Alzheimer’s Disease Computer-Aided Diagnosis on Positron Emission Tomography Brain Images Using Image Processing Techniques

Positron emission tomography (PET) is a molecular medical imaging modality which is commonly used for neurodegenerative disease diagnosis. Computer-aided diagnosis (CAD), based on medical image analysis, could help with the quantitative evaluation of brain diseases such as Alzheimer’s disease (AD). Ranking the effectiveness of brain volume of interest (VOI) to separate healthy or normal control (HC or NC) from AD brain PET images is presented in this book chapter. Brain images are first mapped into anatomical VOIs using an atlas. Different features including statistical, graph, or connectivity-based features are then computed on these VOIs. Top-ranked VOIs are then input into a support vector machine (SVM) classifier. The developed methods are evaluated on a local database image as well as on Alzheimer’s Disease Neuroimaging Initiative (ADNI) public database and then compared to known selection feature methods. These new approaches outperformed classification results in the case of a two-group separation

Brain Region Ranking for 18FDG-PET Computer-Aided Diagnosis of Alzheimer’s Disease

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Region-based brain selection and classification on pet images for Alzheimer disease computer aided diagnosis

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A novel feature selection in the case of brain pet image classification

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REHABILITATION DEVICES AND SYSTEMS Histogram-Based Features Selection and Volume of Interest Ranking for Brain PET Image Classification

International audiencePositron emission tomography (PET) is a molecular medical imaging modality which is commonly used for neurodegenerative diseases diagnosis. Computer-aided diagnosis, based on medical image analysis, could help quantitative evaluation of brain diseases such as Alzheimer's disease (AD). A novel method of ranking the effectiveness of brain volume of interest (VOI) to separate healthy control from AD brains PET images is presented in this paper. Brain images are first mapped into anatomical VOIs using an atlas. Histogram-based features are then extracted and used to select and rank VOIs according to the area under curve (AUC) parameter, which produces a hierarchy of the ability of VOIs to separate between groups of subjects. The top-ranked VOIs are then input into a support vector machine classifier. The developed method is evaluated on a local database image and compared to the known selection feature methods. Results show that using AUC outperforms classification results in the case of a two group separation

Region of interest selection using statistical parameters on brain 18FDG Positron Emission Tomography images

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Brain Region of Interest Selection for 18FDG Positrons Emission Tomography Computer-aided Image Classification

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Improvements and inter-laboratory implementation and optimization of blood-based single-locus age prediction models using DNA methylation of the ELOVL2 promoter

International audienceSeveral blood-based age prediction models have been developed using less than a dozen to more than a hundred DNA methylation biomarkers. Only one model (Z-P1) based on pyrosequencing has been developed using DNA methylation of a single locus located in the ELOVL2 promoter, which is considered as one of the best age-prediction biomarker. Although multi-locus models generally present better performances compared to the single-locus model, they require more DNA and present more inter-laboratory variations impacting the predictions. Here we developed 17,018 single-locus age prediction models based on DNA methylation of the ELOVL2 promoter from pooled data of four different studies (training set of 1,028 individuals aged from 0 and 91 years) using six different statistical approaches and testing every combination of the 7 CpGs, aiming to improve the prediction performances and reduce the effects of inter-laboratory variations. Compared to Z-P1 model, three statistical models with the optimal combinations of CpGs presented improved performances (MAD of 4.41–4.77 in the testing set of 385 individuals) and no age-dependent bias. In an independent testing set of 100 individuals (19–65 years), we showed that the prediction accuracy could be further improved by using different CpG combinations and increasing the number of technical replicates (MAD of 4.17)

A strategy for multimodal data integration: application to biomarkers identification in spinocerebellar ataxia

International audienceThe growing number of modalities (e.g. multi-omics, imaging and clinical data) characterizing a given disease provides physicians and statisticians with complementary facets reflecting the disease process but emphasizes the need for novel statistical methods of data analysis able to unify these views. Such data sets are indeed intrinsically structured in blocks, where each block represents a set of variables observed on a group of individuals. Therefore, classical statistical tools cannot be applied without altering their organization, with the risk of information loss. Regularized generalized canonical correlation analysis (RGCCA) and its sparse generalized canonical correlation analysis (SGCCA) counterpart are component-based methods for exploratory analyses of data sets structured in blocks of variables. Rather than operating sequentially on parts of the measurements, the RGCCA/SGCCA-based integrative analysis method aims at summarizing the relevant information between and within the blocks. It processes a priori information defining which blocks are supposed to be linked to one another, thus reflecting hypotheses about the biology underlying the data blocks. It also requires the setting of extra parameters that need to be carefully adjusted. Here, we provide practical guidelines for the use of RGCCA/SGCCA. We also illustrate the flexibility and usefulness of RGCCA/SGCCA on a unique cohort of patients with four genetic subtypes of spinocerebellar ataxia, in which we obtained multiple data sets from brain volumetry and magnetic resonance spectroscopy, and metabolomic and lipidomic analyses. As a first step toward the extraction of multimodal biomarkers, and through the reduction to a few meaningful components and the visualization of relevant variables, we identified possible markers of disease progression

Effects of low dose radiation on atherosclerosis in APOE(-/-) mice: study of short term effects on macrophage polarization

International audienceAthersoclerosis is a chronic inflammatory disease of medium and large arteries that can lead to myocardial infarction or stroke. Mechanistic understanding of the effects of low-dose ionizing radiation (LDIR) on atherosclerosis remains incomplete. The experimental studies have shown a protective effect of LDIR on atherosclerosis in rodent models. However early responses of LDIR in different cell types that are known to be involved in atherosclerosis is not clear. The objective is to understand biological mechanisms of LDIR include on animal groups with multimodal approach. In this study, we report results of applying the foldchange, usually considered a relevant criterion for stating difference and similarity between measurements and a multilevel multivariate approach. Revealing complex correlations and causal links related to health conditions, such as atherosclerosis, can help advance the concept adverse outcome pathway (AOP)