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Abstract #0567

Neurometabolic Signatures of Cognitive Resilience in Alzheimer's Disease: A Hybrid 3D-MRSI/PET Study

Wenli Li1, Miao Zhang2, Yibo Zhao3, Yudu Li3,4,5, Wen Jin3,6, Yaoyu Zhang1, Jialin Hu1, Zhi-Pei Liang3,6, and Yao Li1,7
1National Engineering Research Center of Advanced Magnetic Resonance Technologies for Diagnosis and Therapy (NERC-AMRT), School of Biomedical Engineering, Shanghai Jiao Tong University, Shanghai, China, 2Department of Nuclear Medicine, Ruijin Hospital, Shanghai, China, 3Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Champaign, IL, United States, 4Department of Bioengineering, University of Illinois at Urbana-Champaign, Champaign, IL, United States, 5National Center for Supercomputing Applications, University of Illinois at Urbana-Champaign, Champaign, IL, United States, 6Department of Electrical and Computer Engineering, University of Illinois at Urbana-Champaign, Champaign, IL, United States, 7Institute of Medical Robotics, Shanghai Jiao Tong University, Shanghai, China

Synopsis

Keywords: Alzheimer's Disease, Alzheimer's Disease

Motivation: To explore neurometabolic features underlying cognitive resilience (CR) in Alzheimer’s disease (AD).

Goal(s): To identify the neurometabolic signatures of CR that mitigate AD-related glucose hypometabolism on cognition using combined 3D 1H-MRSI and PET imaging.

Approach: We conducted high-resolution, whole-brain 1H-MRSI and 18F-FDG PET imaging with cognitive assessments in 245 participants (114 AD, 50 MCI and 81 controls). Interactions between neurometabolic changes and glucose hypometabolism across cognitive domains were analyzed.

Results: Higher N-acetyl aspartate and lower myo-inositol levels in the temporal lobe mitigated the effects of hypometabolism on global cognitive function. Distinct neurometabolic changes support resilience across different cognitive domains.

Impact: Higher NAA/Cr and lower mI/Cr levels in the parietal and temporal lobes may serve as promising markers of CR in AD. These neurometabolic signatures may provide insights into intervention strategies aimed at slowing cognitive decline in AD.

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