scholarly journals Behavioural profiling of autism connectivity abnormalities

BJPsych Open ◽  
2020 ◽  
Vol 6 (1) ◽  
Author(s):  
William Snyder ◽  
Vanessa Troiani

Background Brain regions are functionally diverse, and a given region may engage in a variety of tasks. This functional diversity of brain regions may be one factor that has prevented the finding of consistent biomarkers for brain disorders such as autism spectrum disorder (ASD). Thus, methods to characterise brain regions would help to determine how functional abnormalities contribute to affected behaviours. Aims As the first illustration of the meta-analytic behavioural profiling procedure, we evaluated how the regions with disrupted connectivity in ASD contributed to various behaviours. Method Connectivity abnormalities were determined from a published degree centrality group comparison based on functional magnetic resonance imaging data from the Autism Brain Imaging Data Exchange. Using BrainMap's database of task-based neuroimaging studies, behavioural profiles were created for abnormally connected regions by relating these regions to tasks activating them. Results Hyperconnectivity in ASD brains was significantly related to memory, attention, reasoning, social, execution and speech behaviours. Hypoconnectivity was related to vision, execution and speech behaviours. Conclusions The procedure outlines the first clinical neuroimaging application of a behavioural profiling method that estimates the functional diversity of brain regions, allowing for the relation of abnormal functional connectivity to diagnostic criteria. Behavioural profiling and the computational insights it provides can facilitate better understanding of the functional manifestations of various disorders, including ASD.

2021 ◽  
Author(s):  
Fatima zahra Benabdallah ◽  
Ahmed Drissi El Maliani ◽  
Dounia Lotfi ◽  
Rachid Jennane ◽  
Mohammed El hassouni

Abstract Autism spectrum disorder (ASD) is theoretically characterized by alterations in functional connectivity between brain regions. Many works presented approaches to determine informative patterns that help to predict autism from typical development. However, most of the proposed pipelines are not specifically designed for the autism problem, i.e they do not corroborate with autism theories about functional connectivity. In this paper, we propose a framework that takes into account the properties of local connectivity and long range under-connectivity in the autistic brain. The originality of the proposed approach is to adopt elimination as a technique in order to well emerge the autistic brain connectivity alterations, and show how they contribute to differentiate ASD from controls. Experimental results conducted on the large multi-site Autism Brain Imaging Data Exchange (ABIDE) show that our approach provides accurate prediction up to 70% and succeeds to prove the existence of deficits in the long-range connectivity in the ASD subjects brains.


2016 ◽  
Author(s):  
Xin Di ◽  
Bharat B Biswal

Background: Males are more likely to suffer from autism spectrum disorder (ASD) than females. As to whether females with ASD have similar brain alterations remain an open question. The current study aimed to examine sex-dependent as well as sex-independent alterations in resting-state functional connectivity in individuals with ASD compared with typically developing (TD) individuals. Method: Resting-state functional MRI data were acquired from the Autism Brain Imaging Data Exchange (ABIDE). Subjects between 6 to 20 years of age were included for analysis. After matching the intelligence quotient between groups for each dataset, and removing subjects due to excessive head motion, the resulting effective sample contained 28 females with ASD, 49 TD females, 129 males with ASD, and 141 TD males, with a two (diagnosis) by two (sex) design. Functional connectivity among 153 regions of interest (ROIs) comprising the whole brain was computed. Two by two analysis of variance was used to identify connectivity that showed diagnosis by sex interaction or main effects of diagnosis. Results: The main effects of diagnosis were found mainly between visual cortex and other brain regions, indicating sex-independent connectivity alterations. We also observed two connections whose connectivity showed diagnosis by sex interaction between the precuneus and medial cerebellum as well as the precunes and dorsal frontal cortex. While males with ASD showed higher connectivity in these connections compared with TD males, females with ASD had lower connectivity than their counterparts. Conclusions: Both sex-dependent and sex-independent functional connectivity alterations are present in ASD.


2019 ◽  
Author(s):  
Yafeng Zhan ◽  
Jianze Wei ◽  
Jian Liang ◽  
Xiu Xu ◽  
Ran He ◽  
...  

AbstractPsychiatric disorders often exhibit shared (co-morbid) symptoms, raising controversies over accurate diagnosis and the overlap of their neural underpinnings. Because the complexity of data generated by clinical studies poses a formidable challenge, we have pursued a reductionist framework using brain imaging data of a transgenic primate model of autism spectrum disorder (ASD). Here we report an interpretable cross-species machine learning approach which extracts transgene-related core regions in the monkey brain to construct the classifier for diagnostic classification in humans. The cross-species classifier based on core regions, mainly distributed in frontal and temporal cortex, identified from the transgenic primate model, achieved an accuracy of 82.14% in one clinical ASD cohort obtained from Autism Brain Imaging Data Exchange (ABIDE-I), significantly higher than the human-based classifier (61.31%, p < 0.001), which was validated in another independent ASD cohort obtained from ABIDE-II. Such monkey-based classifier generalized to achieve a better classification in obsessive-compulsive disorder (OCD) cohorts, and enabled parsing of differential connections to right ventrolateral prefrontal cortex being attributable to distinct traits in patients with ASD and OCD. These findings underscore the importance of investigating biologically homogeneous samples, particularly in the absence of real-world data adequate for deconstructing heterogeneity inherited in the clinical cohorts.One Sentence SummaryFeatures learned from transgenic monkeys enable improved diagnosis of autism-related disorders and dissection of their underlying circuits.


