Evidence map›Paper›PMID 36856592›Full record

ArticleAnatolian journal of cardiology2023

Fibrinogen-Aα THR312ALA Polymorphism is Associated to Chronic Thromboembolic Pulmonary Hypertension in Turkey.

Mustafa Çörtük, Bedrettin Yıldızeli, Ercan Kurar, Seyit Ali Kayış, Elif Tanrıverdi, Erdoğan Çetinkaya

Open access · diamondAbstract read
In one paragraph

Article in Anatolian journal of cardiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Association of Fibrinogen Aα Thr312Ala (rs6050) Polymorphism with Venous Thrombosis and Chronic Thromboembolic Pulmonary Hypertension: A Meta-Analysis.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    Pooled it
  2. 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

6 authors at 1 institution in 1 country.

Mustafa ÇörtükDepartment of Pulmonology, University of Health Sciences Yedikule Pulmonary Diseases and Thoracic Surgery Training and Research Hospital, İstanbul, Türkiye.
Bedrettin YıldızeliDepartment of Thoracic Surgery, Faculty of Medicine, Marmara University, İstanbul, Türkiye.
Ercan KurarDepartment of Medical Biology, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, Türkiye.
Seyit Ali KayışDepartment of Biostatistics, Faculty of Medicine, Bolu Abant İzzet Baysal University, Bolu, Türkiye.
Elif TanrıverdiDepartment of Pulmonology, University of Health Sciences Yedikule Pulmonary Diseases and Thoracic Surgery Training and Research Hospital, İstanbul, Türkiye.
Erdoğan ÇetinkayaDepartment of Pulmonology, University of Health Sciences Yedikule Pulmonary Diseases and Thoracic Surgery Training and Research Hospital, İstanbul, Türkiye.
Necmettin Erbakan University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundChronic thromboembolic pulmonary hypertension is a condition that occurs after mechanical obstruction of the pulmonary arteries by thrombus. Since the frequency and demographics of chronic thromboembolic pulmonary hypertension differ between countries, it is thought that genetic factors may play a role in its development. The aim of this study is to reveal the status of VKORC1, CYP2C9*3, CYP2C9*7, and fibrinogen-Aα THR312ALA gene polymorphisms in chronic thromboembolic pulmonary hypertension patients in Turkey.

methodsIn this prospective cross-sectional study, a total of 46 chronic thromboembolic pulmonary hypertension patients and 106 healthy volunteers were included. Polymerase chain reaction-restriction fragment length polymorphism method was used to determine candidate gene polymorphisms for chronic thromboembolic pulmonary hypertension. The general population parameters of each locus were calculated, and the relationship between dominant, codominant, and recessive genotype models and chronic thromboembolic pulmonary hypertension was analyzed.

resultsFor the fibrinogen-Aα gene, those with the THR/THR genotype were found to have a 13.51 (95% CI: 2.688-33.333) times less susceptibility rate to the disease than those with the ALA/THR genotype, the susceptibility of THR/ALA genotype to the disease was 5.026 (95% CI: 1.774-14.242) times more than those with ALA/ALA genotype. There was no difference between patient groups for VKORC1, CYP2C9*3 genes (P >.05). Since the CYP2C9*7 patient group was monomorphic for the ILE allele, the patient/control odds ratio and 95% CI could not be calculated.

conclusionThis study shows that there is an association between the fibrinogen-Aα gene ALA polymorphism at the amino acid position of 312 and the development of chronic thromboembolic pulmonary hypertension, but not between the CYP2C9 and VKORC1 gene polymorphisms.

Indexed as

FibrinogenHypertension, PulmonaryCross-Sectional StudiesCytochrome P-450 CYP2C9HumansPolymorphism, GeneticProspective StudiesTurkeyVitamin K Epoxide ReductasesCytochrome P-450 CYP2C9FibrinogenVitamin K Epoxide ReductasesVKORC1 protein, human

Identifiers

PMID36856592
PMCPMC9995549
OpenAlexW4322719391

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LicenceCC BY-NC
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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.