Long-term course and effectiveness of combination therapy in Alzheimer disease

被引:176
作者
Atri, Alireza [1 ,2 ,3 ]
Shaughnessy, Lynn W. [2 ,3 ,4 ]
Locascio, Joseph J. [2 ,3 ]
Growdon, John H. [2 ,3 ]
机构
[1] Massachusetts Gen Hosp, Memory Disorders Unit, Dept Neurol, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Massachusetts Alzheimers Dis Res Ctr, Boston, MA 02114 USA
[3] Harvard Univ, Sch Med, Boston, MA USA
[4] Massachusetts Sch Profess Psychol, W Roxbury, MA USA
关键词
treatment efficacy; modeling progression; cholinesterase inhibitor; memantine; memory; cognition and function in dementia;
D O I
10.1097/WAD.0b013e31816653bc
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To compare the real-world clinical effectiveness and long-term clinical trajectory in patients with Alzheimer disease (AD) treated with combination (COMBO) therapy consisting of cholinesterase-inhibitor (Cl) plus memantine (MEM) versus Cl alone versus no treatment with either. Methods: Three hundred eighty-two subjects with probable AD underwent serial clinical evaluations at a memory disorders unit. Cognition was assessed by the Information-Memory-Concentration subscale of the Blessed Dementia Scale (BDS) and function was assessed by the Weintraub Activities of Daily Living Scale (ADL) at 6-month intervals. One hundred forty-four subjects received standard care without CI or MEM (NORX), 122 received CI monotherapy, and 116 received COMBO therapy with Cl plus MEM. Mean follow-up was 30 months (4.1 visits) and mean cumulative medication treatment time was 22.5 months. Rates of decline were analyzed using mixed-effects regression models, and Cohen's d effect sizes were calculated annually for years 1 to 4. Results: Covarying for baseline scores, age, education, and duration of illness, the COMBO group had significantly lower mean annualized rates of deterioration in BDS and ADL scores compared with the CI (P < 0.001; Cohen's d(BDS) = 0.10 - 0.34 and (IADL = 0.23 - 0.46 at 1 to 2 y) and NO-RX groups (P < 0.001; Cohen's d(BDS) = 0.56 - 0.73 and d(ADL) = 0.32 - 0.48 at 1 to 2y). For the COMBO group, Cohen's d effect sizes increased with treatment duration. Similar comparisons significantly favored the CI over the NO-RX group on the BDS. Conclusions: COMBO therapy slows cognitive and functional decline in AD compared with Cl monotherapy and no treatment. These benefits had small-to-medium effect sizes that increased with time on treatment and were sustained for years.
引用
收藏
页码:209 / 221
页数:13
相关论文
共 53 条
[1]   An open-label, comparative study of rivastigmine, donepezil and galantamine in a real-world setting [J].
Aguglia, E ;
Onor, ML ;
Saina, M ;
Maso, E .
CURRENT MEDICAL RESEARCH AND OPINION, 2004, 20 (11) :1747-1752
[2]  
Aisen Paul S, 2006, Alzheimers Dement, V2, P272, DOI 10.1016/j.jalz.2006.08.004
[3]  
[Anonymous], 2002, ANAL LONGITUDINAL DA
[4]   Results of a multi-level therapeutic approach for Alzheimer's disease subjects in the "real world" (CRONOS project): a 36-week follow-up study [J].
Bellelli, G ;
Lucchi, E ;
Minicuci, N ;
Rozzini, L ;
Bianchetti, A ;
Padovani, A ;
Trabucchi, M .
AGING CLINICAL AND EXPERIMENTAL RESEARCH, 2005, 17 (01) :54-61
[5]  
Bentham P, 2004, LANCET, V363, P2105
[6]   Cholinesterase inhibitors for Alzheimer's disease [J].
Birks, J .
COCHRANE DATABASE OF SYSTEMATIC REVIEWS, 2006, (01)
[7]   ASSOCIATION BETWEEN QUANTITATIVE MEASURES OF DEMENTIA AND OF SENILE CHANGE IN CEREBRAL GREY MATTER OF ELDERLY SUBJECTS [J].
BLESSED, G ;
TOMLINSON, BE ;
ROTH, M .
BRITISH JOURNAL OF PSYCHIATRY, 1968, 114 (512) :797-+
[8]   A naturalistic study of galantamine for Alzheimer's disease [J].
Brodaty, Henry ;
Woodward, Michael ;
Boundy, Karyn ;
Barnes, Nicola ;
Allen, Gabrielle .
CNS DRUGS, 2006, 20 (11) :935-943
[9]   Naturalistic treatment of Alzheimer's disease with galantamine - 12-month follow-up from the NATURE study [J].
Brodaty, Henry ;
Woodward, Michael ;
Boundy, Karyn ;
Barnes, Nicola .
CNS DRUGS, 2007, 21 (04) :335-336
[10]   Efficacy and safety of donepezil over 3 years: an open-label, multicentre study in patients with Alzheimer's disease [J].
Burns, A. ;
Gauthier, S. ;
Perdomo, C. .
INTERNATIONAL JOURNAL OF GERIATRIC PSYCHIATRY, 2007, 22 (08) :806-812