JMIR Aging. 2025 Oct 8;8:e76981. doi: 10.2196/76981.
ABSTRACT
BACKGROUND: Neuroimaging is crucial in the diagnosis of Alzheimer disease (AD). In recent years, artificial intelligence (AI)-based neuroimaging technology has rapidly developed, providing new methods for accurate diagnosis of AD, but its performance differences still need to be systematically evaluated.
OBJECTIVE: This study aims to conduct a systematic review and meta-analysis comparing the diagnostic performance of AI-assisted fluorine-18 fluorodeoxyglucose positron emission tomography (18F-FDG PET) and structural magnetic resonance imaging (sMRI) for AD.
METHODS: Databases including Web of Science, PubMed, and Embase were searched from inception to January 2025 to identify original studies that developed or validated AI models for AD diagnosis using 18F-FDG PET or sMRI. Methodological quality was assessed using the TRIPOD-AI (Transparent Reporting of a Multivariable Prediction Model for Individual Prognosis or Diagnosis-Artificial Intelligence) checklist. A bivariate mixed-effects model was employed to calculate pooled sensitivity, specificity, and summary receiver operating characteristic curve area (SROC-AUC).
RESULTS: A total of 38 studies were included, with 28 moderate-to-high-quality studies analyzed. Pooled SROC-AUC values were 0.94 (95% CI 0.92-0.96) for sMRI and 0.96 (95% CI 0.94-0.98) for 18F-FDG PET, demonstrating statistically significant intermodal differences (P=.02). Subgroup analyses revealed that for machine learning, pooled SROC-AUCs were 0.89 (95% CI 0.86-0.92) for sMRI and 0.95 (95% CI 0.92-0.96) for 18F-FDG PET, while for deep learning, these values were 0.96 (95% CI 0.94-0.97) and 0.97 (95% CI 0.96-0.99), respectively. Meta-regression identified heterogeneity arising from study quality stratification, algorithm types, and validation strategies.
CONCLUSIONS: Both AI-assisted 18F-FDG PET and sMRI exhibit high diagnostic accuracy in AD, with 18F-FDG PET demonstrating superior overall diagnostic performance compared to sMRI.
PMID:41061249 | DOI:10.2196/76981
