Frattale Ilaria, Sarnataro Rachele, Siracusano Martina, Riccioni Assia, Galasso Cinzia, Valeriani Massimiliano, Conteduca Giuseppina, Coviello Domenico, Mazzone Luigi, Moavero Romina
Child Neurology and Psychiatry Unit, Department of Wellbeing of Mental and Neurological, Dental and Sensory Organ Health, Policlinico Tor Vergata Foundation Hospital, Rome, Italy.
Department of Biomedicine and Prevention, University of Rome Tor Vergata, Rome, Italy.
Front Neurol. 2024 Feb 16;15:1360055. doi: 10.3389/fneur.2024.1360055. eCollection 2024.
Sotos syndrome (SoS) is a rare overgrowth genetic disease caused by intragenic mutations or microdeletions of the gene located on chromosome 5q35. SoS population might present cognitive impairment and a spectrum of behavioral characteristics, with a worse profile in patients with microdeletion. Although patients with SoS are known to have impaired sleep habits, very little data are available. The present study aimed to assess the prevalence of sleep disorders (SDs) in a pediatric cohort of patients with SoS and their correlation with neuropsychiatric profiles.
We included patients with a SoS diagnosis and age < 18 years; all patients underwent a comprehensive neuropsychological assessment, including evaluation of cognition, adaptive functions through the Adaptive Behavior Assessment System-Second Edition (ABAS-II), and behavioral problems using the Achenbach Child Behavior Checklist (CBCL) and Conners' Parent Rating Scale-Revised (CPRS-R:L) questionnaire. To investigate the presence of SD parents, the Sleep Disturbance Scale for Children (SDSC) was completed.
Thirty-eight patients (M 61%, F 39%, mean age 11.1 ± 4.65 years) were included in the study. Although only two had a prior SD diagnosis, 71.1% (N = 27) exhibited pathological scores on SDSC. No statistically significant associations were found between positive SDSC results and genetic microdeletion, intellectual disability (ID), or other medical conditions/treatments. However, a positive correlation emerged between SDSC scores and Conners' Global Index ( = 0.048) and Restless/Impulsive ( = 0.01) scores, CBCL externalizing ( = 0.02), internalizing (p = 0.01), and total scores ( = 0.05). Conversely, a negative linear relationship was observed between the SDSC score and the ABAS GAC and ABAS CAD scores ( = 0.025).
We detected an SD in 71.1% of our sample, with a positive relation between SD and internalizing and externalizing symptom levels, especially hyperactivity and impulsivity. Our study demonstrated a high prevalence of SD in pediatric patients with SoS, highlighting that all patients should be screened for this problem, which has a great impact on the quality of life of patients and their families.
索托斯综合征(SoS)是一种罕见的过度生长遗传性疾病,由位于5号染色体q35区域的基因发生基因内突变或微缺失引起。索托斯综合征患者可能存在认知障碍和一系列行为特征,微缺失患者的情况更严重。尽管已知索托斯综合征患者存在睡眠习惯受损的情况,但相关数据非常少。本研究旨在评估索托斯综合征儿科患者队列中睡眠障碍(SDs)的患病率及其与神经精神特征的相关性。
我们纳入了诊断为索托斯综合征且年龄<18岁的患者;所有患者均接受了全面的神经心理学评估,包括认知评估、通过《适应性行为评估系统第二版》(ABAS-II)评估适应性功能,以及使用阿肯巴克儿童行为清单(CBCL)和康纳斯父母评定量表修订版(CPRS-R:L)问卷评估行为问题。为调查患者父母是否存在睡眠障碍,完成了儿童睡眠障碍量表(SDSC)。
本研究纳入了38例患者(男性占61%,女性占39%,平均年龄11.1±4.65岁)。尽管只有2例之前被诊断为睡眠障碍,但71.1%(N = 27)的患者在SDSC上表现出病理评分。SDSC阳性结果与基因微缺失、智力残疾(ID)或其他医疗状况/治疗之间未发现统计学上的显著关联。然而,SDSC评分与康纳斯综合指数(r = 0.048)、多动/冲动(r = 0.01)评分、CBCL外化(r = 0.02)、内化(p = 0.01)及总分(r = 0.05)之间呈正相关。相反,观察到SDSC评分与ABAS GAC和ABAS CAD评分之间呈负线性关系(r = 0.025)。
我们在71.1%的样本中检测到睡眠障碍,睡眠障碍与内化和外化症状水平呈正相关,尤其是多动和冲动。我们的研究表明,索托斯综合征儿科患者中睡眠障碍的患病率很高,强调应对所有患者进行该问题的筛查,因为这对患者及其家庭的生活质量有很大影响。