Abstract

Assessing dementia conversion in patients with mild cognitive impairment (MCI) remains challenging owing to pathological heterogeneity. While many MCI patients ultimately proceed to Alzheimer’s disease (AD), a subset of patients remain stable for various times. Our aim was to characterize the plasma metabolites of nineteen MCI patients proceeding to AD (P-MCI) and twenty-nine stable MCI (S-MCI) patients by untargeted metabolomics profiling. Alterations in the plasma metabolites between the P-MCI and S-MCI groups, as well as between the P-MCI and AD groups, were compared over the observation period. With the help of machine learning-based stratification, a 20-metabolite signature panel was identified that was associated with the presence and progression of AD. Furthermore, when the metabolic signature panel was used for classification of the three patient groups, this gave an accuracy of 73.5% using the panel. Moreover, when specifically classifying the P-MCI and S-MCI subjects, a fivefold cross-validation accuracy of 80.3% was obtained using the random forest model. Importantly, indole-3-propionic acid, a bacteria-generated metabolite from tryptophan, was identified as a predictor of AD progression, suggesting a role for gut microbiota in AD pathophysiology. Our study establishes a metabolite panel to assist in the stratification of MCI patients and to predict conversion to AD.

Highlights

  • IntroductionClinical trials testing Alzheimer’s disease (AD) disease-modifying therapies have failed to provide any promising solutions [2]

  • To investigate the association of the plasma metabolites with Alzheimer’s disease (AD) conversion, we focused on the longitudinal data collected from the mild cognitive impairment (MCI) patients who proceeded to AD (P-MCI subjects, n = 19); these are the patients that underwent MCI-to-AD conversion during the observation period

  • The MCI patients who remained MCI or exhibited an alleviation of symptoms over the 3- to 5-year study period were defined as stable MCI (S-MCI, n = 29)

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Summary

Introduction

Clinical trials testing AD disease-modifying therapies have failed to provide any promising solutions [2]. In this context, two new directions for AD therapeutic development have been proposed. That possible pathological mechanisms other than the amyloid-driven hypothesis should be explored and, secondly, that individuals during the early stages of AD should be identified, with this being the time frame in which intervention is most likely to be possible. With respect to AD diagnosis, mild cognitive impairment (MCI) is often considered to be the prodromal stage of clinically diagnosed

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