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Identifying trajectories of fatigue in patients with primary mitochondrial disease due to the m.3243A > G variant

Severe fatigue is a common complaint in patients with primary mitochondrial disease. However, less is known about the course of fatigue over time. This longitudinal observational cohort study of patients with the mitochondrial DNA 3243 A>G variant explored trajectories of fatigue over 2 years, an...

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Autores principales: Klein, Inge‐Lot, Verhaak, Christianne M., Smeitink, Jan A. M., de Laat, Paul, Janssen, Mirian C. H., Custers, José A. E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805089/
https://www.ncbi.nlm.nih.gov/pubmed/36053898
http://dx.doi.org/10.1002/jimd.12546
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author Klein, Inge‐Lot
Verhaak, Christianne M.
Smeitink, Jan A. M.
de Laat, Paul
Janssen, Mirian C. H.
Custers, José A. E.
author_facet Klein, Inge‐Lot
Verhaak, Christianne M.
Smeitink, Jan A. M.
de Laat, Paul
Janssen, Mirian C. H.
Custers, José A. E.
author_sort Klein, Inge‐Lot
collection PubMed
description Severe fatigue is a common complaint in patients with primary mitochondrial disease. However, less is known about the course of fatigue over time. This longitudinal observational cohort study of patients with the mitochondrial DNA 3243 A>G variant explored trajectories of fatigue over 2 years, and characteristics of patients within these fatigue trajectories. Fifty‐three adult patients treated at the Radboud University Medical Center Nijmegen were included. The majority of the patients reported consistent, severe fatigue (41%), followed by patients with a mixed pattern of severe and mild fatigue (36%). Then, 23% of patients reported stable mild fatigue levels. Patients with a stable high fatigue trajectory were characterized by higher disease manifestations scores, more clinically relevant mental health symptoms, and lower psychosocial functioning and quality of life compared to patients reporting stable low fatigue levels. Fatigue at baseline and disease manifestation scores predicted fatigue severity at the 2‐year assessment (57% explained variance). This study demonstrates that severe fatigue is a common and stable complaint in the majority of patients. Clinicians should be aware of severe fatigue in patients with moderate to severe disease manifestation scores on the Newcastle Mitochondrial Disease Scale, the high prevalence of clinically relevant mental health symptoms and overall impact on quality of life in these patients. Screening of fatigue and psychosocial variables will guide suitable individualized treatment to improve the quality of life.
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spelling pubmed-98050892023-01-06 Identifying trajectories of fatigue in patients with primary mitochondrial disease due to the m.3243A > G variant Klein, Inge‐Lot Verhaak, Christianne M. Smeitink, Jan A. M. de Laat, Paul Janssen, Mirian C. H. Custers, José A. E. J Inherit Metab Dis Original Articles Severe fatigue is a common complaint in patients with primary mitochondrial disease. However, less is known about the course of fatigue over time. This longitudinal observational cohort study of patients with the mitochondrial DNA 3243 A>G variant explored trajectories of fatigue over 2 years, and characteristics of patients within these fatigue trajectories. Fifty‐three adult patients treated at the Radboud University Medical Center Nijmegen were included. The majority of the patients reported consistent, severe fatigue (41%), followed by patients with a mixed pattern of severe and mild fatigue (36%). Then, 23% of patients reported stable mild fatigue levels. Patients with a stable high fatigue trajectory were characterized by higher disease manifestations scores, more clinically relevant mental health symptoms, and lower psychosocial functioning and quality of life compared to patients reporting stable low fatigue levels. Fatigue at baseline and disease manifestation scores predicted fatigue severity at the 2‐year assessment (57% explained variance). This study demonstrates that severe fatigue is a common and stable complaint in the majority of patients. Clinicians should be aware of severe fatigue in patients with moderate to severe disease manifestation scores on the Newcastle Mitochondrial Disease Scale, the high prevalence of clinically relevant mental health symptoms and overall impact on quality of life in these patients. Screening of fatigue and psychosocial variables will guide suitable individualized treatment to improve the quality of life. John Wiley & Sons, Inc. 2022-08-24 2022-11 /pmc/articles/PMC9805089/ /pubmed/36053898 http://dx.doi.org/10.1002/jimd.12546 Text en © 2022 The Authors. Journal of Inherited Metabolic Disease published by John Wiley & Sons Ltd on behalf of SSIEM. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Klein, Inge‐Lot
Verhaak, Christianne M.
Smeitink, Jan A. M.
de Laat, Paul
Janssen, Mirian C. H.
Custers, José A. E.
Identifying trajectories of fatigue in patients with primary mitochondrial disease due to the m.3243A > G variant
title Identifying trajectories of fatigue in patients with primary mitochondrial disease due to the m.3243A > G variant
title_full Identifying trajectories of fatigue in patients with primary mitochondrial disease due to the m.3243A > G variant
title_fullStr Identifying trajectories of fatigue in patients with primary mitochondrial disease due to the m.3243A > G variant
title_full_unstemmed Identifying trajectories of fatigue in patients with primary mitochondrial disease due to the m.3243A > G variant
title_short Identifying trajectories of fatigue in patients with primary mitochondrial disease due to the m.3243A > G variant
title_sort identifying trajectories of fatigue in patients with primary mitochondrial disease due to the m.3243a > g variant
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9805089/
https://www.ncbi.nlm.nih.gov/pubmed/36053898
http://dx.doi.org/10.1002/jimd.12546
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