Developmental milestones and daily living skills in individuals with Angelman syndrome.

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY
Anjali Sadhwani, Sonya Powers, Anne Wheeler, Hillary Miller, Sarah Nelson Potter, Sarika U Peters, Carlos A Bacino, Steven A Skinner, Logan K Wink, Craig A Erickson, Lynne M Bird, Wen-Hann Tan
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Abstract

Background: Angelman syndrome (AS) is a neurodevelopmental disorder associated with severe global developmental delay. However, the ages at which different developmental skills are achieved in these individuals remain unclear. We seek to determine the probability and the age of acquisition of specific developmental milestones and daily living skills in individuals with AS across the different molecular subtypes, viz. class I deletion, class II deletion, uniparental disomy, imprinting defect, and UBE3A variants.

Methods: Caregivers participating in a longitudinal multicenter Angelman Syndrome Natural History Study completed a questionnaire regarding the age at which their children achieved specific developmental milestones and daily living skills. The Cox Proportional Hazard model was applied to analyze differences in the probability of achievement of skills at various ages among five molecular subtypes of AS.

Results: Almost all individuals, regardless of molecular subtype, were able to walk with support by five years of age. By age 15, those with a deletion had at least a 50% probability of acquiring 17 out of 30 skills compared to 25 out of 30 skills among those without a deletion. Overall, fine and gross motor skills such as holding and reaching for small objects, sitting, and walking with support were achieved within a fairly narrow range of ages, while toileting, feeding, and hygiene skills tend to have greater variability in the ages at which these skills were achieved. Those without a deletion had a higher probability (25-92%) of achieving daily living skills such as independently toileting and dressing compared to those with a deletion (0-13%). Across all molecular subtypes, there was a low probability of achieving independence in bathing and brushing teeth.

Conclusion: Individuals with AS without a deletion are more likely to achieve developmental milestones and daily living skills at an earlier age than those with a deletion. Many individuals with AS are unable to achieve daily living skills necessary for independent self-care.

安杰曼综合症患者的发育里程碑和日常生活技能。
背景介绍安杰尔曼综合征(AS)是一种与严重的全面发育迟缓有关的神经发育障碍。然而,这些患者获得不同发育技能的年龄仍不清楚。我们试图确定不同分子亚型(即 I 类缺失、II 类缺失、单亲裂殖、印记缺陷和 UBE3A 变异)的 AS 患者获得特定发育里程碑和日常生活技能的概率和年龄:参加多中心安杰尔曼综合征自然史纵向研究的照顾者填写了一份关于其子女达到特定发育里程碑和日常生活技能的年龄的调查问卷。研究人员采用 Cox 比例危险模型分析了五种分子亚型 AS 患者在不同年龄阶段掌握技能的概率差异:结果:无论分子亚型如何,几乎所有患者在五岁前都能在支撑物的帮助下行走。到15岁时,基因缺失者至少有50%的可能性掌握30项技能中的17项,而无基因缺失者则有25%的可能性掌握30项技能中的25项。总体而言,精细和粗大运动技能(如拿和够小东西、坐和在支持下行走)的掌握年龄范围较窄,而如厕、喂养和卫生技能的掌握年龄差异较大。与有基因缺失者(0-13%)相比,无基因缺失者实现独立如厕和穿衣等日常生活技能的概率更高(25-92%)。在所有分子亚型中,实现独立洗澡和刷牙的概率较低:结论:与有基因缺失的患者相比,无基因缺失的强直性脊柱炎患者更有可能较早达到发育里程碑和掌握日常生活技能。许多强直性脊柱炎患者无法掌握独立自理所需的日常生活技能。
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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.
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