Evidence map›Paper›PMID 23480670›Full record

ArticleJournal of cellular and molecular medicine2013

Frequency of angiotensin II type 1 receptor gene polymorphism in Turkish acute stroke patients.

Kurt Hulyam, Bayramoglu Aysegul, Gunes Hasan Veysi, Ozbabalik Demet, Degirmenci Irfan, Colak Ertugrul, Cosan Turgut Didem, Bayram Banu, Dikmen Miris

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Genetic Variants Associated with High Susceptibility of Premature Ischemic Stroke.Journal of the renin-angiotensin-aldosterone system : JRAAS · 2023
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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

9 authors at 4 institutions in 1 country.

Kurt HulyamDepartment of Medical Biology, Faculty of Medicine, Eskisehir Osmangazi University, Eskisehir 26480, Turkey. hkurtayda@gmail.com
Bayramoglu Aysegul
Gunes Hasan Veysi
Ozbabalik Demet
Degirmenci Irfan
Colak Ertugrul
Cosan Turgut Didem
Bayram Banu
Dikmen Miris
Eskişehir Osmangazi University · TRAnadolu University · TRArtvin Coruh University · TRMuğla University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study was performed in acute stroke patients in the Turkish population to determine the frequency of the A1166C polymorphism in the AT1 gene and to examine the role of this polymorphism in acute stroke development. In this study, 257 genomic DNA samples were analysed (from 206 acute stroke patients and 51 healthy individuals). Genomic DNA was prepared from peripheral blood using the salt-extraction method. The presence of the A1166C polymorphism in the AT1 gene was determined using the polymerase chain reaction (PCR)-restriction fragment length polymorphism (RFLP) method. PCR products were separated by 2% agarose gel electrophoresis and visualized by a charge-coupled device (CCD) camera. In this study, the allele frequency at the A1166C position was 92% A and 8% C for control and 97% A and 3% C for patients. This difference in allele frequency between the control group and the patient group was not statistically significant. However, genotype and allele frequencies showed a significant difference (P < 0.001) in the control and the patient groups. The results of this study show no relationship between the A1166C polymorphism in the AT1 gene and acute stroke in the Turkish population.

Indexed as

Polymorphism, Single NucleotideAgedCase-Control StudiesFemaleGene FrequencyGenetic Association StudiesGenotypeHumansMaleMiddle AgedPolymorphism, Restriction Fragment LengthReceptor, Angiotensin, Type 1Sequence Analysis, DNAStrokeTurkeyReceptor, Angiotensin, Type 1

Identifiers

PMID23480670
PMCPMC3822648
OpenAlexW1981907951

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.