2019 ◽  
Author(s):  
Marion Fouquet ◽  
Nicolas Traut ◽  
Anita Beggiato ◽  
Richard Delorme ◽  
Thomas Bourgeron ◽  
...  

AbstractThe contrast of the interface between the neocortical grey matter and the white matter is emerging as an important neuroimaging phenotype for several brain disorders. To date, a single in vivo study has analysed the cortical grey-to-white matter percent contrast (GWPC) on Magnetic Resonance Imaging (MRI), and has shown a significant decrease of this contrast in several areas in individuals with Autism Spectrum Disorder (ASD). Our goal was to replicate this study across a larger cohort, using the multicenter data from the Autism Brain Imaging Data Exchange 1 and 2 gathering data from 2,148 subjects. Multiple linear regression was used to study the effect of the diagnosis of ASD on the GWPC. Contrary to the first study, we found a statistically significant increase of GWPC among individuals with ASD in left auditory and bilateral visual sensory areas, as well as in the left primary motor cortex. These results were still statistically significant after inclusion of cortical thickness as covariate. There are numerous reports of sensory-motor atypicalities in patients with ASD, which may be the reason for the differences in GWPC that we observed. Further investigation could help us determine the potential role of a defect or a delay in intra-cortical myelination of sensory-motor regions in ASD. Code: https://github.com/neuroanatomy/GWPC.


2017 ◽  
Author(s):  
Nicolas Traut ◽  
Anita Beggiato ◽  
Thomas Bourgeron ◽  
Richard Delorme ◽  
Laure Rondi-Reig ◽  
...  

AbstractCerebellar volume abnormalities have been often suggested as a possible endophenotype for autism spectrum disorder (ASD). We aimed at objectifying this possible alteration by performing a systematic meta-analysis of the literature, and an analysis of the Autism Brain Imaging Data Exchange (ABIDE) cohort. Our meta-analysis sought to determine a combined effect size of ASD diagnosis on different measures of the cerebellar anatomy, as well as the effect of possible factors of variability across studies. We then analysed the cerebellar volume of 328 patients and 353 controls from the ABIDE project. The meta-analysis of the literature suggested a weak but significant association between ASD diagnosis and increased cerebellar volume (p=0.049, uncorrected), but the analysis of ABIDE did not show any relationship. The studies in the literature were generally underpowered, however, the number of statistically significant findings was larger than expected. Although we could not provide a conclusive explanation for this excess of significant findings, our analyses would suggest publication bias as a possible reason. Finally, age, sex and IQ were important sources of cerebellar volume variability, however, independent of autism diagnosis.


2021 ◽  
Vol 83 (3) ◽  
pp. 45-52
Author(s):  
R. Nur Syahindah Husna ◽  
A. R. Syafeeza ◽  
Norihan Abdul Hamid ◽  
Y. C. Wong ◽  
R. Atikah Raihan

Autism Spectrum Disorders (ASDs) define as a scope of disability in the development of certain conditions such as social communication, imagination, and patients' capabilities to make some connection. In Malaysia, the number of ASD cases diagnosed is increasing each year. Typically, ASD patients are analyzed by doctors based on history and behavior observation without the ability to diagnose instantaneously. This research intends to study the ASD biomarker based on neuroimaging functional Magnetic Resonance Imaging (fMRI) images, which can aid doctors in diagnosing ASD. This study applies a deep learning method from Convolutional Neural Network (CNN) variants to detect either the patients are ASD or non-ASD and extract the robust characteristics from neuroimages in fMRI. Then, it interprets the performance of pre-processed images in the form of accuracy to classify the neural patterns. The Autism Brain Imaging Data Exchange (ABIDE) dataset was used to research the brain imaging of ASD patients. The results achieved using CNN models namely VGG-16 and ResNet-50 are 63.4% and 87.0% accuracy, respectively. This method also assists doctors in detecting Autism from a quantifiable method that is not dependent on the behavioral observations of suspected autistic children.


Diagnostics ◽  
2022 ◽  
Vol 12 (1) ◽  
pp. 165
Author(s):  
Mohamed T. Ali ◽  
Yaser ElNakieb ◽  
Ahmed Elnakib ◽  
Ahmed Shalaby ◽  
Ali Mahmoud ◽  
...  

This study proposes a Computer-Aided Diagnostic (CAD) system to diagnose subjects with autism spectrum disorder (ASD). The CAD system identifies morphological anomalies within the brain regions of ASD subjects. Cortical features are scored according to their contribution in diagnosing a subject to be ASD or typically developed (TD) based on a trained machine-learning (ML) model. This approach opens the hope for developing a new CAD system for early personalized diagnosis of ASD. We propose a framework to extract the cerebral cortex from structural MRI as well as identifying the altered areas in the cerebral cortex. This framework consists of the following five main steps: (i) extraction of cerebral cortex from structural MRI; (ii) cortical parcellation to a standard atlas; (iii) identifying ASD associated cortical markers; (iv) adjusting feature values according to sex and age; (v) building tailored neuro-atlases to identify ASD; and (vi) artificial neural networks (NN) are trained to classify ASD. The system is tested on the Autism Brain Imaging Data Exchange (ABIDE I) sites achieving an average balanced accuracy score of 97±2%. This paper demonstrates the ability to develop an objective CAD system using structure MRI and tailored neuro-atlases describing specific developmental patterns of the brain in autism.


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