Clinical, genetic, and cognitive correlates of seizure occurrences in Phelan-McDermid syndrome.

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY
Tess Levy, Jacob Gluckman, Paige M Siper, Danielle Halpern, Jessica Zweifach, Rajna Filip-Dhima, J Lloyd Holder, M Pilar Trelles, Kristina Johnson, Jonathan A Bernstein, Elizabeth Berry-Kravis, Craig M Powell, Latha Valluripalli Soorya, Audrey Thurm, Joseph D Buxbaum, Mustafa Sahin, Alexander Kolevzon, Siddharth Srivastava
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引用次数: 0

Abstract

Background: Phelan-McDermid syndrome (PMS) is a genetic neurodevelopmental disorder caused by SHANK3 haploinsufficiency and is associated with an increased risk for seizures. Previous literature indicates that around one third of individuals with PMS also have epilepsy or seizures, with a wide range of types and ages of onset. Investigating the impact of seizures on intellectual and adaptive functioning for PMS is a primary concern for caregivers and is important to understanding the natural history of this syndrome.

Methods: We report on results from 98 individuals enrolled in a prospective, longitudinal study. We detailed seizure frequency, type, and age of onset, and we analyzed seizure occurrence with best estimate IQ, adaptive functioning, clinical features, and genotype. We conducted multiple linear regression analyses to assess the relationship between the presence of seizures and the Vineland Adaptive Behavior Scale, Second Edition (VABS-II) Adaptive Behavior Composite score and the best estimate full-scale IQ. We also performed Chi-square tests to explore associations between seizure prevalence and genetic groupings. Finally, we performed Chi-square tests and t-tests to explore the relationship between seizures and demographic features, features that manifest in infancy, and medical features.

Results: Seizures were present in 41% of the cohort, and age of onset was widely variable. The presence of seizures was associated with significantly lower adaptive and intellectual functioning. Genotype-phenotype analyses were discrepant, with no differences in seizure prevalence across genetic classes, but with more genes included in deletions of participants with 22q13 deletions and seizures compared to those with 22q13 deletions and no seizures. No clinical associations were found between the presence of seizures and sex, history of pre- or neonatal complications, early infancy, or medical features. In this cohort, generalized seizures were associated with developmental regression, which is a top concern for PMS caregivers.

Conclusions: These results begin to eludicate correlates of seizures in individuals with PMS and highlight the importance of early seizure management. Importantly, presence of seizures was associated with adaptive and cognitive functioning. A larger cohort might be able to identify additional associations with medical features. Genetic findings suggest an increased capability to realize genotype-phenotype relationships when deletion size is taken into account.

佩兰-麦克德米综合征癫痫发作的临床、遗传和认知相关性。
背景:菲兰-麦克德米综合征(PMS)是一种由 SHANK3 单倍体缺乏引起的遗传性神经发育障碍,与癫痫发作风险增加有关。以往的文献表明,约有三分之一的 PMS 患者同时患有癫痫或癫痫发作,类型和发病年龄各不相同。调查癫痫发作对 PMS 患者智力和适应功能的影响是护理人员最关心的问题,对于了解该综合征的自然史也非常重要:我们报告了一项前瞻性纵向研究中 98 名患者的研究结果。我们详细介绍了癫痫发作频率、类型和发病年龄,并分析了癫痫发作与最佳估计智商、适应功能、临床特征和基因型的关系。我们进行了多元线性回归分析,以评估癫痫发作与维尼兰适应行为量表第二版(VABS-II)适应行为综合评分和最佳估计全面智商之间的关系。我们还进行了卡方检验,以探讨癫痫发作率与遗传分组之间的关联。最后,我们进行了卡方检验和 t 检验,以探讨癫痫发作与人口统计学特征、婴儿期表现特征和医学特征之间的关系:结果:41%的患者有癫痫发作,发病年龄差异很大。癫痫发作与较低的适应能力和智力相关。基因型-表型分析结果显示,不同基因类别的癫痫发作率没有差异,但与22q13缺失且无癫痫发作的患者相比,22q13缺失且有癫痫发作的患者的基因缺失率更高。没有发现癫痫发作与性别、产前或新生儿并发症病史、婴儿早期或医学特征有临床关联。在这个队列中,全身性癫痫发作与发育倒退有关,而发育倒退是早产儿护理人员最关心的问题:这些结果开始阐明 PMS 患者癫痫发作的相关性,并强调了早期癫痫发作管理的重要性。重要的是,癫痫发作与适应能力和认知功能相关。更大规模的队列可能会发现与医疗特征的其他关联。遗传学研究结果表明,如果考虑到基因缺失的大小,实现基因型与表型关系的能力就会提高。
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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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