir, Solrun
Bjerkely, Birgitte
Jenssen, Trond G.
Mathisen, Per
von der Lippe, Charlotte
Ørstavik, Kristin
Heimdal, Ketil
Dahle, Dag Olav
Weedon-Fekjær, Mina Susanne
Solberg, Olga
Pihlstrøm, Hege K.
author_sort Sigurdardottir, Solrun
collection PubMed
description BACKGROUND: Fabry disease (FD) is an X-linked lysosomal storage disorder characterized by multiorgan dysfunction. Since individuals with FD usually experience progressive clinical disease manifestations, their health-related quality of life (HRQOL) is expected to change over time. However, there is limited longitudinal research examining HRQOL outcomes in individuals with FD. We aimed to: assess longitudinal outcomes in HRQOL in adults with FD; examine the physical- and mental HRQOL trajectories at the initial registration (baseline), 3–5 year, and 7–13 year follow-ups; and evaluate the possible associations of age, sex and medical complications with the physical- and mental HRQOL trajectories. METHODS: Forty-three individuals with FD (53% female) who were aged 18 to 81 years at baseline attended clinical follow-up visits between 2006 and 2020. Medical records were extracted retrospectively. Demographics and the 36-item Short-Form Health Survey (SF-36) were recorded at scheduled visits, except for the last data collection which was prospectively obtained in 2020. The physical (PCS) and mental (MCS) composite scores (SF-36) were chosen as outcome measures. RESULTS: The eight SF-36 domain scores were stable over a span of 13 years, and only physical- and social functioning domains worsened clinically over this follow-up period. Mean baseline SF-36 domain scores were all significantly lower (decreased HRQOL) in the FD sample compared with Norwegian population norms. Two hierarchical linear models were run to examine whether demographics and medical complications (measured at the last clinical visit) predicted physical and mental HRQOL trajectories. Age above 47 years (p < 0.001), male sex (p = 0.027), small fibre neuropathy (p < 0.001), renal dysfunction (p < 0.001), and cerebrovascular events (p = 0.003) were associated with lower HRQOL over time. No significant interactions were found between the time of follow up and the abovementioned predictors of HRQOL. CONCLUSIONS: Overall HRQOL trajectories remained stable between baseline, 3–5 year, and 7–13 year follow-ups, with the majority of individuals reporting decreased physical and mental HRQOL. Medical complications in combination with older age and male sex are important predictors of lower HRQOL in FD. Awareness of this relationship is valuable both for health care providers and for patients. The findings provide indicators that can guide treatment decisions to improve physical and mental HRQOL outcomes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-021-02066-y.
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spelling pubmed-85064702021-10-12 The impact of demographic and clinical characteristics on the trajectories of health-related quality of life among patients with Fabry disease Sigurdardottir, Solrun Bjerkely, Birgitte Jenssen, Trond G. Mathisen, Per von der Lippe, Charlotte Ørstavik, Kristin Heimdal, Ketil Dahle, Dag Olav Weedon-Fekjær, Mina Susanne Solberg, Olga Pihlstrøm, Hege K. Orphanet J Rare Dis Research BACKGROUND: Fabry disease (FD) is an X-linked lysosomal storage disorder characterized by multiorgan dysfunction. Since individuals with FD usually experience progressive clinical disease manifestations, their health-related quality of life (HRQOL) is expected to change over time. However, there is limited longitudinal research examining HRQOL outcomes in individuals with FD. We aimed to: assess longitudinal outcomes in HRQOL in adults with FD; examine the physical- and mental HRQOL trajectories at the initial registration (baseline), 3–5 year, and 7–13 year follow-ups; and evaluate the possible associations of age, sex and medical complications with the physical- and mental HRQOL trajectories. METHODS: Forty-three individuals with FD (53% female) who were aged 18 to 81 years at baseline attended clinical follow-up visits between 2006 and 2020. Medical records were extracted retrospectively. Demographics and the 36-item Short-Form Health Survey (SF-36) were recorded at scheduled visits, except for the last data collection which was prospectively obtained in 2020. The physical (PCS) and mental (MCS) composite scores (SF-36) were chosen as outcome measures. RESULTS: The eight SF-36 domain scores were stable over a span of 13 years, and only physical- and social functioning domains worsened clinically over this follow-up period. Mean baseline SF-36 domain scores were all significantly lower (decreased HRQOL) in the FD sample compared with Norwegian population norms. Two hierarchical linear models were run to examine whether demographics and medical complications (measured at the last clinical visit) predicted physical and mental HRQOL trajectories. Age above 47 years (p < 0.001), male sex (p = 0.027), small fibre neuropathy (p < 0.001), renal dysfunction (p < 0.001), and cerebrovascular events (p = 0.003) were associated with lower HRQOL over time. No significant interactions were found between the time of follow up and the abovementioned predictors of HRQOL. CONCLUSIONS: Overall HRQOL trajectories remained stable between baseline, 3–5 year, and 7–13 year follow-ups, with the majority of individuals reporting decreased physical and mental HRQOL. Medical complications in combination with older age and male sex are important predictors of lower HRQOL in FD. Awareness of this relationship is valuable both for health care providers and for patients. The findings provide indicators that can guide treatment decisions to improve physical and mental HRQOL outcomes. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-021-02066-y. BioMed Central 2021-10-12 /pmc/articles/PMC8506470/ /pubmed/34641933 http://dx.doi.org/10.1186/s13023-021-02066-y 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Sigurdardottir, Solrun
Bjerkely, Birgitte
Jenssen, Trond G.
Mathisen, Per
von der Lippe, Charlotte
Ørstavik, Kristin
Heimdal, Ketil
Dahle, Dag Olav
Weedon-Fekjær, Mina Susanne
Solberg, Olga
Pihlstrøm, Hege K.
The impact of demographic and clinical characteristics on the trajectories of health-related quality of life among patients with Fabry disease
title The impact of demographic and clinical characteristics on the trajectories of health-related quality of life among patients with Fabry disease
title_full The impact of demographic and clinical characteristics on the trajectories of health-related quality of life among patients with Fabry disease
title_fullStr The impact of demographic and clinical characteristics on the trajectories of health-related quality of life among patients with Fabry disease
title_full_unstemmed The impact of demographic and clinical characteristics on the trajectories of health-related quality of life among patients with Fabry disease
title_short The impact of demographic and clinical characteristics on the trajectories of health-related quality of life among patients with Fabry disease
title_sort impact of demographic and clinical characteristics on the trajectories of health-related quality of life among patients with fabry disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506470/
https://www.ncbi.nlm.nih.gov/pubmed/34641933
http://dx.doi.org/10.1186/s13023-021-02066-y
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