Toward an Understanding of GSD5 (McArdle disease): How Do Individuals Learn to Live with the Metabolic Defect in Daily Life.

IF 3.2 4区 医学 Q2 CLINICAL NEUROLOGY
Walaa Karazi, Jacqueline Coppers, Daphne Maas, Edith Cup, Bart Bloemen, Nicole Voet, Jan T Groothuis, Tomàs Pinós, Ramon Marti Seves, Ros Quinlivan, Nicoline Løkken, John Vissing, Salman Bhai, Andrew Wakelin, Stacey Reason, Nicol C Voermans
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引用次数: 0

Abstract

Background: Glycogen storage disease type 5 (GSD) is an autosomal recessive inherited metabolic myopathy caused by a deficiency of the enzyme muscle glycogen phosphorylase. Individuals with GSD5 experience physical activity intolerance.

Objective: This patient-led study aimed to capture the daily life experiences of GSD5, with a focus on adapting to and coping with their physical activity intolerance.

Methods: An online survey was composed in close collaboration with patient organizations. It consisted of customized and validated questionnaires on demographics, general health and comorbidities, physical activity, psychosocial well-being and functioning, pain, fatigue and adapting to and coping with GSD5.

Results: One hundred sixty-two participants (16 countries) participated. The majority, n = 86 (69%) were from the Netherlands, USA or UK. We observed a high rate of misdiagnosis prior to GSD5 diagnosis (49%), surprisingly a relatively high proportion had not been diagnosed by DNA testing which is the gold standard. Being diagnosed had a strong impact on emotional status, daily life activities and important life choices. A large proportion had not received any rehabilitation (41%) nor medical treatment (57%) before diagnosis. Engagement in vigorous and moderate physical activity was reduced. Health related quality of life was low, most likely related to low physical health. The median Fatigue Severity Score was 4.3, indicating moderate to severe fatigue. Participants themselves had found various ways to adapt to and cope with their disability. The adaptations concerned all aspect of their life, including household chores, social and physical activities, and work. In addition to lack of support, participants reported limited availability of information sources.

Conclusion: Participants have provided guidance for newly diagnosed people, including the advice to accept one's limited abilities and maintain an active lifestyle. We conclude that adequate counseling on ways of adapting and coping is expected to increase both health-related quality of life and physical activity.

了解 GSD5(麦卡德尔病):个体如何学会在日常生活中与代谢缺陷共存。
背景:糖原贮积病 5 型(GSD)是一种常染色体隐性遗传代谢性肌病,由肌糖原磷酸化酶缺乏引起。GSD5患者会出现体力活动不耐受的症状:这项由患者主导的研究旨在了解 GSD5 患者的日常生活经历,重点关注他们如何适应和应对体力活动不耐受的问题:方法:我们与患者组织密切合作,编制了一份在线调查问卷。该调查由经过验证的定制问卷组成,内容涉及人口统计学、一般健康和合并症、体育活动、社会心理健康和功能、疼痛、疲劳以及适应和应对 GSD5:162 名参与者(16 个国家)参加了调查。结果: 16 个国家的 162 名参与者参加了此次活动,其中大多数(n = 86)(69%)来自荷兰、美国或英国。我们发现,在确诊 GSD5 之前,误诊率很高(49%),令人惊讶的是,没有通过 DNA 检测(黄金标准)确诊的比例相对较高。确诊对情绪状态、日常生活活动和重要的人生选择都有很大影响。很大一部分人在确诊前没有接受过任何康复治疗(41%)或药物治疗(57%)。参与剧烈和适度体育活动的比例下降。与健康相关的生活质量较低,这很可能与身体健康状况不佳有关。疲劳严重程度评分的中位数为 4.3,表明存在中度至重度疲劳。参与者自己找到了各种适应和应对残疾的方法。这些适应方法涉及他们生活的方方面面,包括家务、社交和体育活动以及工作。除了缺乏支持外,参与者还表示信息来源有限:结论:参与者为新确诊患者提供了指导,包括建议他们接受自己有限的能力并保持积极的生活方式。我们得出的结论是,就适应和应对方式提供适当的咨询有望提高与健康相关的生活质量和体育活动量。
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来源期刊
Journal of neuromuscular diseases
Journal of neuromuscular diseases Medicine-Neurology (clinical)
CiteScore
5.10
自引率
6.10%
发文量
102
期刊介绍: The Journal of Neuromuscular Diseases aims to facilitate progress in understanding the molecular genetics/correlates, pathogenesis, pharmacology, diagnosis and treatment of acquired and genetic neuromuscular diseases (including muscular dystrophy, myasthenia gravis, spinal muscular atrophy, neuropathies, myopathies, myotonias and myositis). The journal publishes research reports, reviews, short communications, letters-to-the-editor, and will consider research that has negative findings. The journal is dedicated to providing an open forum for original research in basic science, translational and clinical research that will improve our fundamental understanding and lead to effective treatments of neuromuscular diseases.
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