Evidence map›Paper›PMID 23065219›Full record

ArticleMolecular biology reports2013

DD genotype of ACE gene I/D polymorphism is associated with Behcet disease in a Turkish population.

Serbülent Yigit, Sengül Tural, Aydin Rüstemoglu, Ahmet Inanir, Ulker Gul, Goknur Kalkan, Songul Akkanet, Nevin Karakuş, Omer Ateş

Abstract read
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In one paragraph

Article in Molecular biology reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
  2. Association of polymorphisms ofJournal of genetics · 2024
    Article
  3. Review
  4. Article
  5. Human Ace D/I Polymorphism Could Affect the Clinicobiological Course of COVID-19.Journal of the renin-angiotensin-aldosterone system : JRAAS · 2021
    Article
  6. Article
  7. Article
  8. 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

9 authors at 3 institutions in 1 country.

Serbülent YigitDepartment of Medical Biology, Faculty of Medicine, Gaziosmapaşa University, Tokat, Turkey. serbulent.yigit@gmail.com
Sengül Tural
Aydin Rüstemoglu
Ahmet Inanir
Ulker Gul
Goknur Kalkan
Songul Akkanet
Nevin Karakuş
Omer Ateş
Tokat Gaziosmanpaşa Üniversitesi · TROndokuz Mayıs University · TRAnkara Numune Eğitim ve Araştırma Hastanesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Behcet's disease (BD) is a chronic, multi-systemic and inflammatory disorder. The local renin-angiotensin system (RAS) in the vessel wall plays a role in the endothelial control and contributes to inflammatory processes. Angiotensin-converting enzyme (ACE) is the regulatory component of the RAS. This study was conducted in Turkish patients with BD to determine the frequency of I/D polymorphism genotypes of ACE gene. Genomic DNA obtained from 566 persons (266 patients with BD and 300 healthy controls). ACE gene I/D polymorphism genotypes were determined using polymerase chain reaction using I and D allele-specific primers. There was statistically significant difference between the groups with respect to genotype distribution (p < 0.001). This study is the largest study in Turkish population that ACE gene I/D polymorphism investigated in BD. As a result of this study, ACE gene I/D polymorphism DD genotype could be a genetic marker in BD in Turkish study population.

Indexed as

Genetic Predisposition to DiseaseGenotypePolymorphism, GeneticAdolescentAdultAgedAged, 80 and overBehcet SyndromeCase-Control StudiesFemaleHumansMaleMiddle AgedPeptidyl-Dipeptidase ATurkeyYoung AdultACE protein, humanPeptidyl-Dipeptidase A

Identifiers

PMID23065219
OpenAlexW1985223884

What OpenQuestion holds

Textmetadata
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.