Evidence map›Paper›PMID 32380022›Full record

ReviewNeuropharmacology2020

Opportunities for multiscale computational modelling of serotonergic drug effects in Alzheimer's disease.

Alok Joshi, Da-Hui Wang, Steven Watterson, Paula L McClean, Chandan K Behera, Trevor Sharp, KongFatt Wong-Lin

Open access · hybridAbstract readReview
In one paragraph

Review in Neuropharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Neurotransmitters in Prevention and Treatment of Alzheimer's Disease.International journal of molecular sciences · 2023
    Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
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

7 authors at 3 institutions in 2 countries.

Alok JoshiIntelligent Systems Research Centre, Ulster University, Derry~Londonderry, Northern Ireland, UK. Electronic address: a.joshi@ulster.ac.uk.
Da-Hui WangState Key Laboratory of Cognitive Neuroscience and Learning, Beijing Normal University, Beijing, China; School of System Science, Beijing Normal University, Beijing, China.
Steven WattersonNorthern Ireland Centre for Stratified Medicine, Biomedical Sciences Research Institute, Ulster University, Derry~Londonderry, Northern Ireland, UK.
Paula L McCleanNorthern Ireland Centre for Stratified Medicine, Biomedical Sciences Research Institute, Ulster University, Derry~Londonderry, Northern Ireland, UK.
Chandan K BeheraIntelligent Systems Research Centre, Ulster University, Derry~Londonderry, Northern Ireland, UK.
Trevor SharpDepartment of Pharmacology, University of Oxford, Oxford, UK.
KongFatt Wong-LinIntelligent Systems Research Centre, Ulster University, Derry~Londonderry, Northern Ireland, UK. Electronic address: k.wong-lin@ulster.ac.uk.
University of Ulster · GBBeijing Normal University · CNUniversity of Oxford · GB

Funding

Biotechnology and Biological Sciences Research Council BB/P003427/1
6 · The paper itself

Abstract

Alzheimer's disease (AD) is an age-specific neurodegenerative disease that compromises cognitive functioning and impacts the quality of life of an individual. Pathologically, AD is characterised by abnormal accumulation of beta-amyloid (Aβ) and hyperphosphorylated tau protein. Despite research advances over the last few decades, there is currently still no cure for AD. Although, medications are available to control some behavioural symptoms and slow the disease's progression, most prescribed medications are based on cholinesterase inhibitors. Over the last decade, there has been increased attention towards novel drugs, targeting alternative neurotransmitter pathways, particularly those targeting serotonergic (5-HT) system. In this review, we focused on 5-HT receptor (5-HTR) mediated signalling and drugs that target these receptors. These pathways regulate key proteins and kinases such as GSK-3 that are associated with abnormal levels of Aβ and tau in AD. We then review computational studies related to 5-HT signalling pathways with the potential for providing deeper understanding of AD pathologies. In particular, we suggest that multiscale and multilevel modelling approaches could potentially provide new insights into AD mechanisms, and towards discovering novel 5-HTR based therapeutic targets.

Indexed as

Patient-Specific ModelingAlzheimer DiseaseAnimalsHumansReceptors, SerotoninSerotonin AgentsTreatment OutcomeReceptors, SerotoninSerotonin AgentsAlzheimer's diseaseBeta-amyloidBoolean modelsData-driven modelsDementiaGSK-3Knowledge-driven modelsMechanistic modelsMultiscale computational modellingSerotoninSerotonin targeted drugsTau

Identifiers

PMID32380022
PMCPMC7322519
OpenAlexW3023504426

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.