Evidence map›Paper›PMID 27611604›Full record

ArticleJournal of clinical research in pediatric endocrinology2016

Effect of Cytokine Signaling 3 Gene Polymorphisms in Childhood Obesity.

Mehmet Boyraz, Ediz Yeşilkaya, Fatih Ezgü, Aysun Bideci, Haldun Doğan, Korkut Ulucan, Peyami Cinaz

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical research in pediatric endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 30% 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Innate-Immunity Genes in Obesity.Journal of personalized medicine · 2021
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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

7 authors at 3 institutions in 1 country.

Mehmet Boyraz
Ediz Yeşilkaya
Fatih Ezgü
Aysun Bideci
Haldun Doğan
Korkut UlucanMarmara University Faculty of Dentistry, Department of Medical Biology and Genetics, İstanbul, Turkey, Phone: +90 216 400 22 22- 2409 E-mail: korkutulucan@hotmail.com.
Peyami Cinaz
Gazi University · TRIntergen (Turkey) · TRÜsküdar University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAlthough polymorphisms in suppressor of cytokine signaling 3 (SOCS3) was reported to be related to obesity, Metabolic syndrome (MS), and type 2 diabetes mellitus in various adult studies, there is a lack of data in children. In this study, we examined eight reported polymorphisms of SOCS3 in obese Turkish children and adolescent with and without MS and compared the results with that of controls.

methodsOne hundred and forty eight obese and 63 age- and sex-matched control subjects were enrolled in the study. Obesity classification was carried out according to body mass index. World Health Organization and National Cholesterol Education Program criteria were used for the diagnosis of MS. Genotyping procedure was carried out by polymerase chain reaction and Sanger sequencing protocol.

resultsThe frequency of rs2280148 polymorphism was significantly higher in obese subjects with MS than in the control group, whereas the frequency of rs8064821 polymorphism was significantly higher in obese subjects with MS than in obese children without MS.

conclusionThe significant associations of certain SOCS3 polymorphisms with obesity parameters in both MS and MS -related insulin resistance, hypertension, and fatty liver suggest that polymorphisms in this gene may play a role in the pathogenesis of MS and also that they can be potentially used as a marker for attenuated or aggressive disease.

Indexed as

Polymorphism, Single NucleotideAdolescentAllelesBlood GlucoseBody Mass IndexChildDiabetes Mellitus, Type 2FemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHumansInsulinLipidsLogistic ModelsMaleBlood GlucoseInsulinLipidsSOCS3 protein, humanSuppressor of Cytokine Signaling 3 Protein

Identifiers

PMID27611604
PMCPMC5198005
OpenAlexW2510212228

What OpenQuestion holds

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LicenceCC BY
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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.