Donepezil and memantine for moderate-to-severe Alzheimer's disease
- PMID: 22397651
- DOI: 10.1056/NEJMoa1106668
Donepezil and memantine for moderate-to-severe Alzheimer's disease
Abstract
Background: Clinical trials have shown the benefits of cholinesterase inhibitors for the treatment of mild-to-moderate Alzheimer's disease. It is not known whether treatment benefits continue after the progression to moderate-to-severe disease.
Methods: We assigned 295 community-dwelling patients who had been treated with donepezil for at least 3 months and who had moderate or severe Alzheimer's disease (a score of 5 to 13 on the Standardized Mini-Mental State Examination [SMMSE, on which scores range from 0 to 30, with higher scores indicating better cognitive function]) to continue donepezil, discontinue donepezil, discontinue donepezil and start memantine, or continue donepezil and start memantine. Patients received the study treatment for 52 weeks. The coprimary outcomes were scores on the SMMSE and on the Bristol Activities of Daily Living Scale (BADLS, on which scores range from 0 to 60, with higher scores indicating greater impairment). The minimum clinically important differences were 1.4 points on the SMMSE and 3.5 points on the BADLS.
Results: Patients assigned to continue donepezil, as compared with those assigned to discontinue donepezil, had a score on the SMMSE that was higher by an average of 1.9 points (95% confidence interval [CI], 1.3 to 2.5) and a score on the BADLS that was lower (indicating less impairment) by 3.0 points (95% CI, 1.8 to 4.3) (P<0.001 for both comparisons). Patients assigned to receive memantine, as compared with those assigned to receive memantine placebo, had a score on the SMMSE that was an average of 1.2 points higher (95% CI, 0.6 to 1.8; P<0.001) and a score on the BADLS that was 1.5 points lower (95% CI, 0.3 to 2.8; P=0.02). The efficacy of donepezil and of memantine did not differ significantly in the presence or absence of the other. There were no significant benefits of the combination of donepezil and memantine over donepezil alone.
Conclusions: In patients with moderate or severe Alzheimer's disease, continued treatment with donepezil was associated with cognitive benefits that exceeded the minimum clinically important difference and with significant functional benefits over the course of 12 months. (Funded by the U.K. Medical Research Council and the U.K. Alzheimer's Society; Current Controlled Trials number, ISRCTN49545035.).
Comment in
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Discontinuing donepezil or starting memantine for Alzheimer's disease.N Engl J Med. 2012 Mar 8;366(10):957-9. doi: 10.1056/NEJMe1200429. N Engl J Med. 2012. PMID: 22397659 No abstract available.
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Discontinuing donepezil or starting memantine for Alzheimer's disease.N Engl J Med. 2012 Jun 7;366(23):2227-8; author reply 2228. doi: 10.1056/NEJMc1204656. N Engl J Med. 2012. PMID: 22670911 No abstract available.
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Discontinuing donepezil or starting memantine for Alzheimer's disease.N Engl J Med. 2012 Jun 7;366(23):2227-8; author reply 2228. doi: 10.1056/NEJMc1204656. N Engl J Med. 2012. PMID: 22670912 No abstract available.
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ACP Journal Club. Donepezil or memantine improved cognitive functioning in moderate-to-severe Alzheimer disease.Ann Intern Med. 2012 Jun 19;156(12):JC6-10. doi: 10.7326/0003-4819-156-12-201206190-02010. Ann Intern Med. 2012. PMID: 22711111 No abstract available.
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Cessation of donepezil is associated with clinical decline in patients with moderate-to-severe Alzheimer's disease compared to continuation of donepezil or addition or substitution of memantine.Evid Based Med. 2013 Apr;18(2):62-3. doi: 10.1136/eb-2012-100722. Epub 2012 Jun 26. Evid Based Med. 2013. PMID: 22736656 No abstract available.
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