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INTRODUCTION: A critical and as-yet unmet need in Alzheimer's disease (AD) is the discovery of peripheral small molecule biomarkers. Given that brain pathology precedes clinical symptom onset, we set out to test whether metabolites in blood associated with pathology as indexed by cerebrospinal fluid (CSF) AD biomarkers. METHODS: This study analyzed 593 plasma samples selected from the European Medical Information Framework for Alzheimer's Disease Multimodal Biomarker Discovery study, of individuals who were cognitively healthy (n = 242), had mild cognitive impairment (n = 236), or had AD-type dementia (n = 115). Logistic regressions were carried out between plasma metabolites (n = 883) and CSF markers, magnetic resonance imaging, cognition, and clinical diagnosis. RESULTS: Eight metabolites were associated with amyloid β and one with t-tau in CSF, these were primary fatty acid amides (PFAMs), lipokines, and amino acids. From these, PFAMs, glutamate, and aspartate also associated with hippocampal volume and memory. DISCUSSION: PFAMs have been found increased and associated with amyloid β burden in CSF and clinical measures.

More information Original publication

DOI

10.1016/j.jalz.2019.03.004

Type

Journal article

Publication Date

2019-06-01T00:00:00+00:00

Volume

15

Pages

817 - 827

Total pages

10

Keywords

Alzheimer's disease, Amyloid, Biomarkers, Brain volume measurements, CSF, Cognitive function measurements, Dementia, EMIF-AD, Metabolomics, Tau, Aged, Amyloid beta-Peptides, Amyloidosis, Biomarkers, Brain, Cognitive Dysfunction, Cohort Studies, Female, Hippocampus, Humans, Magnetic Resonance Imaging, Male, Memory, Metabolomics, Middle Aged, Neuropsychological Tests, tau Proteins