Evidence map›Paper›PMID 34091593›Full record

ArticleInternational journal of obesity (2005)2021

Oxytocin receptor gene polymorphism and low serum oxytocin level are associated with hyperphagia and obesity in adolescents.

Gönül Çatli, Sezer Acar, Gülten Cingöz, Khayala Rasulova, Ayça Kanat Yarim, Hamide Uzun, Tuncay Küme, Sefa Kızıldağ, Bumin Nuri Dündar, Ayhan Abacı

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In one paragraph

Article in International journal of obesity (2005), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 10% 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, 1 synthesis or guideline pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Roles of the Oxytocin Receptor (OXTR) in Human Diseases.International journal of molecular sciences · 2023
    Review
  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

10 authors at 3 institutions in 1 country.

Gönül ÇatliDepartment of Pediatric Endocrinology, Izmir KatipÇelebi University, Faculty of Medicine, İzmir, Turkey. gonulcatli@gmail.com.ORCID http://orcid.org/0000-0002-0488-6377
Sezer AcarDepartment of Pediatric Endocrinology, Dokuz Eylül University, Faculty of Medicine, İzmir, Turkey.
Gülten CingözDepartment of Pediatrics, Sağlik Bilimleri University, Tepecik Training and Research Hospital, İzmir, Turkey.ORCID http://orcid.org/0000-0002-3002-480X
Khayala RasulovaDepartment of Medical Biology and Genetics, Dokuz Eylül University, Faculty of Medicine, İzmir, Turkey.
Ayça Kanat YarimDepartment of Medical Biology and Genetics, Dokuz Eylül University, Faculty of Medicine, İzmir, Turkey.
Hamide UzunDepartment of Nutrition and Dietetics, Sağlik Bilimleri University, Tepecik Training and Research Hospital, İzmir, Turkey.
Tuncay KümeDepartment of Biochemistry, Dokuz Eylül University, Faculty of Medicine, İzmir, Turkey.
Sefa KızıldağDepartment of Medical Biology and Genetics, Dokuz Eylül University, Faculty of Medicine, İzmir, Turkey.
Bumin Nuri DündarDepartment of Pediatric Endocrinology, Izmir KatipÇelebi University, Faculty of Medicine, İzmir, Turkey.
Ayhan AbacıDepartment of Pediatric Endocrinology, Dokuz Eylül University, Faculty of Medicine, İzmir, Turkey.
Dokuz Eylül University · TRIzmir Kâtip Çelebi University · TRSağlık Bilimleri Üniversitesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesIn recent years, oxytocin (OXT) and polymorphisms in the oxytocin receptor (OXTR) gene have been reported to play roles in obesity pathogenesis. However, there was no study evaluating OXTR gene variants in childhood obesity. The aim of the study was to investigate the relation of OXTR gene polymorphisms and serum OXT levels with metabolic and anthropometric parameters in obese and healthy adolescents. SUBJECTS/

methodsThe study was a multi-centered case-control study, which was conducted on obese and healthy adolescents aged between 12 and 17 years. Serum OXT and leptin levels were measured, and OXTR gene variants were studied by qPCR (rs53576) and RFLP (rs2254298) methods.

resultsA total of 250 obese and 250 healthy adolescents were included in this study. In the obese group, serum OXT level was lower and leptin level was higher than the control group. In the obese group, frequencies of homozygous mutant (G/G) and heterozygous (A/G) genotypes for rs53576 polymorphism were higher than the control group. Homozygous mutant(G/G) and heterozygous (A/G) genotypes for rs53576 polymorphism were found to increase the risk of obesity compared to the wild type (A/A) genotype [OR = 6.05 and OR = 3.06; p < 0.001, respectively]. In patients with homozygous mutant (G/G) and heterozygous (A/G) genotype for rs53576 polymorphism, serum OXT levels were lower than the wild type (A/A) genotype. In the obese group, hyperphagia score was higher than the control group and correlated negatively with serum OXT level.

conclusionsThis study revealed that low serum OXT level, which is associated with hyperphagia may be an underlying cause for obesity in adolescents. For rs53576 polymorphism of the OXTR gene, obesity risk is higher in patients with homozygous mutant(G/G) and heterozygous(A/G)genotypes.

Indexed as

Polymorphism, GeneticAdolescentCase-Control StudiesFemaleHumansHyperphagiaMaleOxytocinPediatric ObesityReceptors, OxytocinOXTR protein, humanOxytocinReceptors, Oxytocin

Identifiers

PMID34091593
OpenAlexW3170625568

What OpenQuestion holds

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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.