Related Experiment Video
Updated: Dec 27, 2025

Application of Granger Causality Analysis of the Directed Functional Connection in Alzheimer's Disease and Mild Cognitive Impairment
Published on: August 7, 2017
MRI Radiomics Classification and Prediction in Alzheimer's Disease and Mild Cognitive Impairment: A Review
Qi Feng1, Zhongxiang Ding1,2
1Department of Radiology, Affiliated Hangzhou First People's Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Background:
Alzheimer's Disease (AD) is a progressive neurodegenerative disease that threatens the health of the elderly. Mild Cognitive Impairment (MCI) is considered to be the prodromal stage of AD. To date, AD or MCI diagnosis is established after irreversible brain structure alterations. Therefore, the development of new biomarkers is crucial to the early detection and treatment of this disease. At present, there exist some research studies showing that radiomics analysis can be a good diagnosis and classification method in AD and MCI.
Objective:
An extensive review of the literature was carried out to explore the application of radiomics analysis in the diagnosis and classification among AD patients, MCI patients, and Normal Controls (NCs).
Results:
Thirty completed MRI radiomics studies were finally selected for inclusion. The process of radiomics analysis usually includes the acquisition of image data, Region of Interest (ROI) segmentation, feature extracting, feature selection, and classification or prediction. From those radiomics methods, texture analysis occupied a large part. In addition, the extracted features include histogram, shapebased features, texture-based features, wavelet features, Gray Level Co-Occurrence Matrix (GLCM), and Run-Length Matrix (RLM).
Conclusion:
Although radiomics analysis is already applied to AD and MCI diagnosis and classification, there still is a long way to go from these computer-aided diagnostic methods to the clinical application.
Insights
Radiomics analysis shows promise for diagnosing Alzheimer's Disease (AD) and Mild Cognitive Impairment (MCI) by analyzing MRI data. Further development is needed for clinical application of these early detection biomarkers.
Area of Science:
- Neuroimaging
- Biomarker Discovery
- Medical Informatics
Background:
- Alzheimer's Disease (AD) and Mild Cognitive Impairment (MCI) are neurodegenerative conditions often diagnosed after irreversible brain changes.
- Early detection biomarkers are crucial for timely intervention and treatment of AD and MCI.
- Current diagnostic methods for AD and MCI lack the sensitivity for early detection.
Purpose of the Study:
- To review the literature on radiomics analysis for diagnosing and classifying AD and MCI.
- To explore the potential of radiomics as an early detection biomarker for neurodegenerative diseases.
- To assess the current state and future directions of radiomics in AD and MCI research.
Main Methods:
- Extensive literature review of MRI radiomics studies.
- Inclusion of 30 completed radiomics studies.
- Analysis of radiomics methodologies including image acquisition, ROI segmentation, feature extraction, and classification.
Main Results:
- Radiomics analysis, particularly texture analysis, is being explored for AD and MCI diagnosis.
- Commonly extracted features include histogram, shape, texture, wavelet, GLCM, and RLM.
- Studies indicate radiomics can aid in the diagnosis and classification of AD and MCI.
Conclusions:
- Radiomics analysis demonstrates potential as a diagnostic and classification tool for AD and MCI.
- Significant advancements in computer-aided diagnostic methods are emerging.
- Further research and development are required to translate radiomics into routine clinical practice for early AD and MCI detection.
More Related Videos
Related Concept Videos
Alzheimer's Disease: Overview
The clinical diagnosis of AD hinges on the presence of memory and other cognitive impairments. Biomarkers, such as changes in Aβ...
Magnetic Resonance Imaging
Imaging Studies for Cardiovascular System IV: CMRI
Alzheimer's Disease: Treatment

