队列
疾病
医学
海马结构
阿尔茨海默病
生物标志物
肿瘤科
淀粉样蛋白(真菌学)
神经科学
病理
心理学
内科学
生物
生物化学
作者
Min Kim,Stuart G. Snowden,Tommi Suvitaival,Ashfaq Ali,David J. Merkler,Tahmina Ahmad,Sarah Westwood,Alison L. Baird,Petroula Proitsi,Alejo Nevado‐Holgado,Abdul Hye,Isabelle Bos,Stephanie J. B. Vos,Rik Vandenberghe,Charlotte E. Teunissen,Mara ten Kate,Philip Scheltens,Silvy Gabel,Karen Meersmans,Olivier Blin
标识
DOI:10.1016/j.jalz.2019.03.004
摘要
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.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.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.PFAMs have been found increased and associated with amyloid β burden in CSF and clinical measures.
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