Evidence map›Paper›PMID 22659994›Full record

Trial reportThe journal of nutrition, health & aging2012

A combination of galantamine and memantine modifies cognitive function in subjects with amnestic MCI.

O Peters, D Lorenz, A Fesche, K Schmidtke, M Hüll, R Perneczky, E Rüther, H-J Möller, F Jessen, W Maier and 10 more

Open access · bronzeAbstract readComparative StudyMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in The journal of nutrition, health & aging, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 6 pooled it
3.1field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

30 citing papers in PubMed, 6 syntheses or guidelines pooled it, 52 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Memantine for dementia.The Cochrane database of systematic reviews · 2019
    Pooled it
  5. Efficacy and safety of cognitive enhancers for patients with mild cognitive impairment: a systematic review and meta-analysis.CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne · 2013
    Pooled it
  6. Cholinesterase inhibitors for mild cognitive impairment.The Cochrane database of systematic reviews · 2012
    Pooled it
  7. Trial
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  14. Strategies for the use of Ginkgo biloba extract, EGb 761CNS neuroscience & therapeutics · 2021
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 12 institutions in 2 countries.

O PetersDepartment of Psychiatry, Charité - Campus Benjamin Franklin, Berlin, Germany. oliver.peters@charite.de
D Lorenz
A Fesche
K Schmidtke
M Hüll
R Perneczky
E Rüther
H-J Möller
F Jessen
W Maier
J Kornhuber
H Jahn
C Luckhaus
H-J Gertz
J Schröder
J Pantel
S Teipel
S Wellek
L Frölich
I Heuser
Charité - Universitätsmedizin Berlin · DEGerman Center for Neurodegenerative Diseases · DEUniversity Medical Center Freiburg · DECentral Institute of Mental Health · DEGoethe University Frankfurt · DEHeidelberg University · DEHeinrich Heine University Düsseldorf · DELeipzig University · DELudwig-Maximilians-Universität München · DETechnical University of Munich · DEUniversität Hamburg · DEUniversity of Göttingen · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesMild cognitive impairment (MCI) is etiologically heterogeneous, and a substantial proportion of MCI subjects will develop different dementia disorders. One subtype of this syndrome, amnestic MCI, occurs preferentially but not exclusively in prodromal AD and is characterized by defined deficits of episodic memory. DESIGN, SETTING AND

participantsFor a 2-year, double-blinded, placebo-controlled study MCI patients, presenting with an amnestic syndrome but not necessarily based on presumed prodromal AD were randomized.

interventionPatients received (a) a combination of 16 mg galantamine plus 20 mg memantine, or (b) 16 mg galantamine alone or (c) placebo. MEASUREMENTS: The primary objective was to explore the differential impact of these interventions on the progression to dementia and on cognitive changes as measured by the ADAScog.

resultsAfter recruitment of 232 subjects, the trial was halted before reaching the planned sample size, because safety concerns arose in other studies with galantamine in MCI. This resulted in a variable treatment duration of 2-52 weeks. The statistical analysis plan was amended for studying cognitive effects of discontinuing the study medication, which was done separately for galantamine and memantine, and under double-blind conditions. There was one death, no unexpected severe adverse events, and no differences of severe adverse events between the treatment arms. The cognitive changes on the ADAScog were not different among the groups. Only for the subgroup of amnestic MCI with presumed AD etiology, a significant improvement of ADAScog score over placebo before the discontinuation of medication was observed, while amnestic MCI presumably due to other etiologies showed no cognitive changes with broad variation. Cognitive improvement was numerically larger in the combination treatment group than under galantamine alone. Patients who received placebo declined as expected. Discontinuation of galantamine, either as part of the combination regimen or as mono treatment, resulted in a transient decline of the ADAScog score in amnestic MCI of presumed AD etiology, while discontinuation of Memantine did not change the cognitive status.

conclusionIn an interrupted trial with amnestic MCI subjects the combination of galantamine plus memantine were generally well tolerated. In the subgroup of MCI subjects with presumed AD etiology, a cognitive benefit of a short-term combination treatment of galantamine plus memantine was observed, and cognitive decline occurred after discontinuation of galantamine.

Indexed as

AgedAlzheimer DiseaseAmnesiaCholinesterase InhibitorsCognitionCognitive DysfunctionCohort StudiesDementiaDisease ProgressionDouble-Blind MethodDrug Therapy, CombinationEarly Termination of Clinical TrialsFemaleGalantamineGermanyHumansCholinesterase InhibitorsGalantamineMemantineNootropic AgentsReceptors, N-Methyl-D-Aspartate

Identifiers

PMID22659994
PMCPMC12878552
OpenAlexW2065168181

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.