Development of the APBD-SQ, a novel patient-reported outcome for health-related quality of life in adult polyglucosan body disease

被引:0
|
作者
Wilson, Genevieve E. [1 ]
Goldman, Deberah S. [2 ]
Saxe, Harriet [2 ]
Li, Xiaochun [3 ]
Goldberg, Judith D. [3 ]
Lau, Heather A. [1 ]
Abreu, Nicolas J. [1 ]
机构
[1] NYU, Dept Neurol, Div Neurogenet, Grossman Sch Med, New York, NY USA
[2] Adult Polyglucosan Body Dis Res Fdn, Brooklyn, NY USA
[3] NYU, Grossman Sch Med, Dept Populat Hlth, Div Biostat, New York, NY USA
基金
美国国家卫生研究院;
关键词
Adult Polyglucosan body disease; Health-related quality of life; Disease severity; Patient-reported outcomes;
D O I
10.1016/j.jns.2024.123168
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Adult polyglucosan body disease (APBD) is a rare autosomal recessive glycogen storage disorder that leads to slowly progressive multi-organ dysfunction in adulthood. A novel disease-specific patient-reported outcome measure was created and administered to assess symptom burden and health-related quality of life (HR-QOL) in APBD. Thirty-six participants between 30 and 79 years of age (83% >= 60 years, 56% male) completed the anonymous questionnaire independently or with a caregiver proxy (75% self-report). Unemployment predicted an 18.3 (95% CI: 2.8, 33.8; p = 0.028) higher composite disease severity score and a 28.8 (95% CI: 8.2, 49.4; p = 0.010) higher composite HR-QOL score. Use of one or more assistive devices also predicted a 29.3 (95% CI: 8.3, 50.4; p = 0.011) higher composite disease severity score and a 41.8 (95% CI: 10.9, 72.8; p = 0.013) higher composite HR-QOL score. Proxy survey completion predicted a 19.4 (95% CI: 4.1, 34.7; p = 0.020) higher composite disease severity score compared to self-report. Older age at survey completion predicted a 27.4 higher composite HR-QOL score (95% CI: 2.5, 52.4; p = 0.039) for participants in their sixties compared to those between 30 and 59 years old. The development of the Adult Polyglucosan Body Disease questionnaire on Symptom burden and health-related Quality of life (APBD-SQ) marks an important stride forward in capturing the patient experience as a tool for disease monitoring and future research.
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页数:8
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