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Quality of life in Barth syndrome

INTRODUCTION: Barth syndrome (BTHS) is a rare X-linked disorder characterized by cardiomyopathy, neutropenia, growth abnormalities, and skeletal myopathy. There have been few studies investigating health-related quality of life (HRQoL) in this population. This study investigated the impact of BTHS o...

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Autores principales: Kim, Alexander Y., Vernon, Hilary, Manuel, Ryan, Almuqbil, Mohammed, Hornby, Brittany
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032447/
https://www.ncbi.nlm.nih.gov/pubmed/37180415
http://dx.doi.org/10.1177/26330040221093743
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author Kim, Alexander Y.
Vernon, Hilary
Manuel, Ryan
Almuqbil, Mohammed
Hornby, Brittany
author_facet Kim, Alexander Y.
Vernon, Hilary
Manuel, Ryan
Almuqbil, Mohammed
Hornby, Brittany
author_sort Kim, Alexander Y.
collection PubMed
description INTRODUCTION: Barth syndrome (BTHS) is a rare X-linked disorder characterized by cardiomyopathy, neutropenia, growth abnormalities, and skeletal myopathy. There have been few studies investigating health-related quality of life (HRQoL) in this population. This study investigated the impact of BTHS on HRQoL and select physiologic measures in affected boys and men. METHODS: In this study, we characterize HRQoL in boys and men with BTHS through cross-sectional analysis of a variety of outcome measures including the Pediatric Quality of Life Inventory (PedsQL(TM)) Version 4.0 Generic Core Scales, PedsQL(TM) Multidimensional Fatigue Scale, Barth Syndrome Symptom Assessment, the PROMIS(TM) Fatigue Short Form, the EuroQol Group EQ-5D(TM), the Patient Global Impression of Symptoms (PGIS), and the Caregiver Global Impression of Symptoms (CaGIS). For a specific subset of participants, physiologic data were available in addition to HRQoL data. RESULTS: For the PedsQL(TM) questionnaires, 18 unique child and parent reports were analyzed for children aged 5–18 years, and nine unique parent reports were analyzed for children aged 2–4 years. For the other HRQoL outcome measures and physiologic measurements, the data from 12 subjects (age range 12–35 years) were analyzed. Based on parent and child reports, HRQoL is significantly impaired in boys and men with BTHS, especially in school functioning and physical functioning. Parent and child reports of more severe fatigue are significantly correlated with more impaired HRQoL. When exploring the potential relationship between physiology and HRQoL, the CaGIS as a whole for pediatric subjects and individual questionnaire items from the PGIS and CaGIS for pediatric subjects assessing tiredness, muscle weakness, and muscle pain showed the strongest correlations. CONCLUSION: This study provides a unique characterization of the HRQoL in boys and men with BTHS using a variety of outcome measures, and it highlights the negative impact of fatigue and muscle weakness on HRQoL in BTHS. TRIAL REGISTRY NAME:: A Trial to Evaluate Safety, Tolerability and Efficacy of Elamipretide in Subjects with Barth Syndrome (TAZPOWER). https://clinicaltrials.gov/ct2/show/NCT03098797. Registration Number: NCT03098797
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spelling pubmed-100324472023-05-11 Quality of life in Barth syndrome Kim, Alexander Y. Vernon, Hilary Manuel, Ryan Almuqbil, Mohammed Hornby, Brittany Ther Adv Rare Dis Original Research INTRODUCTION: Barth syndrome (BTHS) is a rare X-linked disorder characterized by cardiomyopathy, neutropenia, growth abnormalities, and skeletal myopathy. There have been few studies investigating health-related quality of life (HRQoL) in this population. This study investigated the impact of BTHS on HRQoL and select physiologic measures in affected boys and men. METHODS: In this study, we characterize HRQoL in boys and men with BTHS through cross-sectional analysis of a variety of outcome measures including the Pediatric Quality of Life Inventory (PedsQL(TM)) Version 4.0 Generic Core Scales, PedsQL(TM) Multidimensional Fatigue Scale, Barth Syndrome Symptom Assessment, the PROMIS(TM) Fatigue Short Form, the EuroQol Group EQ-5D(TM), the Patient Global Impression of Symptoms (PGIS), and the Caregiver Global Impression of Symptoms (CaGIS). For a specific subset of participants, physiologic data were available in addition to HRQoL data. RESULTS: For the PedsQL(TM) questionnaires, 18 unique child and parent reports were analyzed for children aged 5–18 years, and nine unique parent reports were analyzed for children aged 2–4 years. For the other HRQoL outcome measures and physiologic measurements, the data from 12 subjects (age range 12–35 years) were analyzed. Based on parent and child reports, HRQoL is significantly impaired in boys and men with BTHS, especially in school functioning and physical functioning. Parent and child reports of more severe fatigue are significantly correlated with more impaired HRQoL. When exploring the potential relationship between physiology and HRQoL, the CaGIS as a whole for pediatric subjects and individual questionnaire items from the PGIS and CaGIS for pediatric subjects assessing tiredness, muscle weakness, and muscle pain showed the strongest correlations. CONCLUSION: This study provides a unique characterization of the HRQoL in boys and men with BTHS using a variety of outcome measures, and it highlights the negative impact of fatigue and muscle weakness on HRQoL in BTHS. TRIAL REGISTRY NAME:: A Trial to Evaluate Safety, Tolerability and Efficacy of Elamipretide in Subjects with Barth Syndrome (TAZPOWER). https://clinicaltrials.gov/ct2/show/NCT03098797. Registration Number: NCT03098797 SAGE Publications 2022-06-11 /pmc/articles/PMC10032447/ /pubmed/37180415 http://dx.doi.org/10.1177/26330040221093743 Text en © The Author(s), 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Research
Kim, Alexander Y.
Vernon, Hilary
Manuel, Ryan
Almuqbil, Mohammed
Hornby, Brittany
Quality of life in Barth syndrome
title Quality of life in Barth syndrome
title_full Quality of life in Barth syndrome
title_fullStr Quality of life in Barth syndrome
title_full_unstemmed Quality of life in Barth syndrome
title_short Quality of life in Barth syndrome
title_sort quality of life in barth syndrome
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10032447/
https://www.ncbi.nlm.nih.gov/pubmed/37180415
http://dx.doi.org/10.1177/26330040221093743
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