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Understanding the life experience of Barth syndrome from the perspective of adults: a qualitative one-on-one interview study
BACKGROUND: Barth syndrome (BTHS, OMIM 302060) is a rare, life-threatening, x-linked genetic disorder that occurs almost exclusively in males and is characterized by cardiomyopathy, neutropenia, skeletal muscle myopathy primarily affecting larger muscles, and shorter stature in youth. A greater numb...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836365/ https://www.ncbi.nlm.nih.gov/pubmed/31699126 http://dx.doi.org/10.1186/s13023-019-1200-8 |
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author | Mazar, Iyar Stokes, Jonathan Ollis, Sarah Love, Emily Espensen, Ashlee Barth, Peter G. Powers, John H. Shields, Alan L. |
author_facet | Mazar, Iyar Stokes, Jonathan Ollis, Sarah Love, Emily Espensen, Ashlee Barth, Peter G. Powers, John H. Shields, Alan L. |
author_sort | Mazar, Iyar |
collection | PubMed |
description | BACKGROUND: Barth syndrome (BTHS, OMIM 302060) is a rare, life-threatening, x-linked genetic disorder that occurs almost exclusively in males and is characterized by cardiomyopathy, neutropenia, skeletal muscle myopathy primarily affecting larger muscles, and shorter stature in youth. A greater number of individuals with BTHS are now surviving into adulthood due to advancements in diagnosis and disease management. Given these improvements in life expectancy, understanding the disease experience over time has become increasingly important to individuals with the condition, treatment developers, and regulatory agencies. A study was conducted to explore the experience of BTHS from the perspective of adult males at least 35 years of age with the condition via in-depth qualitative interviews. RESULTS: Findings showed that adults with BTHS experienced a variety of signs/symptoms with variable onset and severity throughout their lives, the most frequently reported being the symptoms of tiredness, muscle weakness, and a fast and/or irregular heart rate, and the sign of short stature in youth. These signs/symptoms negatively impacted individuals’ emotional, physical, social, and role functioning. Tiredness and weakness impacted some individuals’ physical functioning from an early age and into adulthood. These symptoms generally worsened over time, increasingly interfering with individuals’ ability to fully participate in paid and unpaid labor and to partake in family and leisure activities. CONCLUSIONS: This research complements recent studies characterizing the potentially degenerative and progressive nature of BTHS and can encourage future research into the natural history and progression of BTHS in untreated individuals. Participants’ interview responses revealed a range of symptoms and the potential for multiple impacts on individuals’ physical, social, emotional, and role functioning as a result of BTHS symptoms, yet also revealed variability in severity of experience as well as the possibility of resilience and adaptation to the condition. |
format | Online Article Text |
id | pubmed-6836365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-68363652019-11-08 Understanding the life experience of Barth syndrome from the perspective of adults: a qualitative one-on-one interview study Mazar, Iyar Stokes, Jonathan Ollis, Sarah Love, Emily Espensen, Ashlee Barth, Peter G. Powers, John H. Shields, Alan L. Orphanet J Rare Dis Research BACKGROUND: Barth syndrome (BTHS, OMIM 302060) is a rare, life-threatening, x-linked genetic disorder that occurs almost exclusively in males and is characterized by cardiomyopathy, neutropenia, skeletal muscle myopathy primarily affecting larger muscles, and shorter stature in youth. A greater number of individuals with BTHS are now surviving into adulthood due to advancements in diagnosis and disease management. Given these improvements in life expectancy, understanding the disease experience over time has become increasingly important to individuals with the condition, treatment developers, and regulatory agencies. A study was conducted to explore the experience of BTHS from the perspective of adult males at least 35 years of age with the condition via in-depth qualitative interviews. RESULTS: Findings showed that adults with BTHS experienced a variety of signs/symptoms with variable onset and severity throughout their lives, the most frequently reported being the symptoms of tiredness, muscle weakness, and a fast and/or irregular heart rate, and the sign of short stature in youth. These signs/symptoms negatively impacted individuals’ emotional, physical, social, and role functioning. Tiredness and weakness impacted some individuals’ physical functioning from an early age and into adulthood. These symptoms generally worsened over time, increasingly interfering with individuals’ ability to fully participate in paid and unpaid labor and to partake in family and leisure activities. CONCLUSIONS: This research complements recent studies characterizing the potentially degenerative and progressive nature of BTHS and can encourage future research into the natural history and progression of BTHS in untreated individuals. Participants’ interview responses revealed a range of symptoms and the potential for multiple impacts on individuals’ physical, social, emotional, and role functioning as a result of BTHS symptoms, yet also revealed variability in severity of experience as well as the possibility of resilience and adaptation to the condition. BioMed Central 2019-11-07 /pmc/articles/PMC6836365/ /pubmed/31699126 http://dx.doi.org/10.1186/s13023-019-1200-8 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Mazar, Iyar Stokes, Jonathan Ollis, Sarah Love, Emily Espensen, Ashlee Barth, Peter G. Powers, John H. Shields, Alan L. Understanding the life experience of Barth syndrome from the perspective of adults: a qualitative one-on-one interview study |
title | Understanding the life experience of Barth syndrome from the perspective of adults: a qualitative one-on-one interview study |
title_full | Understanding the life experience of Barth syndrome from the perspective of adults: a qualitative one-on-one interview study |
title_fullStr | Understanding the life experience of Barth syndrome from the perspective of adults: a qualitative one-on-one interview study |
title_full_unstemmed | Understanding the life experience of Barth syndrome from the perspective of adults: a qualitative one-on-one interview study |
title_short | Understanding the life experience of Barth syndrome from the perspective of adults: a qualitative one-on-one interview study |
title_sort | understanding the life experience of barth syndrome from the perspective of adults: a qualitative one-on-one interview study |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836365/ https://www.ncbi.nlm.nih.gov/pubmed/31699126 http://dx.doi.org/10.1186/s13023-019-1200-8 |
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