Evidence map›Paper›PMID 36518119›Full record

ArticleBioinformation2022

Gene polymorphism among hypertensive patients with coronary artery disease.

D Selvakumar, C K Vijayasamundeeswari, E Gnanadesigan, N Sivasubramanian

Open access · hybridAbstract read
In one paragraph

Article in Bioinformation, 2022. 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
0.3field-weighted citation impact, top 41% 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, 2 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

4 authors at 1 institution in 1 country.

D SelvakumarDepartment of Biochemistry, Vinayaka Mission's Kirupananda Variyar Medical college and Hospitals, Salem, Vinayaka Mission's Research Foundation (Deemed to be University), Salem -636 308, Tamilnadu, India.
C K VijayasamundeeswariDepartment of Biochemistry, Vinayaka Mission's Kirupananda Variyar Medical college and Hospitals, Salem, Vinayaka Mission's Research Foundation (Deemed to be University), Salem -636 308, Tamilnadu, India.
E GnanadesiganDepartment of Physiology, Nootan Medical College & Research Centre, Sankalchand Patel University, Visnagar - 384315, Gujarat, India.
N SivasubramanianDepartment of Psychiatric Nursing, Nootan College of Nursing, Sankalchand Patel University, Visnagar- 384315, Gujarat, India.
Motilal Nehru Medical College · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The obstruction of the coronary arteries causes Coronary Artery Disease (CAD). It has been reported that interleukin-6 gene is related to the development of cardiovascular diseases such as atherosclerosis and coronary artery disease. This was due to the large variability and short half-life of interleukin 6 (IL-6). There are few studies on the link between interleukin 6 and CAD on the patients with hypertension. Therefore, goal of this study was to see if there is a link between IL-6 gene polymorphisms and coronary artery disease with hypertension patients. The polymorphisms were carried out by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP). The data was determined for statistical significance using chi-square analysis. A significant difference was found in the GG genotype of IL-6 -174, which was more frequent in cases of CAD (48.67 %) than in controls (8%) and 95% CI was 0.473455 - 0.500326; P<0.010620511. The GG genotype of IL-6-572C/G polymorphism was more frequent in cases of CAD (42.6%) compared with controls (8%) and 95% CI 0.386724 - 0.480945; P<0.017939631). likewise, significant association of variant allele G with CAD patients was reported. Hypertension was significantly higher among patients as compared to controls (P<0.022847535). Our findings indicated that both gene polymorphisms may be associated with development of CAD.

Indexed as

CADgene polymorphismhypertensionIL-6 -174IL-6-572

Identifiers

PMID36518119
PMCPMC9722429
OpenAlexW4292559662

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.