Quality of life in Barth syndrome

Author:

Kim Alexander Y.1ORCID,Vernon Hilary2,Manuel Ryan3,Almuqbil Mohammed4,Hornby Brittany5ORCID

Affiliation:

1. Division of Genetics, Johns Hopkins All Children’s Hospital, St. Petersburg, FL, USA

2. Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USADepartment of Neurogenetics, Kennedy Krieger Institute, Baltimore, MD, USA

3. Department of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA

4. College of Medicine, King Saud Bin Abdulaziz University for Health Sciences (KSAU-HS), Riyadh, Saudi ArabiaDivision of Pediatric Neurology, King Abdullah Specialist Children’s Hospital (KASCH), National Guard Health Affairs (NGHA), Riyadh, Saudi ArabiaKing Abdullah International Medical Research Center (KAIMRC), Ministry of National Guard, Riyadh, Saudi Arabia

5. Physical Therapy Department, Kennedy Krieger Institute, 801 N Broadway, Baltimore, MD 21205, USA

Abstract

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 (PedsQLTM) Version 4.0 Generic Core Scales, PedsQLTM Multidimensional Fatigue Scale, Barth Syndrome Symptom Assessment, the PROMISTM Fatigue Short Form, the EuroQol Group EQ-5DTM, 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 PedsQLTM 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

Publisher

SAGE Publications

Subject

General Materials Science

Reference38 articles.

1. Online Mendelian Inheritance in Man, OMIM® (MIM Number # 302060). Baltimore, MD: Johns Hopkins University, 25 September 2018, https://omim.org/

2. A Bayesian Analysis to Determine the Prevalence of Barth Syndrome in the Pediatric Population

3. Barth syndrome: Clinical features and confirmation of gene localisation to distal Xq28

4. Online Mendelian Inheritance in Man, OMIM® (MIM Number * 300394). Baltimore, MD: Johns Hopkins University, 13 July 2018, https://omim.org/

5. Characterization of pain in patients with Barth syndrome

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3