Abstract

ObjectiveTo investigate whether cholinesterase inhibitors (ChEIs) are associated with slower cognitive decline in Alzheimer dementia and decreased risk of severe dementia or death.MethodsPatients with Alzheimer dementia from the Swedish Dementia Registry starting on ChEIs within 3 months of the dementia diagnosis were included and compared to nontreated patients with Alzheimer dementia. In a propensity score–matched cohort, the association between ChEI use and cognitive trajectories assessed by Mini-Mental State Examination (MMSE) scores was examined with a mixed model, and severe dementia (MMSE score <10) or death as an outcome was assessed with Cox proportional hazards models.ResultsThe matched cohort included 11,652 ChEI users and 5,826 nonusers. During an average of 5 years of follow-up, 255 cases developed severe dementia, and 6,055 (35%) died. ChEI use was associated with higher MMSE score at each visit (0.13 MMSE points per year; 95% confidence interval [CI] 0.06–0.20). ChEI users had a 27% lower risk of death (0.73, 95% CI 0.69–0.77) compared with nonusers. Galantamine was associated with lower risk of death (0.71, 95% CI 0.65–0.76) and lower risk of severe dementia (0.69, 95% CI 0.47–1.00) and had the strongest effect on cognitive decline of all the ChEIs (0.18 MMSE points per year, 95% CI 0.07–0.28).ConclusionsChEIs are associated with cognitive benefits that are modest but persist over time and with reduced mortality risk, which could be explained partly by their cognitive effects. Galantamine was the only ChEI demonstrating a significant reduction in the risk of developing severe dementia.Classification of EvidenceThis study provides Class III evidence that for patients with Alzheimer dementia ChEIs decrease long-term cognitive decline and risk of death and that galantamine decreases the risk of severe dementia.

Highlights

  • The acetylcholinesterase inhibitors (ChEIs) and the NMDA-receptor antagonist memantine are hitherto the only specific pharmacological treatments approved for Alzheimers dementia, the most common cause of dementia[1]

  • ChEIs are associated with cognitive benefits which are modest but persist over time and with reduced mortality risk, which could be explained partly by their cognitive effects

  • Galantamine was the only ChEI demonstrating a significant reduction in the risk of developing severe dementia

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Summary

Introduction

The acetylcholinesterase inhibitors (ChEIs) and the NMDA-receptor antagonist memantine are hitherto the only specific pharmacological treatments approved for Alzheimers dementia, the most common cause of dementia[1]. Their benefit appears to be modest[2, 3], a significant body of evidence supports their effectiveness for improving cognition as well as their costeffectivenesss[4,5,6,7,8,9,10,11,12]. Not RCTs, follow-up of ChEI-treated Alzheimers dementia cohorts has shown small cognitive benefits at 2-, 3- and more than 10-years[23,24,25]. Other studies have shown associations between ChEI-use and decreased risk of myocardial infarction, stroke and death in patients with dementia[27,28,29,30]

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