Department of Psychiatry, Rudolf Magnus Institute of Neuroscience, University Medical Center Utrecht, Utrecht, The Netherlands.
Dalglish Family 22q Clinic for Adults with 22q11.2 Deletion Syndrome, Toronto General Hospital, University Health Network, and Clinical Genetics Research Program, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
Am J Med Genet A. 2018 Oct;176(10):2182-2191. doi: 10.1002/ajmg.a.40387. Epub 2018 Sep 8.
The purpose of this article is to provide an overview of current insights into the neurodevelopmental and psychiatric manifestations of 22q11.2 deletion syndrome (22q11DS) in children and adolescents. The pediatric neuropsychiatric expression of 22q11DS is characterized by high variability, both interindividual and intraindividual (different expressions over the lifespan). Besides varying levels of intellectual disability, the prevalence of autism spectrum disorders, attention deficit disorders, anxiety disorders, and psychotic disorders in young individuals with 22q11DS is significantly higher than in the general population, or in individuals with idiopathic intellectual disability. Possible explanations for this observed phenotypic variability will be discussed, including genetic pleiotropy, gene-environment interactions, the age-dependency of phenotypes, but also the impact of assessment and ascertainment bias as well as the limitations of our current diagnostic classification system. The implications inferred by these observations aforementioned bear direct relevance to both scientists and clinicians. Observations regarding the neuropsychiatric manifestations in individuals with 22q11DS exemplify the need for a dimensional approach to neuropsychiatric assessment, in addition to our current categorical diagnostic classification system. The potential usefulness of 22q11DS as a genetic model to study the early phases of schizophrenia as well as the phenomenon of neuropsychiatric pleiotropy observed in many CNV's will be delineated. From a clinical perspective, the importance of regular neuropsychiatric evaluations with attention to symptoms not always captured in diagnostic categories and of maintaining equilibrium between individual difficulties and competencies and environmental demands will be discussed.
本文旨在概述儿童和青少年时期 22q11.2 缺失综合征(22q11DS)的神经发育和精神表现的最新认识。22q11DS 的儿科神经精神表现具有高度的个体间和个体内变异性(个体在其一生中的不同表现)。除了不同程度的智力残疾外,22q11DS 个体中自闭症谱系障碍、注意力缺陷障碍、焦虑障碍和精神病障碍的患病率明显高于普通人群或特发性智力残疾个体。将讨论这种观察到的表型变异性的可能解释,包括遗传多效性、基因-环境相互作用、表型的年龄依赖性,但也包括评估和确定偏倚以及我们当前诊断分类系统的局限性。这些观察结果对科学家和临床医生都有直接的意义。22q11DS 个体的神经精神表现观察结果例证了需要对神经精神评估采用维度方法,而不仅仅是我们目前的分类诊断系统。22q11DS 作为研究精神分裂症早期阶段以及许多 CNV 中观察到的神经精神多效性现象的遗传模型的潜在用途将被描述。从临床角度来看,需要定期进行神经精神评估,注意诊断类别中未捕获的症状,并在个体困难和能力与环境需求之间保持平衡,这一点非常重要。