Evidence map›Paper›PMID 36118876›Full record

ReviewFrontiers in genetics2022

Paraoxonase 1 gene polymorphisms in lipid oxidation and atherosclerosis development.

Marija Vavlukis, Ana Vavlukis, Katerina Krsteva, Sonja Topuzovska

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in genetics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

  1. Association ofPakistan journal of medical sciences · 2026
    Article
  2. Article
  3. Article
  4. The Impact of Genetic Factors in Ménière's Disease.International journal of molecular sciences · 2026
    Review
  5. Observational
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  8. Review
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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.

Marija VavlukisUniversity Clinic for Cardiology, Skopje, North Macedonia.
Ana VavlukisFaculty of Pharmacy, Ss. Cyril and Methodius University in Skopje, Skopje, North Macedonia.
Katerina KrstevaFaculty of Pharmacy, Ss. Cyril and Methodius University in Skopje, Skopje, North Macedonia.
Sonja TopuzovskaInstitute of Medical and Experimental Biochemistry, Faculty of Medicine, Ss. Cyril and Methodius University in Skopje, Skopje, North Macedonia.
Saints Cyril and Methodius University of Skopje · MKPHI University Psychiatric Clinic - Skopje · MK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paraoxonase 1 (PON1) is calcium-dependent aryldialkylphosphatase, thought to possess; anti-oxidant, anti-adhesion, anti-inflammatory, anti-thrombosis and anti-apoptosis effects, as well as lipid-modifying properties. Numerous clinical studies have shown associations between different PON1 polymorphisms and different cardiovascular pathologies. The rs622 (c.575A > G) and the rs854560 (c.163A > T) are the most studied PON1 SNPs in the coding region, with rs705381 (- 162A/G), rs854572 (- 909G/C) and rs705379 (- 108C/T) being the most studied SNPs in the regulatory PON1 gene region. The three major PON1 activities are aryldialkylphosphatase, arylesterase and lactonase activity. The different SNPs affect PON1 serum concentrations and enzyme activity, thus leading to pro-/anti-atherogenic effects. In that setting, it is very difficult to establish as to whether the genotype or phenotype of PON1 is primarily associated with cardiovascular risk. Given the current scientific evidence, PON1 genotyping might be reasonable in patients with high and very high cardiovascular risk.

Indexed as

atherosclerosisenzyme activityHDL cholesterolparaoxonase 1polymorphism

Identifiers

PMID36118876
PMCPMC9478165
OpenAlexW4294176401

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.