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

Background/Objectives In 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...

Full description

Saved in:
Bibliographic Details
Published inInternational Journal of Obesity Vol. 45; no. 9; pp. 2064 - 2073
Main Authors Çatli, Gönül, Acar, Sezer, Cingöz, Gülten, Rasulova, Khayala, Yarim, Ayça Kanat, Uzun, Hamide, Küme, Tuncay, Kızıldağ, Sefa, Dündar, Bumin Nuri, Abacı, Ayhan
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.09.2021
Nature Publishing Group
Subjects
Online AccessGet full text

Cover

Loading…
Abstract Background/Objectives In 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/Methods The 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. Results A 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. Conclusions This 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.
AbstractList In 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.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.The 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.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.A 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.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.This 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.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.
In 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. A 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. This 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.
In 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. The 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. A 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. This 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.
Background/Objectives In 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/Methods The 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. Results A 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. Conclusions This 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.
Background/Objectives In 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/Methods The 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. Results A 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. Conclusions This 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.
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.
Audience Academic
Author Yarim, Ayça Kanat
Acar, Sezer
Rasulova, Khayala
Abacı, Ayhan
Cingöz, Gülten
Uzun, Hamide
Çatli, Gönül
Küme, Tuncay
Dündar, Bumin Nuri
Kızıldağ, Sefa
Author_xml – sequence: 1
  givenname: Gönül
  orcidid: 0000-0002-0488-6377
  surname: Çatli
  fullname: Çatli, Gönül
  email: gonulcatli@gmail.com
  organization: Department of Pediatric Endocrinology, Izmir KatipÇelebi University, Faculty of Medicine
– sequence: 2
  givenname: Sezer
  surname: Acar
  fullname: Acar, Sezer
  organization: Department of Pediatric Endocrinology, Dokuz Eylül University, Faculty of Medicine
– sequence: 3
  givenname: Gülten
  orcidid: 0000-0002-3002-480X
  surname: Cingöz
  fullname: Cingöz, Gülten
  organization: Department of Pediatrics, Sağlik Bilimleri University, Tepecik Training and Research Hospital
– sequence: 4
  givenname: Khayala
  surname: Rasulova
  fullname: Rasulova, Khayala
  organization: Department of Medical Biology and Genetics, Dokuz Eylül University, Faculty of Medicine
– sequence: 5
  givenname: Ayça Kanat
  surname: Yarim
  fullname: Yarim, Ayça Kanat
  organization: Department of Medical Biology and Genetics, Dokuz Eylül University, Faculty of Medicine
– sequence: 6
  givenname: Hamide
  surname: Uzun
  fullname: Uzun, Hamide
  organization: Department of Nutrition and Dietetics, Sağlik Bilimleri University, Tepecik Training and Research Hospital
– sequence: 7
  givenname: Tuncay
  surname: Küme
  fullname: Küme, Tuncay
  organization: Department of Biochemistry, Dokuz Eylül University, Faculty of Medicine
– sequence: 8
  givenname: Sefa
  surname: Kızıldağ
  fullname: Kızıldağ, Sefa
  organization: Department of Medical Biology and Genetics, Dokuz Eylül University, Faculty of Medicine
– sequence: 9
  givenname: Bumin Nuri
  surname: Dündar
  fullname: Dündar, Bumin Nuri
  organization: Department of Pediatric Endocrinology, Izmir KatipÇelebi University, Faculty of Medicine
– sequence: 10
  givenname: Ayhan
  surname: Abacı
  fullname: Abacı, Ayhan
  organization: Department of Pediatric Endocrinology, Dokuz Eylül University, Faculty of Medicine
BackLink https://www.ncbi.nlm.nih.gov/pubmed/34091593$$D View this record in MEDLINE/PubMed
BookMark eNp9ks9rFTEQgINU7Gv1H_AgAUF62Zpskv1xLEWrUOhFzyEvO3kvJZusSdb68J8329daW6TkkDB8X2aYmSN04IMHhN5SckoJ6z4mTlnTVKSmFSFd21TiBVpRvjx43x6gFWGkrYhoxCE6SumaECIEqV-hQ8ZJT0XPVuj31a9dDtp6HEHDlEPEG_CAp-B2Y4jT1qYRKz9gF25wgjiPONwbDn6CwyoCVimViMow4Bubt3i7m6C4amPVrRzWkGze4SKpIThIGnxOr9FLo1yCN3f3Mfr--dO38y_V5dXF1_Ozy0rzluVq0EBpq_s1Ba4Fo6IzhLG2NkAbXXdG9a2hqu5VawwA06yrDTOi40r066YW7Bid7P-dYvgxQ8pytKUC55SHMCdZkI5w3nJe0PdP0OswR1-qK1TDWFP61zxQG-VAWm9Cjkovn8qzpq27vmOkL9Tpf6hyBhitLqM0tsQfCR_-EbagXN6m4OZsg0-PwXd3Vc7rEQY5RTuquJP3Yy1AvQd0DClFMH8RSuSyO3K_O7LsjrzdHbm0qXsiaZvVkrzUbd3zKturqeTxG4gPbXvG-gM1u9et
CitedBy_id crossref_primary_10_1186_s43043_024_00212_7
crossref_primary_10_1016_j_bbrep_2024_101666
crossref_primary_10_3390_biomedicines11123109
crossref_primary_10_52727_2078_256X_2024_20_4_342_354
