The prevalence of autism in cerebellar malformations: a systematic review and meta-analysis.

IF 3.6 2区 医学 Q1 CLINICAL NEUROLOGY
Douglas A Wells, Danny Jaber, Shreya Dey, J Seth VanZant, Ross A Carson, Mary Lou Klem, Sima Sharghi, Ronald R Seese
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引用次数: 0

Abstract

The cerebellum contributes to the control of movement, language, and sociability. Purkinje cells, the main output neurons of the cerebellar cortex, are reduced in cerebellar malformations (CMs) and in autism spectrum disorder (ASD). Thus, CMs may increase the risk for ASD. We conducted a meta-analysis to determine the prevalence of ASD in individuals with CMs. We searched PubMed, Embase, and APA PsycINFO for studies assessing ASD in patients with radiologically confirmed CMs. We evaluated risk of bias using Joanna Briggs Institute Checklists. Finally, we extracted data to calculate ASD prevalence and assess variation across CM subtypes. From 1,564 screened articles, 32 studies met inclusion criteria, encompassing 1,032 individuals with CMs. ASD prevalence was 31.2%, significantly higher than the general population rate (1 in 31). High heterogeneity was observed (I² = 72.3%; p < 0.0001). Vermis and cerebellar hypoplasia reliably contributed to the high ASD prevalence. Many studies had small sample sizes and used different metrics to diagnose autism. ASD is more common in individuals with CMs, especially vermis malformations, than in the general population. Early neurodevelopmental monitoring may benefit those with prenatally diagnosed CMs.

自闭症在小脑畸形中的患病率:系统回顾和荟萃分析。
小脑负责控制运动、语言和社交能力。浦肯野细胞是小脑皮层的主要输出神经元,在小脑畸形(CMs)和自闭症谱系障碍(ASD)中减少。因此,CMs可能会增加患ASD的风险。我们进行了一项荟萃分析,以确定患有CMs的个体中ASD的患病率。我们检索了PubMed, Embase和APA PsycINFO,以评估放射学证实的CMs患者的ASD。我们使用乔安娜布里格斯研究所的检查表来评估偏倚风险。最后,我们提取数据来计算ASD患病率并评估CM亚型之间的差异。从1564篇筛选的文章中,32项研究符合纳入标准,包括1032名CMs患者。ASD患病率为31.2%,显著高于一般人群患病率(1 / 31)。观察到高度异质性(I²= 72.3%;p
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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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