Evidence map›Paper›PMID 36416040›Full record

ArticleMolecular genetics & genomic medicine2023

Evaluation of rs1748195 ANGPTL3 gene polymorphism in patients with angiographic coronary artery disease compared to healthy individuals.

Nafise Afkhami, Malihe Aghasizadeh, Somayeh Ghiasi Hafezi, Reza Zare-Feyzabadi, Sara Saffar Soflaei, Mohammad Rashidmayvan, Arezoo Rastegarmoghadam-Ebrahimian, Khashayar Khanizadeh, Nilufar Safari, Gordon A Ferns and 3 more

Open access · goldAbstract readComparative Study
In one paragraph

Article in Molecular genetics & genomic medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
2.5field-weighted citation impact, top 9% 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

1 citing paper in PubMed, 15 citations in OpenAlex.

  1. 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

13 authors at 3 institutions in 2 countries.

Nafise AfkhamiDepartment of Biology, Mashhad Branch, Islamic Azad University, Mashhad, Iran.
Malihe AghasizadehStudent Research Committee, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Somayeh Ghiasi HafeziIranian UNESCO Center of Excellence for Human Nutrition, Mashhad University of Medical Sciences, Mashhad, Iran.
Reza Zare-FeyzabadiIranian UNESCO Center of Excellence for Human Nutrition, Mashhad University of Medical Sciences, Mashhad, Iran.
Sara Saffar SoflaeiIranian UNESCO Center of Excellence for Human Nutrition, Mashhad University of Medical Sciences, Mashhad, Iran.
Mohammad RashidmayvanDepartment of Nutrition, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Arezoo Rastegarmoghadam-EbrahimianDepartment of Nutrition Sciences, Varastegan Institute for Medical Sciences, Mashhad, Iran.
Khashayar KhanizadehDepartment of Nutrition Sciences, Varastegan Institute for Medical Sciences, Mashhad, Iran.
Nilufar SafariDepartment of Nutrition Sciences, Varastegan Institute for Medical Sciences, Mashhad, Iran.
Gordon A FernsBrighton & Sussex Medical School, Division of Medical Education, Sussex, UK.
Habibollah EsmailySocial Determinants of Health Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
Reza Assaran DarbanDepartment of Biology, Mashhad Branch, Islamic Azad University, Mashhad, Iran.
Majid Ghayour-MobarhanIranian UNESCO Center of Excellence for Human Nutrition, Mashhad University of Medical Sciences, Mashhad, Iran.ORCID 0000-0002-1081-6754
Mashhad University of Medical Sciences · IRIslamic Azad University, Mashhad · IRBrighton and Sussex Medical School · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

subjectThe Angiopoietin-like 3 (ANGPTL3) gene has been reported to be associated with cardiovascular risk. This study is designed to compare the genetic variant (rs1748195) of the ANGPTL3 gene and the presence of a coronary artery occlusion of >50% in Iranian nation.

methodIn this study, 184 patients underwent angiography and 317 healthy individuals were evaluated for polymorphism of rs1748195 the ANGPTL3 gene using Tetra-ARMs PCR. Coronary patients who experience angiography were categorized into two groups: 54 patients who had an angiography indication for the first time and coronary occlusion was <50% (Angio-) and 134 patients who formerly underwent coronary stent implanting at least 1 month before with coronary occlusion of ≥50% that again have an angiography indication (Angio+). In addition, individuals with angio+ are categorized in two groups: (1) non-in-stent restenosis (NISR); patient with a patent stent (N = 92). (2) in-stent restenosis (ISR); in-stent stenosis >50% (N = 42).

resultThe fundamental of characteristics of our study design population was categorized based on undergoing angiography or not. In the present study, we investigated that the CC genotype, and also the A allele corresponding to rs1748195 at the ANGPTL3 gene loci, was associated with negative angiogram and directly related to the risk of coronary occlusion >50%. In contrast, this result was not significant in genotypes of ANGPTL3 between non-ISR and ISR groups.

conclusionThe outcomes of this study showed that rs1748195 polymorphism at the ANGPTL3 gene loci is associated with an elevated risk for the existence of a coronary occlusion of >50%.

Indexed as

Coronary Artery DiseaseCoronary OcclusionCoronary RestenosisAngiographyAngiopoietin-Like Protein 3HumansIranPolymorphism, GeneticAngiopoietin-Like Protein 3ANGPTL3 protein, humanangiographyangiopoietin-like3 (ANGPTL3)atherosclerosiscardiovascular diseases (CVD)

Identifiers

PMID36416040
PMCPMC10009914
OpenAlexW4309721252

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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.