Differential Efficacy of Treatment with Acetylcholinesterase Inhibitors in Patients with Mild and Moderate Alzheimer’s Disease over a 6-Month Period
There are various anticholinesterase inhibitors (AChEIs) for the symptomatic treatment of mild to moderate Alzheimer’s disease (AD). All AChEIs have shown greater efficacy than placebo in randomized, double-blind, parallel-group clinical trials. No differential studies have yet been made of the effi...
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creator | López-Pousa, S. Turon-Estrada, A. Garre-Olmo, J. Pericot-Nierga, I. Lozano-Gallego, M. Vilalta-Franch, M. Hernández-Ferràndiz, M. Morante-Muñoz, V. Isern-Vila, A. Gelada-Batlle, E. Majó-Llopart, J. |
description | There are various anticholinesterase inhibitors (AChEIs) for the symptomatic treatment of mild to moderate Alzheimer’s disease (AD). All AChEIs have shown greater efficacy than placebo in randomized, double-blind, parallel-group clinical trials. No differential studies have yet been made of the efficacy between all AChEIs. The study aims to determine the differential efficacy of the AChEIs with respect to a historical sample of patients with AD that were not treated with AChEIs. An open-label, prospective, observational study with a retrospective control group was undertaken to examine the evolution of the cognitive function over a 6-month period. The patients were assessed with the Mini-Mental State Examination (MMSE) at study entry and at 6 months. A general linear model was applied for repeated measurements with the MMSE score as the dependent variable, treatment type as an independent variable and the severity of the deterioration, age and the MMSE baseline score as covariables. Of the sample of 147 patients, 40 initiated treatment with donepezil, 32 with galantamine, 30 with rivastigmine and 45 were part of a historical sample of the memory clinic patients between 1991 and 1996 that had not been treated with AChEIs. The average age was 73.7 years (SD = 6.9; range = 52–86), 67.3% were women, 78.2% of the cases were mild and the MMSE baseline score was 18.1 points (range = 11–27). No significant intergroup differences were observed in these variables. The average doses of donepezil, galantamine and rivastigmine were 5.87 mg/day (SD = 1.92), 14.81 mg/day (SD = 6.25) and 6.41 mg/day (SD = 1.82), respectively. At 6 months, the difference in the MMSE score with respect to the untreated group was 1.6 points for donepezil (95% CI 0.79–2.37; p < 0.001), 0.99 points for galantamine (95% CI 0.14–1.85; p = 0.01) and 0.90 points for rivastigmine (95% CI 0.05–1.74; p = 0.03). No significant differences were observed in the efficacy among the groups treated with AChEIs (p > 0.05). Treatment with AChEIs significantly delays the global cognitive impairment associated with AD for at least 6 months. Our study found no significant differences in efficacy between donepezil, galantamine and rivastigmine. Further studies in the context of daily clinical practice will determine the clinical significance of the changes observed. An important variability of the response to the treatment was observed in treated patients. |
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All AChEIs have shown greater efficacy than placebo in randomized, double-blind, parallel-group clinical trials. No differential studies have yet been made of the efficacy between all AChEIs. The study aims to determine the differential efficacy of the AChEIs with respect to a historical sample of patients with AD that were not treated with AChEIs. An open-label, prospective, observational study with a retrospective control group was undertaken to examine the evolution of the cognitive function over a 6-month period. The patients were assessed with the Mini-Mental State Examination (MMSE) at study entry and at 6 months. A general linear model was applied for repeated measurements with the MMSE score as the dependent variable, treatment type as an independent variable and the severity of the deterioration, age and the MMSE baseline score as covariables. Of the sample of 147 patients, 40 initiated treatment with donepezil, 32 with galantamine, 30 with rivastigmine and 45 were part of a historical sample of the memory clinic patients between 1991 and 1996 that had not been treated with AChEIs. The average age was 73.7 years (SD = 6.9; range = 52–86), 67.3% were women, 78.2% of the cases were mild and the MMSE baseline score was 18.1 points (range = 11–27). No significant intergroup differences were observed in these variables. The average doses of donepezil, galantamine and rivastigmine were 5.87 mg/day (SD = 1.92), 14.81 mg/day (SD = 6.25) and 6.41 mg/day (SD = 1.82), respectively. At 6 months, the difference in the MMSE score with respect to the untreated group was 1.6 points for donepezil (95% CI 0.79–2.37; p < 0.001), 0.99 points for galantamine (95% CI 0.14–1.85; p = 0.01) and 0.90 points for rivastigmine (95% CI 0.05–1.74; p = 0.03). No significant differences were observed in the efficacy among the groups treated with AChEIs (p > 0.05). Treatment with AChEIs significantly delays the global cognitive impairment associated with AD for at least 6 months. Our study found no significant differences in efficacy between donepezil, galantamine and rivastigmine. Further studies in the context of daily clinical practice will determine the clinical significance of the changes observed. An important variability of the response to the treatment was observed in treated patients.