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探索自闭症中重复刻板行为和兴趣(RRBI)的多维性质:神经解剖学相关性及临床意义。

Exploring the multidimensional nature of repetitive and restricted behaviors and interests (RRBI) in autism: neuroanatomical correlates and clinical implications.

机构信息

Fondation Vallée, GHT Paris Sud, Hospital of Child and Adolescent Psychiatry, Gentilly, France.

UMR 3571 CNRS, Human Genetics and Cognitive Functions, Institut Pasteur, Paris, France.

出版信息

Mol Autism. 2023 Nov 27;14(1):45. doi: 10.1186/s13229-023-00576-z.

DOI:10.1186/s13229-023-00576-z
PMID:38012709
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10680239/
Abstract

BACKGROUND

Repetitive and restricted behaviors and interests (RRBI) are core symptoms of autism with a complex entity and are commonly categorized into 'motor-driven' and 'cognitively driven'. RRBI symptomatology depends on the individual's clinical environment limiting the understanding of RRBI physiology, particularly their associated neuroanatomical structures. The complex RRBI heterogeneity needs to explore the whole RRBI spectrum by integrating the clinical context [autistic individuals, their relatives and typical developing (TD) individuals]. We hypothesized that different RRBI dimensions would emerge by exploring the whole spectrum of RRBI and that these dimensions are associated with neuroanatomical signatures-involving cortical and subcortical areas.

METHOD

A sample of 792 individuals composed of 267 autistic subjects, their 370 first-degree relatives and 155 TD individuals was enrolled in the study. We assessed the whole patterns of RRBI in each individual by using the Repetitive Behavior Scale-Revised and the Yale-Brown Obsessive Compulsive Scale. We estimated brain volumes using MRI scanner for a subsample of the subjects (n = 152, 42 ASD, 89 relatives and 13 TD). We first investigated the dimensionality of RRBI by performing a principal component analysis on all items of these scales and included all the sampling population. We then explored the relationship between RRBI-derived factors with brain volumes using linear regression models.

RESULTS

We identified 3 main factors (with 30.3% of the RRBI cumulative variance): Factor 1 (FA1, 12.7%) reflected mainly the 'motor-driven' RRBI symptoms; Factor 2 and 3 (respectively, 8.8% and 7.9%) gathered mainly Y-BOCS related items and represented the 'cognitively driven' RRBI symptoms. These three factors were significantly associated with the right/left putamen volumes but with opposite effects: FA1 was negatively associated with an increased volume of the right/left putamen conversely to FA2 and FA3 (all uncorrected p < 0.05). FA1 was negatively associated with the left amygdala (uncorrected p < 0.05), and FA2 was positively associated with the left parietal structure (uncorrected p = 0.001).

CONCLUSION

Our results suggested 3 coherent RRBI dimensions involving the putamen commonly and other structures according to the RRBI dimension. The exploration of the putamen's integrative role in RSBI needs to be strengthened in further studies.

摘要

背景

重复和受限的行为和兴趣(RRBI)是自闭症的核心症状,具有复杂的实体,通常分为“运动驱动”和“认知驱动”。RRBI 的症状取决于个体的临床环境,这限制了对 RRBI 生理学的理解,特别是对其相关神经解剖结构的理解。复杂的 RRBI 异质性需要通过整合临床环境[自闭症个体、他们的亲属和典型发育(TD)个体]来探索整个 RRBI 谱来探索。我们假设通过探索整个 RRBI 谱,会出现不同的 RRBI 维度,并且这些维度与涉及皮质和皮质下区域的神经解剖特征相关。

方法

本研究纳入了 792 名个体,包括 267 名自闭症患者、他们的 370 名一级亲属和 155 名 TD 个体。我们使用重复性行为量表修订版和耶鲁-布朗强迫症量表评估了每个个体的整个 RRBI 模式。我们使用 MRI 扫描仪对受试者的亚样本(n=152,42 名 ASD、89 名亲属和 13 名 TD)进行了脑容量估计。我们首先对这些量表的所有项目进行主成分分析,以探索 RRBI 的维度,并包括所有抽样人群。然后,我们使用线性回归模型探索了 RRBI 衍生因素与脑容量之间的关系。

结果

我们确定了 3 个主要因素(占 RRBI 累积方差的 30.3%):第 1 因子(FA1,占 12.7%)主要反映了“运动驱动”RRBI 症状;第 2 因子和第 3 因子(分别为 8.8%和 7.9%)主要汇集了与 Y-BOCS 相关的项目,代表了“认知驱动”RRBI 症状。这三个因素与右侧/左侧壳核体积显著相关,但作用相反:FA1 与右侧/左侧壳核体积的增加呈负相关,而 FA2 和 FA3 则呈正相关(所有未校正的 p<0.05)。FA1 与左侧杏仁核呈负相关(未校正的 p<0.05),FA2 与左侧顶叶结构呈正相关(未校正的 p=0.001)。

结论

我们的研究结果表明,有 3 个连贯的 RRBI 维度涉及壳核,通常还涉及根据 RRBI 维度的其他结构。需要在进一步的研究中加强对壳核在 RRBI 中的整合作用的探索。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97b8/10680239/6668a78d1a3c/13229_2023_576_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97b8/10680239/6668a78d1a3c/13229_2023_576_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/97b8/10680239/6668a78d1a3c/13229_2023_576_Fig1_HTML.jpg

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