Metabolic neuroimaging of ApoE and APP mutational status in mouse models of Alzheimer’s disease

Motivation: As metabolic impairment is key in AD, metabolic imaging could potentially improve diagnosis and monitoring of AD. Goal(s): Our goal is to determine which metabolic imaging approach, or combination of approaches, provide the optimal set of biomarkers for AD. Approach: We combined three metabolic imaging methods, 1H MRS, HP 13C MRSI and 18F-FDG PET, with machine learning to characterize the neurometabolic profiles linked to AD-related risk factors, namely ApoE mutation, APP mutation, and sex in AD mouse models. Results: Combining metabolic neuroimaging and machine learning can help discriminate between AD-related mutational status (APP and ApoE) and provide information of AD-related sexual dimorphism. Impact: Knowing which metabolic imaging approach(es) is/are optimal to monitor progression in each subset of AD patients, based on sex and mutational status, would improve patient-centric clinical care and potentially create new avenues for assessment of new metabolism-targeting therapies.

Authors

Publication Details

Journal
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Published
2024-11-26
DOI
https://doi.org/10.58530/2024/0966
Primary Topic
Bioinformatics and Genomic Networks
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Metabolic neuroimaging of ApoE and APP mutational status in mouse models of Alzheimer’s disease

Lydia M. Le Page, Caroline Guglielmetti, Marina Radoul, Yadong Huang et al.
Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Bioinformatics and Genomic Networks
article

Metabolic neuroimaging of ApoE and APP mutational status in mouse models of Alzheimer’s disease

Lydia M. Le Page, Caroline Guglielmetti, Marina Radoul, Yadong Huang, Ken Nakamura, Yoshitaka Sei, Myriam M. Chaumeil, Huihui Li, Xiao Gao
article en

Abstract

Motivation: As metabolic impairment is key in AD, metabolic imaging could potentially improve diagnosis and monitoring of AD. Goal(s): Our goal is to determine which metabolic imaging approach, or combination of approaches, provide the optimal set of biomarkers for AD. Approach: We combined three metabolic imaging methods, 1H MRS, HP 13C MRSI and 18F-FDG PET, with machine learning to characterize the neurometabolic profiles linked to AD-related risk factors, namely ApoE mutation, APP mutation, and sex in AD mouse models. Results: Combining metabolic neuroimaging and machine learning can help discriminate between AD-related mutational status (APP and ApoE) and provide information of AD-related sexual dimorphism. Impact: Knowing which metabolic imaging approach(es) is/are optimal to monitor progression in each subset of AD patients, based on sex and mutational status, would improve patient-centric clinical care and potentially create new avenues for assessment of new metabolism-targeting therapies.

Proceedings on CD-ROM - International Society for Magnetic Resonance in Medicine. Scientific Meeting and Exhibition/Proceedings of the International Society for Magnetic Resonance in Medicine, Scientific Meeting and Exhibition
Reduced inequalities
Openalex Percentile: Top 81%
Bioinformatics and Genomic Networks
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.