</description><identifier>ISSN: 1420-8008</identifier><identifier>EISSN: 1421-9824</identifier><identifier>DOI: 10.1159/000083498</identifier><identifier>PMID: 15677866</identifier><identifier>CODEN: DGCDFX</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Aged ; Aged, 80 and over ; Alzheimer Disease - diagnosis ; Alzheimer Disease - drug therapy ; Biological and medical sciences ; Cardiovascular system ; Cholinesterase Inhibitors - administration & dosage ; Cholinesterase Inhibitors - therapeutic use ; Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases ; Drug Administration Schedule ; Female ; Galantamine - administration & dosage ; Galantamine - therapeutic use ; Humans ; Indans - administration & dosage ; Indans - therapeutic use ; Male ; Medical sciences ; Middle Aged ; Neurology ; Neuropsychological Tests ; Original Research Article ; Pharmacology. Drug treatments ; Phenylcarbamates - administration & dosage ; Phenylcarbamates - therapeutic use ; Piperidines - administration & dosage ; Piperidines - therapeutic use ; Prospective Studies ; Retrospective Studies ; Rivastigmine ; Severity of Illness Index ; Time Factors ; Vascular diseases and vascular malformations of the nervous system ; Vasodilator agents. Cerebral vasodilators</subject><ispartof>Dementia and geriatric cognitive disorders, 2005-01, Vol.19 (4), p.189-195</ispartof><rights>2005 S. Karger AG, Basel</rights><rights>2005 INIST-CNRS</rights><rights>Copyright 2005 S. Karger AG, Basel.</rights><rights>Copyright (c) 2005 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-3a5e750a388747c782df5a4c92a9874edfeb312b966d298283af094ec2fd9f393</citedby><cites>FETCH-LOGICAL-c418t-3a5e750a388747c782df5a4c92a9874edfeb312b966d298283af094ec2fd9f393</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,2423,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=16604048$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15677866$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>López-Pousa, S.</creatorcontrib><creatorcontrib>Turon-Estrada, A.</creatorcontrib><creatorcontrib>Garre-Olmo, J.</creatorcontrib><creatorcontrib>Pericot-Nierga, I.</creatorcontrib><creatorcontrib>Lozano-Gallego, M.</creatorcontrib><creatorcontrib>Vilalta-Franch, M.</creatorcontrib><creatorcontrib>Hernández-Ferràndiz, M.</creatorcontrib><creatorcontrib>Morante-Muñoz, V.</creatorcontrib><creatorcontrib>Isern-Vila, A.</creatorcontrib><creatorcontrib>Gelada-Batlle, E.</creatorcontrib><creatorcontrib>Majó-Llopart, J.</creatorcontrib><title>Differential Efficacy of Treatment with Acetylcholinesterase Inhibitors in Patients with Mild and Moderate Alzheimer’s Disease over a 6-Month Period</title><title>Dementia and geriatric cognitive disorders</title><addtitle>Dement Geriatr Cogn Disord</addtitle><description>There are various anticholinesterase inhibitors (AChEIs) for the symptomatic treatment of mild to moderate Alzheimer’s disease (AD). All AChEIs have shown greater efficacy than placebo in randomized, double-blind, parallel-group clinical trials. No differential studies have yet been made of the efficacy between all AChEIs. The study aims to determine the differential efficacy of the AChEIs with respect to a historical sample of patients with AD that were not treated with AChEIs. An open-label, prospective, observational study with a retrospective control group was undertaken to examine the evolution of the cognitive function over a 6-month period. The patients were assessed with the Mini-Mental State Examination (MMSE) at study entry and at 6 months. A general linear model was applied for repeated measurements with the MMSE score as the dependent variable, treatment type as an independent variable and the severity of the deterioration, age and the MMSE baseline score as covariables. Of the sample of 147 patients, 40 initiated treatment with donepezil, 32 with galantamine, 30 with rivastigmine and 45 were part of a historical sample of the memory clinic patients between 1991 and 1996 that had not been treated with AChEIs. The average age was 73.7 years (SD = 6.9; range = 52–86), 67.3% were women, 78.2% of the cases were mild and the MMSE baseline score was 18.1 points (range = 11–27). No significant intergroup differences were observed in these variables. The average doses of donepezil, galantamine and rivastigmine were 5.87 mg/day (SD = 1.92), 