Abstract

BackgroundCholinesterase inhibitors (ChEIs) are an FDA-approved symptomatic treatment for patients with Alzheimer’s disease (AD). Its efficacy in patients with mild cognitive impairment (MCI), however, is controversial. Nonetheless, ChEIs have often been used in patients with MCI. From the perspective that ChEIs were developed based on the pathomechanism of AD, the effect of ChEIs in MCI patients could be different depending on the amyloid burden. In this retrospective observational study, we aimed to investigate the influence of ChEIs and amyloid burden on cognitive change for 1 year in patients with MCI.MethodsWe included 111 patients with MCI with a Clinical Dementia Rating (CDR) score of 0.5, a 1-year follow-up cognitive assessment, and amyloid positron emission tomography (PET) performed within 6 months before or after the baseline cognitive assessment (73 ChEI users and 38 ChEI non-users) from the Neurocognitive Behavior Center of Seoul National University Bundang Hospital. Additionally, those who had a positive amyloid PET scan more than 6 months before the baseline cognitive assessment and those who had a negative amyloid PET scan more than 6 months after the 1-year follow-up cognitive assessment were also included. Among the total 111 patients, 25 ChEI users and 25 ChEI non-users were matched by baseline Mini-Mental State Examination (MMSE) score, age, educational level, CDR Sum of Boxes, and amyloid PET positivity using propensity score matching. Multiple linear regression analysis was performed to assess the influence of ChEI use and amyloid PET positivity on cognitive change for 1 year. Univariate and multivariate logistic regression analyses were performed to evaluate the association between ChEI use and disease progression to CDR 1 at the 1-year follow-up visit.ResultsChEI use or non-use was not associated with cognitive change for 1 year. Amyloid PET positivity or negativity did not change this non-association. Furthermore, progression to CDR 1 was related to low baseline MMSE score (OR 0.606, CI 0.381–0.873), but not with ChEI use or non-use, and not with amyloid PET result.ConclusionChEI use or non-use was not related to cognitive change at a 1-year follow-up visit in patients with or without amyloid burden. In addition, ChEI use or non-use could not predict disease progression to CDR 1 at 1-year follow-up visit.

Highlights

  • Cholinesterase inhibitors (ChEIs) are an Food and Drug Administration (FDA)-approved symptomatic treatment for patients with Alzheimer’s disease (AD)

  • According to a study with the Alzheimer’s Disease Neuroimaging Initiative (ADNI) cohort, 44% of the recruited patients with mild cognitive impairment (MCI) were treated with ChEIs [2]

  • As ChEIs were developed based on pathological changes in early AD, evaluation of the effect of ChEIs in patients with MCI with AD pathology confirmed by AD biomarkers might provide useful clues to ChEI use regarding the timing of initiating therapy or the indications for treatment

Read more

Summary

Introduction

Cholinesterase inhibitors (ChEIs) are an FDA-approved symptomatic treatment for patients with Alzheimer’s disease (AD). From the perspective that ChEIs were developed based on the pathomechanism of AD, the effect of ChEIs in MCI patients could be different depending on the amyloid burden. Cholinesterase inhibitors (ChEIs) are a Food and Drug Administration (FDA)-approved symptomatic treatment for Alzheimer’s disease (AD) and include donepezil, rivastigmine, and galantamine. Their efficacy in mild cognitive impairment (MCI) is uncertain. As ChEIs were developed based on pathological changes in early AD, evaluation of the effect of ChEIs in patients with MCI with AD pathology confirmed by AD biomarkers might provide useful clues to ChEI use regarding the timing of initiating therapy or the indications for treatment

Objectives
Methods
Results
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call