Evidence map›Paper›PMID 38069339›Full record

ReviewInternational journal of molecular sciences2023

PDE4 Phosphodiesterases in Cardiovascular Diseases: Key Pathophysiological Players and Potential Therapeutic Targets.

Lídia Puertas-Umbert, Judith Alonso, Leif Hove-Madsen, José Martínez-González, Cristina Rodríguez

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Phosphodiesterases: Evolving Concepts and Implications for Human Therapeutics.Annual review of pharmacology and toxicology · 2025
    Review
  8. Article
  9. Article
  10. Emerging Anti-Inflammatory COPD Treatments: Potential Cardiovascular Impacts.International journal of chronic obstructive pulmonary disease · 2024
    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

5 authors at 2 institutions in 1 country.

Lídia Puertas-UmbertInstitut de Recerca Sant Pau (IR SANT PAU), 08041 Barcelona, Spain.
Judith AlonsoInstitut de Recerca Sant Pau (IR SANT PAU), 08041 Barcelona, Spain.
Leif Hove-MadsenInstitut de Recerca Sant Pau (IR SANT PAU), 08041 Barcelona, Spain.ORCID 0000-0001-5493-3998
José Martínez-GonzálezInstitut de Recerca Sant Pau (IR SANT PAU), 08041 Barcelona, Spain.ORCID 0000-0002-3894-7166
Cristina RodríguezInstitut de Recerca Sant Pau (IR SANT PAU), 08041 Barcelona, Spain.ORCID 0000-0002-6472-5647
Consejo Superior de Investigaciones Científicas · ESInstituto de Salud Carlos III · ES

Funding

Fundación Española de Arteriosclerosis FEA 2020Instituto de Salud Carlos III PI21/01048Ministerio de Ciencia e Innovación PID2021-122509OB-I00
6 · The paper itself

Abstract

3',5'-cyclic adenosine monophosphate (cAMP) is a second messenger critically involved in the control of a myriad of processes with significant implications for vascular and cardiac cell function. The temporal and spatial compartmentalization of cAMP is governed by the activity of phosphodiesterases (PDEs), a superfamily of enzymes responsible for the hydrolysis of cyclic nucleotides. Through the fine-tuning of cAMP signaling, PDE4 enzymes could play an important role in cardiac hypertrophy and arrhythmogenesis, while it decisively influences vascular homeostasis through the control of vascular smooth muscle cell proliferation, migration, differentiation and contraction, as well as regulating endothelial permeability, angiogenesis, monocyte/macrophage activation and cardiomyocyte function. This review summarizes the current knowledge and recent advances in understanding the contribution of the PDE4 subfamily to cardiovascular function and underscores the intricate challenges associated with targeting PDE4 enzymes as a therapeutic strategy for the management of cardiovascular diseases.

Indexed as

Cardiovascular DiseasesCyclic Nucleotide Phosphodiesterases, Type 43',5'-Cyclic-AMP PhosphodiesterasesCyclic AMPHumansMyocytes, CardiacSecond Messenger Systems3',5'-Cyclic-AMP PhosphodiesterasesCyclic AMPCyclic Nucleotide Phosphodiesterases, Type 4cardiovascular diseasesPDE4therapy

Identifiers

PMID38069339
PMCPMC10707411
OpenAlexW4389242567

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.