14.81 mg/day (SD = 6.25) and 6.41 mg/day (SD = 1.82), respectively. At 6 months, the difference in the MMSE score with respect to the untreated group was 1.6 points for donepezil (95% CI 0.79–2.37; p < 0.001), 0.99 points for galantamine (95% CI 0.14–1.85; p = 0.01) and 0.90 points for rivastigmine (95% CI 0.05–1.74; p = 0.03). No significant differences were observed in the efficacy among the groups treated with AChEIs (p > 0.05). Treatment with AChEIs significantly delays the global cognitive impairment associated with AD for at least 6 months. Our study found no significant differences in efficacy between donepezil, galantamine and rivastigmine. Further studies in the context of daily clinical practice will determine the clinical significance of the changes observed. An important variability of the response to the treatment was observed in treated patients.</description><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimer Disease - diagnosis</subject><subject>Alzheimer Disease - drug therapy</subject><subject>Biological and medical sciences</subject><subject>Cardiovascular system</subject><subject>Cholinesterase Inhibitors - administration & dosage</subject><subject>Cholinesterase Inhibitors - therapeutic use</subject><subject>Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases</subject><subject>Drug Administration Schedule</subject><subject>Female</subject><subject>Galantamine - administration & dosage</subject><subject>Galantamine - therapeutic use</subject><subject>Humans</subject><subject>Indans - administration & dosage</subject><subject>Indans - therapeutic use</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Neuropsychological Tests</subject><subject>Original Research Article</subject><subject>Pharmacology. Drug treatments</subject><subject>Phenylcarbamates - administration & dosage</subject><subject>Phenylcarbamates - therapeutic use</subject><subject>Piperidines - administration & dosage</subject><subject>Piperidines - therapeutic use</subject><subject>Prospective Studies</subject><subject>Retrospective Studies</subject><subject>Rivastigmine</subject><subject>Severity of Illness Index</subject><subject>Time Factors</subject><subject>Vascular diseases and vascular malformations of the nervous system</subject><subject>Vasodilator agents. 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Leukodystrophies. Prion diseases</topic><topic>Drug Administration Schedule</topic><topic>Female</topic><topic>Galantamine - administration & dosage</topic><topic>Galantamine - therapeutic use</topic><topic>Humans</topic><topic>Indans - administration & dosage</topic><topic>Indans - therapeutic use</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Neuropsychological Tests</topic><topic>Original Research Article</topic><topic>Pharmacology. Drug treatments</topic><topic>Phenylcarbamates - administration & dosage</topic><topic>Phenylcarbamates - therapeutic use</topic><topic>Piperidines - administration & dosage</topic><topic>Piperidines - therapeutic use</topic><topic>Prospective Studies</topic><topic>Retrospective Studies</topic><topic>Rivastigmine</topic><topic>Severity of Illness Index</topic><topic>Time Factors</topic><topic>Vascular diseases and vascular malformations of the nervous system</topic><topic>Vasodilator agents. Cerebral vasodilators</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>López-Pousa, S.</creatorcontrib><creatorcontrib>Turon-Estrada, A.</creatorcontrib><creatorcontrib>Garre-Olmo, J.</creatorcontrib><creatorcontrib>Pericot-Nierga, I.</creatorcontrib><creatorcontrib>Lozano-Gallego, M.</creatorcontrib><creatorcontrib>Vilalta-Franch, M.</creatorcontrib><creatorcontrib>Hernández-Ferràndiz, M.</creatorcontrib><creatorcontrib>Morante-Muñoz, V.</creatorcontrib><creatorcontrib>Isern-Vila, A.</creatorcontrib><creatorcontrib>Gelada-Batlle, E.</creatorcontrib><creatorcontrib>Majó-Llopart, J.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Social Sciences Premium Collection</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Science Database (Alumni Edition)</collection><collection>Social Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Social Science Premium Collection</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest Psychology</collection><collection>Science Database</collection><collection>Social Science Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Dementia and geriatric cognitive disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>López-Pousa, S.</au><au>Turon-Estrada, A.</au><au>Garre-Olmo, J.</au><au>Pericot-Nierga, I.</au><au>Lozano-Gallego, M.</au><au>Vilalta-Franch, M.</au><au>Hernández-Ferràndiz, M.</au><au>Morante-Muñoz, V.</au><au>Isern-Vila, A.</au><au>Gelada-Batlle, E.