Evidence map›Paper›PMID 35328553›Full record

ReviewInternational journal of molecular sciences2022

Specialized Proresolving Lipid Mediators: A Potential Therapeutic Target for Atherosclerosis.

Juan Salazar, Daniela Pirela, Manuel Nava, Ana Castro, Lissé Angarita, Heliana Parra, Samuel Durán-Agüero, Diana Marcela Rojas-Gómez, Néstor Galbán, Roberto Añez and 5 more

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Lipid metabolism, microglia, and stroke.Neural regeneration research · 2026
    Article
  5. Review
  6. Review
  7. Review
  8. Review
  9. Review
  10. Article
  11. Resolvin D2/GPR18 signaling enhances monocytic myeloid-derived suppressor cell function to mitigate abdominal aortic aneurysm formation.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
  12. Review
  13. Omega-3 (Nutrients · 2024
    Review
  14. Article
  15. Review
  16. Review
  17. Review
  18. Molecular Pharmacology of Inflammation Resolution in Atherosclerosis.International 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

15 authors.

Juan SalazarEndocrine and Metabolic Diseases Research Center "DR. Felix Gomez", School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.ORCID 0000-0003-4211-528X
Daniela PirelaEndocrine and Metabolic Diseases Research Center "DR. Felix Gomez", School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.
Manuel NavaEndocrine and Metabolic Diseases Research Center "DR. Felix Gomez", School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.ORCID 0000-0001-9769-1693
Ana CastroEndocrine and Metabolic Diseases Research Center "DR. Felix Gomez", School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.
Lissé AngaritaEscuela de Nutrición y Dietética, Facultad de Medicina, Universidad Andres Bello, Concepción 4260000, Chile.ORCID 0000-0001-7860-5112
Heliana ParraEndocrine and Metabolic Diseases Research Center "DR. Felix Gomez", School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.ORCID 0000-0002-6604-4212
Samuel Durán-AgüeroFacultad de Ciencias para el Cuidado de la Salud, Universidad de San Sebastián, Lota 2465, Providencia, Santiago 7500000, Chile.ORCID 0000-0002-0548-3676
Diana Marcela Rojas-GómezEscuela de Nutrición y Dietética, Facultad de Medicina, Universidad Andres Bello, Santiago 8370321, Chile.ORCID 0000-0002-6956-6315
Néstor GalbánEndocrine and Metabolic Diseases Research Center "DR. Felix Gomez", School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.
Roberto AñezDepartamento de Endocrinología y Nutrición, Hospital General Universitario Gregorio Marañón, 28009 Madrid, Spain.
Maricarmen ChacínFacultad de Ciencias de la Salud, Universidad Simón Bolívar, Barranquilla 080002, Colombia.
Andrea DiazEndocrine and Metabolic Diseases Research Center "DR. Felix Gomez", School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.
Nelson VillasmilEndocrine and Metabolic Diseases Research Center "DR. Felix Gomez", School of Medicine, University of Zulia, Maracaibo 4001, Venezuela.ORCID 0000-0002-7227-4866
Juan Bautista De SanctisInstitute of Molecular and Translational Medicine, Czech Advanced Technology and Research Institute, Palacký University, Hněvotínská 1333/5, 779 00 Olomouc, Czech Republic.ORCID 0000-0002-5480-4608
Valmore BermúdezFacultad de Ciencias de la Salud, Universidad Simón Bolívar, Barranquilla 080002, Colombia.ORCID 0000-0003-1880-8887

Funding

Consejo de Desarrollo Científico, Humanístico y Tecnológico (CONDES), University of Zulia CC-0437-10-21-09-10
6 · The paper itself

Abstract

Cardiovascular disease (CVD) is a global public health issue due to its high morbidity, mortality, and economic impact. The implementation of innovative therapeutic alternatives for CVD is urgently required. Specialized proresolving lipid mediators (SPMs) are bioactive compounds derived from ω-3 and ω-6 fatty acids, integrated into four families: Lipoxins, Resolvins, Protectins, and Maresins. SPMs have generated interest in recent years due to their ability to promote the resolution of inflammation associated with the pathogeneses of numerous illnesses, particularly CVD. Several preclinical studies in animal models have evidenced their ability to decrease the progression of atherosclerosis, intimal hyperplasia, and reperfusion injury via diverse mechanisms. Large-scale clinical trials are required to determine the effects of SPMs in humans. This review integrates the currently available knowledge of the therapeutic impact of SPMs in CVD from preclinical and clinical studies, along with the implicated molecular pathways. In vitro results have been promising, and as such, SPMs could soon represent a new therapeutic alternative for CVD.

Indexed as

AtherosclerosisCardiovascular DiseasesFatty Acids, Omega-3AnimalsDocosahexaenoic AcidsHumansInflammationInflammation MediatorsDocosahexaenoic AcidsFatty Acids, Omega-3Inflammation Mediatorsatherosclerosisinflammationintimal hyperplasiareperfusion injuryresolutionspecialized proresolving mediators

Identifiers

PMID35328553
PMCPMC8955102

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.