Evidence map›Paper›PMID 34844537›Full record

ReviewCurrent medicinal chemistry2022

A

Stefania Merighi, Pier A Borea, Katia Varani, Fabrizio Vincenzi, Kenneth A Jacobson, Stefania Gessi

Open access · greenAbstract readReview
In one paragraph

Review in Current medicinal chemistry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.2field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 37 citations in OpenAlex.

  1. Applying Deep-Learning-DrivenJournal of medicinal chemistry · 2026
    Article
  2. Neoantigen mRNA vaccines and AHuman vaccines & immunotherapeutics · 2025
    Review
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Adenosine and adenosine receptors in metabolic imbalance-related neurological issues.Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie · 2024
    Review
  11. Article
  12. Review
  13. Adenosine ABiomolecules · 2023
    Article
  14. Dual Anta-Inhibitors Targeting Protein Kinase CK1δ and AMolecules (Basel, Switzerland) · 2023
    Article
  15. Review
  16. Crystal structure of adenosine ACommunications chemistry · 2023
    Article
  17. Review
  18. Chemobrain: An accelerated aging process linking adenosine AInternational review of neurobiology · 2023
    Review
  19. Review
  20. AInternational journal of molecular sciences · 2022
    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

6 authors at 2 institutions in 2 countries.

Stefania MerighiDepartment of Translational Medicine and for Romagna, University of Ferrara, 44121, Ferrara, Italy.
Pier A BoreaUniversity of Ferrara, 44121, Ferrara, Italy.
Katia VaraniDepartment of Translational Medicine and for Romagna, University of Ferrara, 44121, Ferrara, Italy.
Fabrizio VincenziDepartment of Translational Medicine and for Romagna, University of Ferrara, 44121, Ferrara, Italy.
Kenneth A JacobsonMolecular Recognition Section, Laboratory of Bioorganic Chemistry, National Institute of Diabetes and Digestive and Kidney Diseases, Bethesda, MD, USA.
Stefania GessiDepartment of Translational Medicine and for Romagna, University of Ferrara, 44121, Ferrara, Italy.
University of Ferrara · ITNational Institute of Diabetes and Digestive and Kidney Diseases · US

Funding

Development Of Drugs Acting At Adenosine ReceptorsZIADK031117 · NIDDK · NATIONAL INSTITUTE OF DIABETES AND DIGESTIVE AND KIDNEY DISEASES · PI JACOBSON, KENNETH ALAN · 2009 to 2025
$10.4M
Intramural NIH HHS ZIA DK031117NIDDK Intramural Research Program ZIADK031117
6 · The paper itself

Abstract

backgroundAlzheimer's disease (AD) is the most common form of dementia worldwide, with approximately 6 million cases reported in America in 2020. The clinical signs of AD include cognitive dysfunction, apathy, anxiety and neuropsychiatric signs, and pathogenetic mechanisms that involve amyloid peptide-β extracellular accumulation and tau hyperphosphorylation. Unfortunately, current drugs to treat AD can provide only symptomatic relief but are not disease-modifying molecules able to revert AD progression. The endogenous modulator adenosine, through A

objectiveIn this review, recent advances covering A

methodsHerein, the literature on A

resultsCaffeine, the most widely consumed natural product stimulant and an A

conclusionThis review highlights the clinical potential of A

Indexed as

Alzheimer DiseaseNeurodegenerative DiseasesAdenosine A2 Receptor AntagonistsAmyloid beta-PeptidesAnimalsCaffeineHumansPurinergic P1 Receptor AntagonistsReceptor, Adenosine A2AAdenosine A2 Receptor AntagonistsAmyloid beta-PeptidesCaffeinePurinergic P1 Receptor AntagonistsReceptor, Adenosine A2AAAlzheimer’s diseasecognitive impairmentdrug designneuroinflammation

Identifiers

PMID34844537
PMCPMC9148371
OpenAlexW3216825752

What OpenQuestion holds

Textmetadata
LicenceTDM
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.