Evidence map›Paper›PMID 35673309›Full record

ArticleCureus2022

Evaluation of the Association of Single Nucleotide Polymorphism rs2229238 in Interleukin 6 Receptor Alpha (IL6RA) Gene With the Risk of Preeclampsia.

Nagarjuna Sivaraj, Vijaya Rachel K, Tarun Kumar Suvvari, Shilaja Prasad, Boppana Sri Harsha, Vineetha Majji, Pradeep Kumar Vegi, Papa Kusuma Bunga

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Article in Cureus, 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
–field-weighted citation impact
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.

  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

8 authors.

Nagarjuna SivarajResearch and Development, Great Eastern Medical School and Hospital, Srikakulam, IND.
Vijaya Rachel KBiochemistry and Bioinformatics, Gandhi Institute of Technology and Management (Deemed To Be University), Visakhapatnam, IND.
Tarun Kumar SuvvariMedicine and Surgery, Dr. Nandamuri Taraka Rama Rao (NTR) University of Health Sciences, Vijayawada, IND.
Shilaja PrasadObstetrics and Gynaecology, Great Eastern Medical School and Hospital, Srikakulam, IND.
Boppana Sri HarshaGeneral Medicine, Great Eastern Medical School and Hospital, Srikakulam, IND.
Vineetha MajjiCentral Research Laboratory, Great Eastern Medical School and Hospital, Srikakulam, IND.
Pradeep Kumar VegiBiochemistry, Great Eastern Medical School and Hospital, Srikakulam, IND.
Papa Kusuma BungaResearch and Development, Great Eastern Medical School and Hospital, Srikakulam, IND.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction Many studies have gone into single nucleotide polymorphisms (SNPs) in inflammatory-associated genes and preeclampsia risk; still, the findings are inconclusive. The current study aims to evaluate the association of SNP rs2229238 in the interleukin 6 receptor alpha (IL6RA) gene with the risk of preeclampsia. Methodology An observational case-control study was conducted and 216 patients were included in this study. Of the patients, 104 were normotensive subjects and 112 were subjects with preeclampsia. Genotyping for SNP rs2229238 was performed by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method. Results The genotype allocation of the SNP 2229238 C/A polymorphism was not different in preeclampsia subjects (CC: 42%; CA: 42%; AA: 16%) and normotensive pregnant women (CC: 37%; CA: 48%; AA: 15%) (p-value = 0.73). The frequency of the A allele was 34% in preeclampsia subjects and 31% in normotensive pregnancies. There was no significant variation seen in the allele frequencies among cases and the control population. Conclusion Our study reported that there is no significant relation between preeclampsia and IL6RA SNP rs2229238. Also, there is no significance in the allele frequencies among both cases and control groups.

Indexed as

geneil6rainflammationinterleukinspreeclampsiasingle nucleotide polymorphism

Identifiers

PMID35673309
PMCPMC9165912

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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.