Longitudinal Analysis of Amyloid PET and Brain MRI for Predicting Conversion from Mild Cognitive Impairment to Alzheimer's Disease: Findings from the ADNI Cohort

淀粉样蛋白PET和脑部MRI纵向分析预测轻度认知障碍向阿尔茨海默病转化:来自ADNI队列的研究结果

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Abstract

BACKGROUND/OBJECTIVES: This study aimed to investigate the predictive power of integrated longitudinal amyloid positron emission tomography (PET) and brain magnetic resonance imaging (MRI) data for determining the likelihood of conversion to Alzheimer's disease (AD) in patients with mild cognitive impairment (MCI). METHODS: We included 180 patients with MCI from the Alzheimer's Disease Neuroimaging Initiative, with baseline and 2-year follow-up scans obtained using F-18 florbetapir PET and MRI. Patients were categorized as converters (progressing to AD) or nonconverters based on a 6-year follow-up. Quantitative analyses included the calculation of amyloid burden using the standardized uptake value ratio (SUVR), brain amyloid smoothing scores (BASSs), brain atrophy indices (BAIs), and their integration into shape features. Longitudinal changes and receiver operating characteristic analyses assessed the predictive power of these biomarkers. RESULTS: Among 180 patients with MCI, 76 (42.2%) were converters, who exhibited significantly higher baseline and 2-year follow-up values for SUVR, BASS, BAI, and shape features than nonconverters (p < 0.001). Shape features demonstrated the highest predictive accuracy for conversion, with areas under the curve of 0.891 at baseline and 0.898 at 2 years. Percent change analyses revealed significant increases in brain atrophy; amyloid deposition changes showed a paradoxical decrease in converters. Additionally, strong associations were observed between longitudinal changes in shape features and neuropsychological test results. CONCLUSIONS: The integration of amyloid PET and MRI biomarkers enhances the prediction of AD progression in patients with MCI. These findings support the potential of combined imaging approaches for early diagnosis and targeted interventions in AD.

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