Rett综合征和相关疾病的首要护理者关注点:来自美国自然史研究的数据。

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY Journal of Neurodevelopmental Disorders Pub Date : 2023-10-13 DOI:10.1186/s11689-023-09502-z
Jeffrey L Neul, Timothy A Benke, Eric D Marsh, Bernhard Suter, Lori Silveira, Cary Fu, Sarika U Peters, Alan K Percy
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摘要

目的:最近对Rett综合征(RTT)等神经发育障碍的理解取得了进展,从而发现了需要正式临床疗效评估的新治疗方法。临床试验的成功取决于评估对受影响个体影响最大的临床特征的结果指标。为了确定RTT和RTT相关疾病的首要关注点,我们要求护理人员列出护理人员的首要关注问题,以指导制定和选择针对这些疾病的适当临床试验结果指标。方法:参与美国RTT和RTT相关疾病自然史研究的参与者的护理人员(n = 925)被要求确定影响受影响参与者的前3个问题。我们为每种诊断类别生成了一份护理人员最关心的问题的加权列表,并比较了疾病之间的结果。此外,对于经典RTT,根据年龄、临床严重程度和MECP2中常见的RTT引起突变来分析护理人员的担忧。结果:经典RTT的主要护理人员担忧是有效沟通、癫痫发作、行走/平衡问题、缺乏手部使用和便秘。经典RTT的主要护理者关注的频率因年龄、临床严重程度和特定突变而异,与这些领域临床特征频率的已知变化一致。癫痫发作严重程度增加的参与者的护理人员通常将癫痫发作列为首要问题,而没有活动性癫痫发作的参与者的照顾人员通常将用手或交流列为首要关注。疾病之间的比较发现,经典RTT、非典型RTT、MECP2重复综合征、CDKL5缺乏症和FOXG1综合征之间的主要照顾者关注点存在共性;然而,这些疾病在照顾者关注方面的明显差异与特定临床特征的相对流行率和影响是一致的。结论:RTT和RTT相关疾病患者最关心的护理问题反映了这些疾病的主要临床症状的影响。这项工作对于开发有意义的疗法至关重要,因为最佳疗法应该解决这些问题。此外,临床试验中使用的结果指标应评估护理人员最关心的这些临床问题。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Top caregiver concerns in Rett syndrome and related disorders: data from the US natural history study.

Objective: Recent advances in the understanding of neurodevelopmental disorders such as Rett syndrome (RTT) have enabled the discovery of novel therapeutic approaches that require formal clinical evaluation of efficacy. Clinical trial success depends on outcome measures that assess clinical features that are most impactful for affected individuals. To determine the top concerns in RTT and RTT-related disorders we asked caregivers to list the top caregiver concerns to guide the development and selection of appropriate clinical trial outcome measures for these disorders.

Methods: Caregivers of participants enrolled in the US Natural History Study of RTT and RTT-related disorders (n = 925) were asked to identify the top 3 concerning problems impacting the affected participant. We generated a weighted list of top caregiver concerns for each of the diagnostic categories and compared results between the disorders. Further, for classic RTT, caregiver concerns were analyzed by age, clinical severity, and common RTT-causing mutations in MECP2.

Results: The top caregiver concerns for classic RTT were effective communication, seizures, walking/balance issues, lack of hand use, and constipation. The frequency of the top caregiver concerns for classic RTT varied by age, clinical severity, and specific mutations, consistent with known variation in the frequency of clinical features across these domains. Caregivers of participants with increased seizure severity often ranked seizures as the first concern, whereas caregivers of participants without active seizures often ranked hand use or communication as the top concern. Comparison across disorders found commonalities in the top caregiver concerns between classic RTT, atypical RTT, MECP2 duplication syndrome, CDKL5 deficiency disorder, and FOXG1 syndrome; however, distinct differences in caregiver concerns between these disorders are consistent with the relative prevalence and impact of specific clinical features.

Conclusion: The top caregiver concerns for individuals with RTT and RTT-related disorders reflect the impact of the primary clinical symptoms of these disorders. This work is critical in the development of meaningful therapies, as optimal therapy should address these concerns. Further, outcome measures to be utilized in clinical trials should assess these clinical issues identified as most concerning by caregivers.

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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
期刊最新文献
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