Evidence map›Paper›PMID 23173065›Full record

ReviewACS chemical neuroscience2012

Phosphodiesterases as therapeutic targets for Alzheimer's disease.

Ana García-Osta, Mar Cuadrado-Tejedor, Carolina García-Barroso, Julen Oyarzábal, Rafael Franco

Registry-linked trialAbstract readReview
In one paragraph

Review in ACS chemical neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02835716 (Pre-Clinical Alzheimer's), which is not on this map. Cited by 100 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
100citing papers in PubMed, 1 pooled it
5.8field-weighted citation impact, top 3% 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.

NCT02835716 unknown statusnot on this mapstarted 2016, after this paper: background citation

Pre-Clinical Alzheimer's (ALZ) Diagnosis (PCD) = Optimum Outcomes (OO)

Typeobservational_patient_registrySponsorMillennium Magnetic Technologies, LLCRan2016 to 2020Enrolled150ConditionsAlzheimer DiseaseArmsroflumilast, ustekinumab
3 · Its place in the literature

Who cites it

100 citing papers in PubMed, 1 synthesis or guideline pooled it, 263 citations in OpenAlex.

  1. Pooled it
  2. The PASTIS trial: Testing tadalafil for possible use in vascular cognitive impairment.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2022
    Trial
  3. Trial
  4. Article
  5. Review
  6. Review
  7. Radiosynthesis and Preclinical Evaluation of a NovelACS medicinal chemistry letters · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Protective effect of PDE4B subtype-specific inhibition in an App knock-in mouse model for Alzheimer's disease.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
    Article
  20. Article

40 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

5 authors.

Ana García-OstaMolecular and Cell Neuropharmacology Laboratory, Neurosciences Division, CIMA (Centro de investigación Médica Aplicada), Avda Pio XII, Pamplona, Spain. agosta@unav.es
Mar Cuadrado-Tejedor
Carolina García-Barroso
Julen Oyarzábal
Rafael Franco

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is the most common form of dementia among the elderly. In AD patients, memory loss is accompanied by the formation of beta-amyloid plaques and the appearance of tau in a pathological form. Given the lack of effective treatments for AD, the development of new management strategies for these patients is critical. The continued failure to find effective therapies using molecules aimed at addressing the anti-beta amyloid pathology has led researchers to focus on other non-amyloid-based approaches to restore memory function. Promising non-amyloid related candidate targets include phosphosdiesterases (PDEs), and indeed, Rolipram, a specific PDE4 inhibitor, was the first compound found to effectively restore cognitive deficits in animal models of AD. More recently, PDE5 inhibitors have also been shown to effectively restore memory function. Accordingly, inhibitors of other members of the PDE family may also improve memory performance in AD and non-AD animal models. Hence, in this review, we will summarize the data supporting the use of PDE inhibitors as cognitive enhancers and we will discuss the possible mechanisms of action underlying these effects. We shall also adopt a medicinal chemistry perspective that leads us to propose the most promising PDE candidates on the basis of inhibitor selectivity, brain distribution, and mechanism of action.

Indexed as

Alzheimer DiseaseAnimalsCarrier ProteinsCognitionCREB-Binding ProteinDisease Models, AnimalHumansIntracellular Signaling Peptides and ProteinsMemoryMemory DisordersMiceNootropic AgentsPhosphodiesterase 4 InhibitorsPhosphoric Diester Hydrolasestau ProteinsCarrier ProteinsCREB-Binding Proteincyclic GMP-binding proteinIntracellular Signaling Peptides and ProteinsNootropic AgentsPhosphodiesterase 4 InhibitorsPhosphoric Diester Hydrolasestau Proteins

Identifiers

PMID23173065
PMCPMC3503343
OpenAlexW2196088104

What OpenQuestion holds

Textmetadata
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.