Evidence map›Paper›PMID 26597055›Full record

ArticleIranian biomedical journal2016

Association Study of rs1333040 and rs1004638 Polymorphisms in the 9p21 Locus with Coronary Artery Disease in Southwest of Iran.

Khadijeh Golabgir Khademi, Ali Mohammad Foroughmand, Hamid Galehdari, Saied Yazdankhah, Mahdi Pourmahdi Borujeni, Zahra Shahbazi, Parvaneh Dinarvand

Open access · greenAbstract read
In one paragraph

Article in Iranian biomedical journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-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, 9 citations in OpenAlex.

  1. Prognostic value ofInternational journal of cardiology. Cardiovascular risk and prevention · 2025
    Article
  2. Article
  3. Review
  4. Article
  5. 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

7 authors at 2 institutions in 1 country.

Khadijeh Golabgir KhademiDept. of Genetics, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Ali Mohammad ForoughmandDept. of Genetics, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Hamid GalehdariDept. of Genetics, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Saied YazdankhahDept. of Medicine, Jondi Shapour University of Medical Science, Ahvaz, Iran.
Mahdi Pourmahdi BorujeniDept. of Food Hygiene, Faculty of Veterinary medicine, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Zahra ShahbaziDept. of Genetics, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Parvaneh DinarvandDept. of Genetics, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Shahid Chamran University of Ahvaz · IRAhvaz Jundishapur University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronary artery disease (CAD) is a multifactorial and heterogenic disease. Recently, genome-wide association studies have reported that rs1333040 (C/T) and rs1004638 (A/T) single nucleotide polymorphisms (SNPs) in the 9p21 locus have very strong association with CAD. This study aimed to examine these associations in Southwest of Iran.

methodsBlood samples were collected from 200 CAD patients and 110 healthy individuals with no CAD. The association of two SNPs with CAD was evaluated by PCR and restriction fragment length polymorphism.

resultsChi-square test showed no association between rs1333040 SNP and CAD (X2: 4.66, df: 2, P=0.09). Also, there was no association between rs1004638 SNP and CAD (X2: 0.27, df: 2, P=0.88).

conclusionNo association was observed between rs1333040 and rs1004638 SNPs in the 9P21 region and CAD in Southwest of Iran.

Indexed as

AgedCoronary Artery DiseaseFemaleGenetic LociGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansIranMaleMiddle AgedPolymorphism, Single NucleotideRisk FactorsRNA, Long NoncodingCDKN2B antisense RNA, humanRNA, Long NoncodingCoronary artery diseaseGenetic association studyIranSingle nucleotide polymorphisms

Identifiers

PMID26597055
PMCPMC4726893
OpenAlexW2342172915

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.