Evidence map›Paper›PMID 25405733›Full record

SynthesisInternational journal of molecular sciences2014

Exploring the role of paraoxonases in the pathogenesis of coronary artery disease: a systematic review.

David Abelló, Elena Sancho, Jordi Camps, Jorge Joven

Open access · goldAbstract readSystematic Review
In one paragraph

Synthesis in International journal of molecular sciences, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 45 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Article
  9. The Role ofGlobal medical genetics · 2020
    Review
  10. Article
  11. Linc-OIP5 working as a ceRNA of miR-616 promotes PON1 expression in HUEVC cells.International journal of clinical and experimental pathology · 2020
    Article
  12. Article
  13. Mutual Influences between Nitric Oxide and Paraoxonase 1.Antioxidants (Basel, Switzerland) · 2019
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Oxidative Stress Genes, Antioxidants and Coronary Artery Disease in Type 2 Diabetes Mellitus.Cardiovascular & hematological agents in medicinal chemistry · 2016
    Review
  20. Article
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

4 authors at 2 institutions in 1 country.

David AbellóDepartment of Medicine and Surgery, Faculty of Medicine and Health Sciences, Rovira i Virgili University, C. Sant Llorenç, s/n, Reus, Catalonia 43201, Spain. davidabelloaudi@gmail.com.
Elena SanchoDepartment of Medicine and Surgery, Faculty of Medicine and Health Sciences, Rovira i Virgili University, C. Sant Llorenç, s/n, Reus, Catalonia 43201, Spain. sancho.08@hotmail.com.
Jordi CampsDepartment of Medicine and Surgery, Faculty of Medicine and Health Sciences, Rovira i Virgili University, C. Sant Llorenç, s/n, Reus, Catalonia 43201, Spain. jcamps@grupsagessa.com.
Jorge JovenDepartment of Medicine and Surgery, Faculty of Medicine and Health Sciences, Rovira i Virgili University, C. Sant Llorenç, s/n, Reus, Catalonia 43201, Spain. jorge.joven@urv.cat.
Institut de Recerca Biomèdica Catalunya Sud · ESUniversitat Rovira i Virgili · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paraoxonases (PON) are three enzymes (PON1, PON2 and PON3) that play a role in the organism's antioxidant system; alterations in which are associated with diseases involving oxidative stress. In this review, we summarize the evidence of PON related to the pathogenesis of coronary artery disease (CAD) and atherosclerosis. We searched three electronic databases (PubMed, Scopus and Cochrane Database) with no date limit. All of the articles selected investigated PON enzymatic activity and/or PON gene polymorphisms. The selection focused on PON in relation to atherosclerosis, CAD and myocardial infarction. The exclusion criteria were a sample size <100 patients, non-human studies, editorials and systematic reviews without restrictions on the country of origin. With these criteria, we identified thirty-five prospective studies published between 1986 and 2014 with a total of 28,164 participants. The relationship between PON gene polymorphisms and CAD was not conclusive, but most studies support the concept that alterations in PON1 enzymatic activity levels do influence atheroma formation. Conversely, relationships between PON2 and PON3 vs. CAD have not been extensively investigated. Our review of the current data concludes that the bases of paraoxonases involvement in atherosclerosis are poorly understood and that this issue requires future comprehensive, multi-centered studies.

Indexed as

AnimalsAryldialkylphosphataseAtherosclerosisCoronary Artery DiseaseCoronary VesselsHumansMyocardial InfarctionOxidative StressPolymorphism, GeneticAryldialkylphosphatasePON1 protein, humanPON2 protein, humanPON3 protein, human

Identifiers

PMID25405733
PMCPMC4264208
OpenAlexW2149998096

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.