AI Article Synopsis

  • Alzheimer's disease (AD) is a serious neurodegenerative condition, making early identification of its progression from normal cognition to mild cognitive impairment (MCI) crucial.
  • The study utilized a multimodal support vector machine, analyzing MRI and PET data from two groups, revealing a classification accuracy of 67.5% for identifying individuals at risk of MCI or AD.
  • Results showed improved accuracy (70%) and sensitivity (75%) when feature selection was applied, indicating that combining different data sources is more effective than using a single method in diagnosing AD progression.

Article Abstract

Alzheimer's disease (AD) is one of the most serious progressive neurodegenerative diseases among the elderly, therefore the identification of conversion to AD at the earlier stage has become a crucial issue. In this study, we applied multimodal support vector machine to identify the conversion from normal elderly cognition to mild cognitive impairment (MCI) or AD based on magnetic resonance imaging and positron emission tomography data. The participants included two independent cohorts (Training set: 121 AD patients and 120 normal controls (NC); Testing set: 20 NC converters and 20 NC non-converters) from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database. The multimodal results showed that the accuracy, sensitivity, and specificity of the classification between NC converters and NC non-converters were 67.5% , 73.33% , and 64% , respectively. Furthermore, the classification results with feature selection increased to 70% accuracy, 75% sensitivity, and 66.67% specificity. The classification results using multimodal data are markedly superior to that using a single modality when we identified the conversion from NC to MCI or AD. The model built in this study of identifying the risk of normal elderly converting to MCI or AD will be helpful in clinical diagnosis and pathological research.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6287610PMC
http://dx.doi.org/10.3233/JAD-142820DOI Listing

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