Lala Maria Rosaria, Bellantoni Domenica, Montanaro Federica Alice Maria, Pontillo Maria, Alfieri Paolo, Vicari Stefano
Department of Life Sciences and Public Health, Università Cattolica Del Sacro Cuore, Rome, Italy.
Child & Adolescent Neuropsychiatry Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Front Psychiatry. 2025 Jul 23;16:1595492. doi: 10.3389/fpsyt.2025.1595492. eCollection 2025.
22q11.2 deletion syndrome (22q11.2DS), also known as velo-cardiofacial syndrome or DiGeorge syndrome (DGS) is highly variable in phenotype, encompassing a wide range of physical and neuropsychiatric manifestations (ID, ADHD, ASD, anxiety, major depressive disorder,obsessive-compulsive disorder, schizophrenia). In this retrospective study, we aimed to assess the clinical significance of sleep disturbances and their relationship with functional impairment in a cohort of 52 children and adolescents with 22q11.2DS, as well as psychological distress in their parents. Standardized measures, including the Sleep Disturbance Scale for Children (SDSC) and the Parenting Stress Index-Short Form (PSI-SF), were administered to parents.
The sample consisted of 26 males and 26 females, aged 5 to 18 years. Participants were referred to the Day Hospital follow up of Child and Adolescent Neuropsychiatry Unit in the Bambino Gesù Children's Hospital in Rome, Italy, between January 2023 and December 2023. The total cohort was divided into two main groups based on the presence of sleep problems: (1) Group 1, with sleep problems, and (2) Group 2, without sleep problems. Both groups demonstrated low mean IQ scores and low general adaptive functioning, as measured by the Wechsler Intelligence Scale for Children (WISC-IV) and the ABAS II General Adaptive Composite (GAC), respectively. Furthermore, Group 1 exhibited significantly lower functioning when assessed using the CGAS. Additionally, Group 1 reported higher levels of self-reported anxiety symptoms (MASC-2) compared to Group 2. While none of the results reached the clinical range, scores in Group 1 were generally higher, particularly on the "Performance Fears" subscale. A similar trend was observed in the "Negative Self-Esteem" subtest of the CDI 2 (self-report form). Although the average questionnaire scores did not fall within the clinical range, KSADS psychiatric diagnoses revealed the presence of various psychiatric disorders. Unexpectedly, these disorders were more prevalent in the group without sleep problems, except for anxiety disorders, which showed similar prevalence across both groups. Regarding parental stress, as measured by the PSI-SF, we did not observe a significant relationship between sleep disorders and parental stress, on the contrary to our expectations.
Our study is one of the few to specifically investigate sleep problems in the pediatric population with 22q11.2DS and the first to use the Sleep Disturbance Scale for Children (SDSC) to assess various aspects of sleep disorders in this group. Further studies are required to draw more consistent conclusions.
22q11.2缺失综合征(22q11.2DS),也称为心脏颜面综合征或迪格奥尔格综合征(DGS),其表型具有高度变异性,涵盖广泛的身体和神经精神表现(智力缺陷、注意力缺陷多动障碍、自闭症谱系障碍、焦虑症、重度抑郁症、强迫症、精神分裂症)。在这项回顾性研究中,我们旨在评估52名患有22q11.2DS的儿童和青少年队列中睡眠障碍的临床意义及其与功能损害的关系,以及他们父母的心理困扰。我们向父母发放了标准化测量工具,包括儿童睡眠障碍量表(SDSC)和父母压力指数简表(PSI-SF)。
样本包括26名男性和26名女性,年龄在5至18岁之间。参与者于2023年1月至2023年12月期间被转介至意大利罗马的圣心儿童医院儿童和青少年神经精神病科日间医院进行随访。根据是否存在睡眠问题,将整个队列分为两个主要组:(1)第1组,有睡眠问题;(2)第2组,无睡眠问题。两组的平均智商得分均较低,总体适应功能也较低,分别通过韦氏儿童智力量表(WISC-IV)和ABAS II总体适应综合量表(GAC)进行测量。此外,使用儿童总体评估量表(CGAS)评估时,第1组的功能明显更低。此外,与第2组相比,第1组自我报告的焦虑症状水平(MASC-2)更高。虽然没有任何结果达到临床范围,但第1组的得分总体上更高,尤其是在 “表现恐惧” 子量表上。在儿童抑郁量表第二版(自我报告表)的 “消极自尊” 子测试中也观察到了类似趋势。尽管问卷平均得分未落在临床范围内,但KSADS精神科诊断显示存在各种精神障碍。出乎意料的是,除焦虑症在两组中的患病率相似外,这些障碍在无睡眠问题的组中更为普遍。关于通过PSI-SF测量的父母压力,与我们的预期相反,我们没有观察到睡眠障碍与父母压力之间存在显著关系。
我们的研究是少数专门调查患有22q11.2DS的儿科人群睡眠问题的研究之一,也是首个使用儿童睡眠障碍量表(SDSC)评估该组睡眠障碍各个方面的研究。需要进一步的研究来得出更一致的结论。