Evidence map›Paper›PMID 26467378›Full record

ArticleAnatolian journal of cardiology2016

The association of paraoxonase 1 gene L55M polymorphism with the extent and severity of coronary artery disease in the Turkish population and its dependence on gender.

Derya Beyza Sayın Kocakap, Mehmet Tolga Doğru, Vedat Şimşek, Feryal Çabuk, Nesligül Yıldırım, Yunus Çelik, Sibel Alyılmaz Bekmez, Solmaz Erdem

Open access · diamondAbstract read
In one paragraph

Article in Anatolian journal of cardiology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. International journal of clinical and experimental pathology · 2018
    Article
  7. Article
  8. Relationship between rs854560Disease markers · 2017
    Article
  9. Article
  10. Article
  11. Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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

8 authors at 1 institution in 1 country.

Derya Beyza Sayın KocakapDepartment of Medical Genetics, Faculty of Medicine, Kırıkkale University; Kırıkkale-Turkey. dsayin@yahoo.com.
Mehmet Tolga Doğru
Vedat Şimşek
Feryal Çabuk
Nesligül Yıldırım
Yunus Çelik
Sibel Alyılmaz Bekmez
Solmaz Erdem
Yahoo (Spain) · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveCoronary artery disease (CAD) is a common, complex, and progressive disorder characterized by the accumulation of lipids and fibrous elements in the arteries. It is one of the leading causes of death in industrialized nations. Oxidative modification of low-density lipoprotein (LDL) in the arterial wall plays an important role in the initiation and progression of atherosclerosis. Paraoxonase1 (PON1) is involved in lipid metabolism and is believed to protect LDL oxidation. In our study, we aimed to clarify the relationship between PON1 gene L55M polymorphism and the extent and severity of CAD.

methodsIn total, 114 patients (54 males, mean age: 56.7 ± 12.0 years; 60 females, mean age: 55.7 ± 13.2 years) with stable angina or angina equivalent symptoms were enrolled in this prospective study. Cardiological evaluation was performed with electrocardiogram and transthoracic echocardiogram. The presence of hypertension, dyslipidemia, diabetes, and smoking status were ascertained. The patients were grouped according to their Gensini scores and gender. Genetic analysis of the PON1 gene L55M polymorphism was performed by polymerase chain reaction-restriction fragment length polymorphism.

resultsWe determined that the LL genotype was more prevalent in patients with Gensini score higher than or equal to 20 (p=0.026) and that this correlated with severe atherosclerotic coronary artery lesions in both gender groups, reaching a statistical significance in the female subjects (p=0.038).

conclusionIt was thought that the PON1 gene L55M polymorphism plays a significant role in CAD progression, especially in females.

Indexed as

AryldialkylphosphataseCoronary Artery DiseaseElectrocardiographyFemaleGenetic Predisposition to DiseaseHumansMaleMiddle AgedPolymorphism, GeneticProspective StudiesRisk FactorsSeverity of Illness IndexSex FactorsTurkeyWhite PeopleAryldialkylphosphatasePON1 protein, human

Identifiers

PMID26467378
PMCPMC5336803
OpenAlexW2396385885

What OpenQuestion holds

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LicenceCC BY-NC-SA
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Registered trials

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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.