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Memantine in Alzheimer's disease: experience in an Alzheimer's disease assessment unit
Elena Sinforiani1, Chiara Pasotti, Laura Chiapella
1Alzheimer's Disease Assessment Unit/Laboratory of Neuropsychology, IRCCS C. Mondino National Institute of Neurology Foundation, Via Mondino 2, 27100 Pavia, Italy. elena.sinforiani@mondino.it
Background And Aims:
Memantine is an uncompetitive N-methyl-D-aspartate receptor antagonist. Clinical and observational studies have demonstrated its efficacy on both cognitive and behavioral symptoms of moderate-to-severe Alzheimer's disease (AD) and described its good safety and tolerability profile. We report here our experience with memantine in patients with AD during a two-year follow-up.
Methods:
From June 2005 to May 2010, memantine was given to 201 outpatients with moderate-to-severe AD: 93 patients were concomitantly receiving treatment with acetyl cholinesterase inhibitors (AChEIs) (Group 1) and the other 108 were prescribed memantine as monotherapy (Group 2). All patients were administered the following scales: Mini Mental State Examination, Activities of Daily Living, Instrumental Activities of Daily Living, Neuropsychiatric Inventory. We report the results of followup assessments conducted at six months and 1, 2 and 3 years.
Results:
Sixteen patients (8%) stopped treatment within the first month because of side-effects. In each group, about 20% of subjects showed no deterioration at six months and 1 year, and this proportion decreased only slightly at 2 years. Higher NPI scores at baseline and psychotropic drug use emerged as factors significantly related to reduced response to treatment (p<0.01).
Conclusions:
Results confirmed the short-term effect of memantine, both in monotherapy and in combination with AchEIs in moderate-to-severe AD. This efficacy, albeit slight, was found to persist in the longer term.
Insights
Memantine demonstrated sustained efficacy for moderate-to-severe Alzheimer's disease (AD) over two years, showing persistent benefits in cognitive and behavioral symptoms for many patients. The treatment was generally well-tolerated, with long-term effects observed in both monotherapy and combination treatments.
Area of Science:
- Neuroscience
- Pharmacology
Background:
- Memantine is an N-methyl-D-aspartate receptor antagonist with demonstrated efficacy in Alzheimer's disease (AD).
- Previous studies show memantine benefits cognitive and behavioral symptoms in moderate-to-severe AD with a good safety profile.
Purpose of the Study:
- To evaluate the long-term (two-year) experience with memantine in patients with moderate-to-severe Alzheimer's disease.
- To assess memantine's efficacy and tolerability in both monotherapy and combination with acetylcholinesterase inhibitors (AChEIs).
Main Methods:
- A two-year follow-up study of 201 outpatients with moderate-to-severe AD treated with memantine.
- Patients received either memantine monotherapy (n=108) or memantine with AChEIs (n=93).
- Standardized scales (MMSE, ADL, IADL, NPI) were used for assessments at multiple time points.
Main Results:
- 8% of patients discontinued memantine within the first month due to side-effects.
- Approximately 20% of patients in both groups showed no deterioration at six months and one year, with slight decreases at two years.
- Higher baseline NPI scores and psychotropic drug use were associated with reduced treatment response.
Conclusions:
- Memantine confirms short-term efficacy in moderate-to-severe AD, whether as monotherapy or combined with AChEIs.
- The observed efficacy of memantine persists into the longer term, albeit with slight reductions over time.
- Memantine is a viable treatment option for managing cognitive and behavioral symptoms in AD patients.
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