</au><au>Majó-Llopart, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Differential Efficacy of Treatment with Acetylcholinesterase Inhibitors in Patients with Mild and Moderate Alzheimer’s Disease over a 6-Month Period</atitle><jtitle>Dementia and geriatric cognitive disorders</jtitle><addtitle>Dement Geriatr Cogn Disord</addtitle><date>2005-01-01</date><risdate>2005</risdate><volume>19</volume><issue>4</issue><spage>189</spage><epage>195</epage><pages>189-195</pages><issn>1420-8008</issn><eissn>1421-9824</eissn><coden>DGCDFX</coden><abstract>There are various anticholinesterase inhibitors (AChEIs) for the symptomatic treatment of mild to moderate Alzheimer’s disease (AD). All AChEIs have shown greater efficacy than placebo in randomized, double-blind, parallel-group clinical trials. No differential studies have yet been made of the efficacy between all AChEIs. The study aims to determine the differential efficacy of the AChEIs with respect to a historical sample of patients with AD that were not treated with AChEIs. An open-label, prospective, observational study with a retrospective control group was undertaken to examine the evolution of the cognitive function over a 6-month period. The patients were assessed with the Mini-Mental State Examination (MMSE) at study entry and at 6 months. A general linear model was applied for repeated measurements with the MMSE score as the dependent variable, treatment type as an independent variable and the severity of the deterioration, age and the MMSE baseline score as covariables. Of the sample of 147 patients, 40 initiated treatment with donepezil, 32 with galantamine, 30 with rivastigmine and 45 were part of a historical sample of the memory clinic patients between 1991 and 1996 that had not been treated with AChEIs. The average age was 73.7 years (SD = 6.9; range = 52–86), 67.3% were women, 78.2% of the cases were mild and the MMSE baseline score was 18.1 points (range = 11–27). No significant intergroup differences were observed in these variables. The average doses of donepezil, galantamine and rivastigmine were 5.87 mg/day (SD = 1.92), 14.81 mg/day (SD = 6.25) and 6.41 mg/day (SD = 1.82), respectively. At 6 months, the difference in the MMSE score with respect to the untreated group was 1.6 points for donepezil (95% CI 0.79–2.37; p < 0.001), 0.99 points for galantamine (95% CI 0.14–1.85; p = 0.01) and 0.90 points for rivastigmine (95% CI 0.05–1.74; p = 0.03). No significant differences were observed in the efficacy among the groups treated with AChEIs (p > 0.05). Treatment with AChEIs significantly delays the global cognitive impairment associated with AD for at least 6 months. Our study found no significant differences in efficacy between donepezil, galantamine and rivastigmine. Further studies in the context of daily clinical practice will determine the clinical significance of the changes observed. An important variability of the response to the treatment was observed in treated patients.</abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>15677866</pmid><doi>10.1159/000083498</doi><tpages>7</tpages></addata></record> |
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recordid | cdi_proquest_journals_232497514 |
source | MEDLINE; Karger Journals |
subjects | Aged Aged, 80 and over Alzheimer Disease - diagnosis Alzheimer Disease - drug therapy Biological and medical sciences Cardiovascular system Cholinesterase Inhibitors - administration & dosage Cholinesterase Inhibitors - therapeutic use Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Drug Administration Schedule Female Galantamine - administration & dosage Galantamine - therapeutic use Humans Indans - administration & dosage Indans - therapeutic use Male Medical sciences Middle Aged Neurology Neuropsychological Tests Original Research Article Pharmacology. Drug treatments Phenylcarbamates - administration & dosage Phenylcarbamates - therapeutic use Piperidines - administration & dosage Piperidines - therapeutic use Prospective Studies Retrospective Studies Rivastigmine Severity of Illness Index Time Factors Vascular diseases and vascular malformations of the nervous system Vasodilator agents. Cerebral vasodilators |
title | Differential Efficacy of Treatment with Acetylcholinesterase Inhibitors in Patients with Mild and Moderate Alzheimer’s Disease over a 6-Month Period |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T16%3A12%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pasca&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Differential%20Efficacy%20of%20Treatment%20with%20Acetylcholinesterase%20Inhibitors%20in%20Patients%20with%20Mild%20and%20Moderate%20Alzheimer%E2%80%99s%20Disease%20over%20a%206-Month%20Period&rft.jtitle=Dementia%20and%20geriatric%20cognitive%20disorders&rft.au=L%C3%B3pez-Pousa,%20S.&rft.date=2005-01-01&rft.volume=19&rft.issue=4&rft.spage=189&rft.epage=195&rft.pages=189-195&rft.issn=1420-8008&rft.eissn=1421-9824&rft.coden=DGCDFX&rft_id=info:doi/10.1159/000083498&rft_dat=%3Cproquest_pasca%3E20688808%3C/proquest_pasca%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=232497514&rft_id=info:pmid/15677866&rfr_iscdi=true |