Assessment of Adaptive Functioning and the Impact of Seizures in KBG Syndrome

IF 1.7 4区 生物学 Q3 GENETICS & HEREDITY American Journal of Medical Genetics Part A Pub Date : 2024-10-04 DOI:10.1002/ajmg.a.63896
Kathleen P. Sarino, Lily Guo, Edward Yi, Jiyeon Park, Ola Kierzkowska, Drake Carter, Elaine Marchi, Gholson J. Lyon
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Abstract

This study aimed to examine the adaptive functioning status and the impact of epileptic seizures on neurocognitive outcomes in KBG syndrome, a rare genetic neurodevelopmental disorder characterized by pathogenic variants in ANKRD11. A single clinician interviewed individuals and families with genetically confirmed cases of KBG syndrome. Trained professionals also conducted assessments using the Vineland–3 Adaptive Behavior Scales. The assessment covered the domains of communication, daily living skills, socialization, and maladaptive behaviors, and then compared individuals with and without epilepsy. Further comparisons were made with data from interviews and participants' medical records. Thirty-nine individuals (22 males, 17 females) with KBG syndrome, confirmed through genetic analysis, were interviewed via videoconferencing, followed by Vineland–3 assessment by trained raters. Individuals with KBG syndrome came from 36 unique families spanning 11 countries. While the KBG cohort displayed lower overall adaptive behavior composite scores compared with the average population, several members displayed standard scores at or higher than average, as well as higher scores compared with those with the neurodevelopmental disorder Ogden syndrome. Within the KBG cohort, males consistently scored lower than females across all domains, but none of these categories reached statistical significance. While the group with epilepsy exhibited overall lower scores than the nonseizure group in every category, statistical significance was only reached in the written communication subdomain. Our research provides insights that can aid in epilepsy screening and inform assessment strategies for neurocognitive functioning in those with this condition. The cohort performed overall higher than expected, with outliers existing in both directions. Although our results suggest that seizures might influence the trajectory of KBG syndrome, the approaching but overall absence of statistical significance between study groups underscores the need for a more extensive cohort to discern subtle variations in functioning.

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评估 KBG 综合征的适应功能和癫痫发作的影响。
KBG综合征是一种以ANKRD11致病变异为特征的罕见遗传性神经发育障碍,本研究旨在考察KBG综合征患者的适应功能状况以及癫痫发作对神经认知结果的影响。一名临床医生对经基因确诊的 KBG 综合征患者及其家庭进行了访谈。经过培训的专业人员还使用文兰-3 适应行为量表进行了评估。评估涵盖沟通、日常生活技能、社交和适应不良行为等领域,然后对患有癫痫和未患有癫痫的个体进行比较。通过访谈数据和参与者的医疗记录进行了进一步比较。经基因分析确认患有 KBG 综合征的 39 名患者(22 名男性,17 名女性)通过视频会议接受了访谈,随后由训练有素的评分员进行了维尼兰-3 评估。KBG 综合征患者来自 11 个国家的 36 个独特家庭。与普通人群相比,KBG 群体的总体适应行为综合得分较低,但有几名成员的标准分达到或高于平均水平,与神经发育障碍奥格登综合征患者相比,他们的得分也更高。在 KBG 群体中,男性在所有领域的得分一直低于女性,但这些类别均未达到统计学意义。虽然癫痫组在每个类别中的总分都低于非癫痫组,但只有在书面交流子域中达到了统计学意义。我们的研究提供了有助于癫痫筛查的见解,并为癫痫患者神经认知功能的评估策略提供了参考。组群的总体表现高于预期,但在两个方向上都存在异常值。虽然我们的研究结果表明癫痫发作可能会影响 KBG 综合征的发展轨迹,但研究组之间的接近性但总体上缺乏统计学意义,这突出表明需要更广泛的队列来辨别功能上的微妙变化。
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来源期刊
CiteScore
3.50
自引率
5.00%
发文量
432
审稿时长
2-4 weeks
期刊介绍: The American Journal of Medical Genetics - Part A (AJMG) gives you continuous coverage of all biological and medical aspects of genetic disorders and birth defects, as well as in-depth documentation of phenotype analysis within the current context of genotype/phenotype correlations. In addition to Part A , AJMG also publishes two other parts: Part B: Neuropsychiatric Genetics , covering experimental and clinical investigations of the genetic mechanisms underlying neurologic and psychiatric disorders. Part C: Seminars in Medical Genetics , guest-edited collections of thematic reviews of topical interest to the readership of AJMG .
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