Alzheimer’s disease (AD) could be described into following four stages: healthy control (HC), early mild cognitive impairment (EMCI), late MCI (LMCI) and AD dementia. The discriminations between different stages of AD are considerably important issues for future pre-dementia treatment. However, it is still challenging to identify LMCI from EMCI because of the subtle changes in imaging which are not noticeable. In addition, there were relatively few studies to make inferences about the brain dynamic changes in the cognitive progression from EMCI to LMCI to AD. Inspired by the above problems, we proposed an advanced approach of evolutionary weighted random support vector machine cluster (EWRSVMC). Where the predictions of numerous weighted SVM classifiers are aggregated for improving the generalization performance. We validated our method in multiple binary classifications using Alzheimer’s Disease Neuroimaging Initiative dataset. As a result, the encouraging accuracy of 90% for EMCI/LMCI and 88.89% for LMCI/AD were achieved respectively, demonstrating the excellent discriminating ability. Furthermore, disease-related brain regions underlying the AD progression could be found out on the basis of the amount of discriminative information. The findings of this study provide considerable insight into the neurophysiological mechanisms in AD development.

The identification of abnormal cognitive decline at an early stage becomes an increasingly significant conundrum to physicians and is of major interest in the studies of mild cognitive impairment (MCI). Support vector machine (SVM) as a high-dimensional pattern classification technique is widely employed in neuroimaging research. However, the application of a single SVM classifier may be difficult to achieve the excellent classification performance because of the small-sample size and noise of imaging data. To address this issue, we propose a novel method of the weighted random support vector machine cluster (WRSVMC) in which multiple SVMs were built and different weights were given to corresponding SVMs with different classification performances. We evaluated our algorithm on resting state functional magnetic resonance imaging (RS-fMRI) data of 93 MCI patients and 105 healthy controls (HC) from the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort. The maximum accuracy given by the WRSVMC is 87.67%, demonstrating excellent diagnostic power. Furthermore, the most discriminative brain areas have been found out as follows: gyrus rectus (REC.L), precentral gyrus (PreCG.R), olfactory cortex (OLF.L), and middle occipital gyrus (MOG.R). These findings of the paper provide a new perspective for the clinical diagnosis of MCI.

Asperger syndrome (AS) is subtype of autism spectrum disorder (ASD). Diagnosis and pathological analysis of AS through resting-state fMRI data is one of the hot topics in brain science. We employed a new model called the genetic-evolutionary random Support Vector Machine cluster (GE-RSVMC) to classify AS and normal people, and search for lesions. The model innovatively integrates the methods of the cluster and genetic evolution to improve the performance of the model. We randomly selected samples and sample features to construct GE-RSVMC, and then used the cluster to classify and extract lesions according to classification results. The model was validated by data of 157 participants (86 AS and 71 health controls) in ABIDE database. The classification accuracy of the model reached to 97.5% and we discovered the brain regions with significant differences, such as the Angular gyrus (ANG.R), Precuneus (PCUN.R), Caudate nucleus (CAU.R), Cuneus (CUN.R) and so on. Our method provides a new perspective for the diagnosis and treatment of AS, and a universal framework for other brain science research as the model has excellent generalization performance.

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