Dataset Information

Autism Classification Using Topological Features and Deep Learning: A Cautionary Tale.

ABSTRACT: The identification of autistic individuals using resting state functional connectivity networks can provide an objective diagnostic method for autism spectrum disorder (ASD). The present state-of-the-art machine learning model using deep learning has a classification accuracy of 70.2% on the ABIDE (Autism Brain Imaging Data Exchange) data set. In this paper, we explore the utility of topological features in the classification of ASD versus typically developing control subjects. These topological features have been shown to provide a complementary source of discriminative information in applications such as 2D object classification and social network analysis. We evaluate the performance of three different representations of topological features - persistence diagrams, persistence images, and persistence landscapes - for autism classification using neural networks, support vector machines and random forests. We also propose a hybrid approach of augmenting topological features with functional correlations, which typically outperforms the models that use functional correlations alone. With this approach, even with a simple 3-layer neural network, we are able to achieve a classification accuracy of 69.2% on the ABIDE data set. However, our experiments also show that the improvement due to topological features is not always statistically significant. Therefore, we offer a cautionary tale to the practitioners regarding the limited discriminative power of topological features derived from fMRI data for the classification of autism.

SUBMITTER: Rathore A

PROVIDER: S-EPMC7390646 | biostudies-literature | 2019 Oct

REPOSITORIES: biostudies-literature

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Autism Classification Using Topological Features and Deep Learning: A Cautionary Tale.

Rathore Archit A Palande Sourabh S Anderson Jeffrey S JS Zielinski Brandon A BA Fletcher P Thomas PT Wang Bei B

Medical image computing and computer-assisted intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention 20191010

The identification of autistic individuals using resting state functional connectivity networks can provide an objective diagnostic method for autism spectrum disorder (ASD). The present state-of-the-art machine learning model using deep learning has a classification accuracy of 70.2% on the ABIDE (Autism Brain Imaging Data Exchange) data set. In this paper, we explore the utility of topological features in the classification of ASD versus typically developing control subjects. These topological ...[more]

PMID: 32728675

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Project description:Purpose: This study aimed to compare the performance of radiomics and deep learning in predicting EGFR mutation status in patients with lung cancer based on PET/CT images, and tried to explore a model with excellent prediction performance to accurately predict EGFR mutation status in patients with non-small cell lung cancer (NSCLC). Method: PET/CT images of 194 NSCLC patients from Xijing Hospital were collected and divided into a training set and a validation set according to the ratio of 7:3. Statistics were made on patients' clinical characteristics, and a large number of features were extracted based on their PET/CT images (4306 radiomics features and 2048 deep learning features per person) with the pyradiomics toolkit and 3D convolutional neural network. Then a radiomics model (RM), a deep learning model (DLM), and a hybrid model (HM) were established. The performance of the three models was compared by receiver operating characteristic (ROC) curves, sensitivity, specificity, accuracy, calibration curves, and decision curves. In addition, a nomogram based on a deep learning score (DS) and the most significant clinical characteristic was plotted. Result: In the training set composed of 138 patients (64 with EGFR mutation and 74 without EGFR mutation), the area under the ROC curve (AUC) of HM (0.91, 95% CI: 0.86-0.96) was higher than that of RM (0.82, 95% CI: 0.75-0.89) and DLM (0.90, 95% CI: 0.85-0.95). In the validation set composed of 57 patients (32 with EGFR mutation and 25 without EGFR mutation), the AUC of HM (0.85, 95% CI: 0.77-0.93) was also higher than that of RM (0.68, 95% CI: 0.52-0.84) and DLM (0.79, 95% CI: 0.67-0.91). In all, HM achieved better diagnostic performance in predicting EGFR mutation status in NSCLC patients than two other models. Conclusion: Our study showed that the deep learning model based on PET/CT images had better performance than radiomics model in diagnosing EGFR mutation status of NSCLC patients based on PET/CT images. Combined with the most statistically significant clinical characteristic (smoking) and deep learning features, our hybrid model had better performance in predicting EGFR mutation types of patients than two other models, which could enable NSCLC patients to choose more personalized treatment schemes.

Project description:BackgroundIn the United States, about 3 million people have autism spectrum disorder (ASD), and around 1 out of 59 children are diagnosed with ASD. People with ASD have characteristic social communication deficits and repetitive behaviors. The causes of this disorder remain unknown; however, in up to 25% of cases, a genetic cause can be identified. Detecting ASD as early as possible is desirable because early detection of ASD enables timely interventions in children with ASD. Identification of ASD based on objective pathogenic mutation screening is the major first step toward early intervention and effective treatment of affected children.ObjectiveRecent investigation interrogated genomics data for detecting and treating autism disorders, in addition to the conventional clinical interview as a diagnostic test. Since deep neural networks perform better than shallow machine learning models on complex and high-dimensional data, in this study, we sought to apply deep learning to genetic data obtained across thousands of simplex families at risk for ASD to identify contributory mutations and to create an advanced diagnostic classifier for autism screening.MethodsAfter preprocessing the genomics data from the Simons Simplex Collection, we extracted top ranking common variants that may be protective or pathogenic for autism based on a chi-square test. A convolutional neural network-based diagnostic classifier was then designed using the identified significant common variants to predict autism. The performance was then compared with shallow machine learning-based classifiers and randomly selected common variants.ResultsThe selected contributory common variants were significantly enriched in chromosome X while chromosome Y was also discriminatory in determining the identification of autistic individuals from nonautistic individuals. The ARSD, MAGEB16, and MXRA5 genes had the largest effect in the contributory variants. Thus, screening algorithms were adapted to include these common variants. The deep learning model yielded an area under the receiver operating characteristic curve of 0.955 and an accuracy of 88% for identifying autistic individuals from nonautistic individuals. Our classifier demonstrated a considerable improvement of ~13% in terms of classification accuracy compared to standard autism screening tools.ConclusionsCommon variants are informative for autism identification. Our findings also suggest that the deep learning process is a reliable method for distinguishing the diseased group from the control group based on the common variants of autism.

Dataset Information

Autism Classification Using Topological Features and Deep Learning: A Cautionary Tale.

Publications

Autism Classification Using Topological Features and Deep Learning: A Cautionary Tale.

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