4.7 Article

Risk Prediction of Alzheimer's Disease Conversion in Mild Cognitive Impaired Population Based on Brain Age Estimation

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IEEE-INST ELECTRICAL ELECTRONICS ENGINEERS INC
DOI: 10.1109/TNSRE.2023.3247590

关键词

Estimation; Brain modeling; Magnetic resonance imaging; Hazards; Analytical models; Alzheimer's disease; Neuroimaging; conversion risk prediction; brain age; cox hazard analysis; nomogram

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Alzheimer's disease (AD) is a common neurodegenerative disease and it's important to assess the AD conversion risk of MCI individuals. This study proposes an AD conversion risk estimation system (CRES) that utilizes MRI data to estimate brain age and evaluate AD conversion risk. Results show that the MRI derived age gap significantly distinguishes different groups and each additional year in age gap is associated with a 4.57% greater risk of AD conversion for MCI subjects. Furthermore, a nomogram is drawn to predict the individual MCI conversion risk. The CRES provides valuable information for early intervention and diagnosis.
Alzheimer's disease (AD) is one of the most common neurodegenerative diseases in the world. To reduce the incidence of AD, it's essential to quantify the AD conversion risk of mild cognitive impaired (MCI) individuals. Here, we propose an AD conversion risk estimation system (CRES), which contains an automated MRI feature extractor, brain age estimation (BAE) module, and AD conversion risk estimation module. The CRES is trained on 634 normal controls (NC) from the public IXI and OASIS cohorts, then it is evaluated on 462 subjects (106 NC, 102 stable MCI (sMCI), 124 progressive MCI (pMCI) and 130 AD) from the ADNI dataset. Experimental results show that the MRI derived age gap (AG, chronological age subtracted from the estimated brain age) significantly distinguish NC, sMCI, pMCI and AD groups with p-value = 0.000017. Considering AG as the primary factor, incorporating gender and Minimum Mental State Examination (MMSE) for more robust Cox multi-variate hazard analysis, we concluded that each additional year in AG is associated with 4.57% greater AD conversion risk for the MCI group. Furthermore, a nomogram was drawn to describe MCI conversion risk at the individual level in the next 1 year, 3 years, 5 years and even 8 years from baseline. This work demonstrates that CRES can estimate AG based on MRI data, evaluate AD conversion risk of the MCI subjects, and identify the individuals with high AD conversion risk, which is valuable for effective intervention and diagnosis within an early period.

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