Deciphering the metabolome in Alzheimer's disease.
6 affiliations
- 1Program of Bone-Brain Axis Research, Department of Orthopedics, Institute on Aging and Brain Disorders, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
- 2Neurodegenerative Disorder Research Center, Hefei National Laboratory for Physical Sciences at the Microscale, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
- 3Program of Bone-Brain Axis Research, Department of Orthopedics, Institute on Aging and Brain Disorders, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China. [email protected].
- 4Neurodegenerative Disorder Research Center, Hefei National Laboratory for Physical Sciences at the Microscale, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China. [email protected].
- 5Center for Excellence in Brain Science and Intelligence Technology, Chinese Academy of Sciences, Shanghai, China. [email protected].
- 6Anhui Province Key Laboratory of Biomedical Aging Research, University of Science and Technology of China, Hefei, China. [email protected].
Abstract
Alzheimer's disease (AD), a multifaceted neurodegenerative disease, stands as the most prevalent form of dementia and one of the leading causes of death in the elderly. An increasing body of evidence underscores the intricate link between AD and metabolic disturbances. Metabolomics research has unveiled dysregulations in various metabolites within the brain and body fluids of individuals with AD, shedding light on the disease's metabolic underpinnings. Furthermore, notable correlations were identified between particular metabolites and AD-associated pathologies, as well as cognitive phenotypes, throughout the course of AD progression. Despite these valuable insights, a holistic understanding of the metabolic basis of AD is still scarce. This review examines recent studies investigating metabolome changes in different types of specimens from AD individuals. We presented a summary of the metabolic signatures of AD and the correlation between metabolites and AD-related traits. We then delineated the various biochemical pathways by which metabolites are involved in AD pathogenesis. We hope that this review will provide a basis for the further development of biomarkers and therapeutic strategies for metabolic disorders in AD.
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BibTeX
@article{yang2026deciphering,
title = {{Deciphering the metabolome in Alzheimer's disease.}},
author = {Xiaoli Yang and Yong Shen},
journal = {Molecular neurodegeneration},
year = {2026},
month = jul,
doi = {10.1186/s13024-026-00982-w},
url = {https://europepmc.org/article/MED/42972409},
note = {CC BY},
}
RIS
TY - JOUR
TI - Deciphering the metabolome in Alzheimer's disease.
AU - Xiaoli Yang
AU - Yong Shen
PY - 2026
DA - 2026/07/31
JO - Molecular neurodegeneration
DO - 10.1186/s13024-026-00982-w
UR - https://europepmc.org/article/MED/42972409
AB - Alzheimer's disease (AD), a multifaceted neurodegenerative disease, stands as the most prevalent form of dementia and one of the leading causes of death in the elderly. An increasing body of evidence underscores the intricate link between AD and metabolic disturbances. Metabolomics research has unveiled dysregulations in various metabolites within the brain and body fluids of individuals with AD, shedding light on the disease's metabolic underpinnings. Furthermore, notable correlations were identified between particular metabolites and AD-associated pathologies, as well as cognitive phenotypes, throughout the course of AD progression. Despite these valuable insights, a holistic understanding of the metabolic basis of AD is still scarce. This review examines recent studies investigating metabolome changes in different types of specimens from AD individuals. We presented a summary of the metabolic signatures of AD and the correlation between metabolites and AD-related traits. We then delineated the various biochemical pathways by which metabolites are involved in AD pathogenesis. We hope that this review will provide a basis for the further development of biomarkers and therapeutic strategies for metabolic disorders in AD.
SN - 1750-1326
ER -