Evidence map›Paper›PMID 29254093›Full record

ReviewJournal of Alzheimer's disease : JAD2018

Memantine for the Treatment of Dementia: A Review on its Current and Future Applications.

Jaume Folch, Oriol Busquets, Miren Ettcheto, Elena Sánchez-López, Ruben Dario Castro-Torres, Ester Verdaguer, Maria Luisa Garcia, Jordi Olloquequi, Gemma Casadesús, Carlos Beas-Zarate and 4 more

2 registry-linked trialsOpen access · bronzeAbstract readReview
In one paragraph

Review in Journal of Alzheimer's disease : JAD, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 123 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
123citing papers in PubMed, 4 pooled it
9.6field-weighted citation impact, top 1% 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.

NCT06417034 nacompletednot on this mapstarted 2022, after this paper: background citation

Hand Training Device For Cognitive Care

TypeinterventionalSponsorNational Cheng-Kung University HospitalRan2022 to 2022Enrolled80ConditionsHealthy Elderly, Mild Cognitive Impairment (MCI)ArmsGame Software
NCT06679387 phase2recruitingnot on this mapstarted 2024, after this paper: background citation

"The Effect of Memantine on the Prevention and Amelioration of Paclitaxel-induced Toxicity in Breast Cancer Patients"

TypeinterventionalSponsorAin Shams UniversityRan2024 to 2025Enrolled80ConditionsBreast Cancer Early Stage Breast Cancer (Stage 1-3)ArmsMemantine-HCl, Placebo Oral Tablet
3 · Its place in the literature

Who cites it

123 citing papers in PubMed, 4 syntheses or guidelines pooled it, 236 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Pooled it
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. A Study of 3-Substituted 7-Methoxy-2,3,4,5-tetrahydro-1Molecules (Basel, Switzerland) · 2026
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

63 more citing papers are in PubMed but not listed here.

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

14 authors at 5 institutions in 4 countries.

Jaume FolchDepartament de Bioquímica, Facultat de Medicina i Ciències de la Salut, Universitat Rovira i Virgili, Reus, Spain.
Oriol BusquetsDepartament de Farmacologia, Toxicologia i Química Terapèutica, Facultat de Farmàcia i Ciències de l'Alimentació, Universitat de Barcelona, Barcelona, Spain.
Miren EttchetoDepartament de Farmacologia, Toxicologia i Química Terapèutica, Facultat de Farmàcia i Ciències de l'Alimentació, Universitat de Barcelona, Barcelona, Spain.
Elena Sánchez-LópezBiomedical Research Networking Centre in Neurodegenerative Diseases (CIBERNED), Madrid, Spain.
Ruben Dario Castro-TorresDepartament de Farmacologia, Toxicologia i Química Terapèutica, Facultat de Farmàcia i Ciències de l'Alimentació, Universitat de Barcelona, Barcelona, Spain.
Ester VerdaguerDepartament de Farmacologia, Toxicologia i Química Terapèutica, Facultat de Farmàcia i Ciències de l'Alimentació, Universitat de Barcelona, Barcelona, Spain.
Maria Luisa GarciaUnitat de Farmàcia, Tecnologia Farmacèutica i Fisico-química, Facultat de Farmàcia i Ciències de l'Alimentació, Universitat de Barcelona, Barcelona, Spain.
Jordi OlloquequiInstituto de Ciencias Biomédicas, Facultad de Ciencias de la Salud, Universidad Autónoma de Chile, Talca, Chile.
Gemma CasadesúsDepartment of Biological Sciences, Kent State University, Kent, OH, USA.
Carlos Beas-ZarateDepartamento de Biología Celular y Molecular, Laboratorio de Regeneración y Desarrollo Neural, Instituto de Neurobiología, CUCBA, México.
Carme PelegriBiomedical Research Networking Centre in Neurodegenerative Diseases (CIBERNED), Madrid, Spain.
Jordi VilaplanaBiomedical Research Networking Centre in Neurodegenerative Diseases (CIBERNED), Madrid, Spain.
Carme AuladellBiomedical Research Networking Centre in Neurodegenerative Diseases (CIBERNED), Madrid, Spain.
Antoni CaminsDepartament de Farmacologia, Toxicologia i Química Terapèutica, Facultat de Farmàcia i Ciències de l'Alimentació, Universitat de Barcelona, Barcelona, Spain.
Biomedical Research Networking Center on Neurodegenerative Diseases · ESInstitut de Nanociència i Nanotecnologia de la Universitat de BarcelonaInstituto de Neurologia Y Neurocirugia · CUKent State University · USUniversidad Autónoma de Chile · CL

Funding

Mechanisms of Metabolic Hormone Amylin Action on Alzheimer's Disease PathogenesisR15AG050292 · NIA · KENT STATE UNIVERSITY · PI CASADESUS, GEMMA · 2016 to 2016
$444k
NIA NIH HHS R15 AG050292
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder characterized by the presence in the brain of extracellular amyloid-β protein (Aβ) and intracellular neurofibrillary tangles composed of hyperphosphorylated tau protein. The N-Methyl-D-aspartate receptors (NMDAR), ionotropic glutamate receptor, are essential for processes like learning and memory. An excessive activation of NMDARs has been associated with neuronal loss. The discovery of extrasynaptic NMDARs provided a rational and physiological explanation between physiological and excitotoxic actions of glutamate. Memantine (MEM), an antagonist of extrasynaptic NMDAR, is currently used for the treatment of AD jointly with acetylcholinesterase inhibitors. It has been demonstrated that MEM preferentially prevents the excessive continuous extrasynaptic NMDAR disease activation and therefore prevents neuronal cell death induced by excitotoxicity without disrupting physiological synaptic activity. The problem is that MEM has shown no clear positive effects in clinical applications while, in preclinical stages, had very promising results. The data in preclinical studies suggests that MEM has a positive impact on improving AD brain neuropathology, as well as in preventing Aβ production, aggregation, or downstream neurotoxic consequences, in part through the blockade of extrasynaptic NMDAR. Thus, the focus of this review is primarily to discuss the efficacy of MEM in preclinical models of AD, consider possible combinations of this drug with others, and then evaluate possible reasons for its lack of efficacy in clinical trials. Finally, applications in other pathologies are also considered.

Indexed as

Alzheimer DiseaseAnimalsHumansMemantineNeuroprotective AgentsMemantineNeuroprotective AgentsAlzheimer’s diseaseamyloid β-proteinextrasynaptic N-Methyl-D-aspartate receptormemantinetau protein

Identifiers

PMID29254093
PMCPMC5870028
OpenAlexW2775709378

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.