crossref_primary_10_3390_ijms24043887
crossref_primary_10_1111_ijpo_12871
crossref_primary_10_1186_s43042_025_00680_0
crossref_primary_10_7554_eLife_75718
Cites_doi 10.1210/endrev/bnz012
10.3389/fnins.2017.00221
10.1002/oby.22284
10.1038/oby.2007.216
10.3181/00379727-168-41245
10.1152/ajpregu.00008.2002
10.1016/S0022-3476(85)80501-1
10.18632/aging.100408
10.4274/jcrpe.3963
10.1152/ajpregu.00441.2014
10.1016/j.psyneuen.2010.07.003
10.3389/fendo.2014.00058
10.1002/oby.20646
10.1016/j.numecd.2005.12.007
10.1007/s00424-002-0925-7
10.1152/ajpendo.00296.2011
10.1210/jc.2019-00643
10.1210/jc.2014-2206
10.1016/j.bbr.2017.04.036
10.3389/fendo.2015.00119
10.1002/ajmg.a.37488
10.1530/JOE-13-0417
10.17795/gct-27904
10.1371/journal.pone.0061477
10.1001/jamapediatrics.2016.2332
10.1038/s41598-018-20963-4
10.1152/ajpregu.00344.2014
10.15761/JSIN.1000114
10.1152/ajpendo.00196.2011
10.1016/S0022-3476(05)80382-8
10.1016/S1096-6374(03)00077-7
10.1097/YPG.0000000000000096
10.1016/j.regpep.2006.03.008
10.1016/j.neulet.2007.02.001
10.1007/BF03350119
10.4274/jcrpe.galenos.2019.2019.0127
10.1038/nutd.2017.24
10.1111/j.1748-1716.1985.tb07708.x
10.1016/0031-9384(81)90366-8
10.4274/jcrpe.2183
10.1074/jbc.M112.365049
ContentType Journal Article
Copyright The Author(s), under exclusive licence to Springer Nature Limited 2021
2021. The Author(s), under exclusive licence to Springer Nature Limited.
COPYRIGHT 2021 Nature Publishing Group
The Author(s), under exclusive licence to Springer Nature Limited 2021.
Copyright_xml – notice: The Author(s), under exclusive licence to Springer Nature Limited 2021
– notice: 2021. The Author(s), under exclusive licence to Springer Nature Limited.
– notice: COPYRIGHT 2021 Nature Publishing Group
– notice: The Author(s), under exclusive licence to Springer Nature Limited 2021.
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7T2
7TK
7TS
7X2
7X7
7XB
88E
88G
8AO
8C1
8FE
8FH
8FI
8FJ
8FK
ABUWG
AEUYN
AFKRA
ATCPS
AZQEC
BBNVY
BENPR
BHPHI
C1K
CCPQU
DWQXO
FYUFA
GHDGH
GNUQQ
HCIFZ
K9.
LK8
M0K
M0S
M1P
M2M
M7P
PHGZM
PHGZT
PJZUB
PKEHL
PPXIY
PQEST
PQGLB
PQQKQ
PQUKI
PRINS
PSYQQ
Q9U
7X8
DOI 10.1038/s41366-021-00876-5
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Central (Corporate)
Health and Safety Science Abstracts (Full archive)
Neurosciences Abstracts
Physical Education Index
Agricultural Science Collection
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
Psychology Database (Alumni)
ProQuest Pharma Collection
Public Health Database
ProQuest SciTech Collection
ProQuest Natural Science Collection
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest One Sustainability
ProQuest Central UK/Ireland
Agricultural & Environmental Science Collection
ProQuest Central Essentials Local Electronic Collection Information
Biological Science Collection
ProQuest Central
Natural Science Collection
Environmental Sciences and Pollution Management
ProQuest One Community College
ProQuest Central Korea
Health Research Premium Collection
Health Research Premium Collection (Alumni)
ProQuest Central Student
SciTech Premium Collection
ProQuest Health & Medical Complete (Alumni)
ProQuest Biological Science Collection
Agriculture Science Database
Health & Medical Collection (Alumni Edition)
PML(ProQuest Medical Library)
Psychology Database
Biological Science Database
ProQuest Central Premium
ProQuest One Academic
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Applied & Life Sciences
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
ProQuest One Psychology
ProQuest Central Basic
MEDLINE - Academic
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Agricultural Science Database
ProQuest One Psychology
ProQuest Central Student
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
SciTech Premium Collection
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Natural Science Collection
ProQuest Pharma Collection
ProQuest Central China
Physical Education Index
Environmental Sciences and Pollution Management
ProQuest Central
ProQuest One Applied & Life Sciences
ProQuest One Sustainability
ProQuest Health & Medical Research Collection
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
Natural Science Collection
ProQuest Central Korea
Health & Medical Research Collection
Agricultural & Environmental Science Collection
Biological Science Collection
Health & Safety Science Abstracts
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest Public Health
ProQuest Biological Science Collection
ProQuest Central Basic
ProQuest One Academic Eastern Edition
Agricultural Science Collection
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Psychology Journals (Alumni)
Biological Science Database
ProQuest SciTech Collection
Neurosciences Abstracts
ProQuest Hospital Collection (Alumni)
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest Psychology Journals
ProQuest One Academic UKI Edition
ProQuest One Academic
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic

MEDLINE



Agricultural Science Database
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 3
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
Public Health
Diet & Clinical Nutrition
Recreation & Sports
EISSN 1476-5497
EndPage 2073
ExternalDocumentID A672898309
34091593
10_1038_s41366_021_00876_5
Genre Research Support, Non-U.S. Gov't
Journal Article
GeographicLocations Turkey
GeographicLocations_xml – name: Turkey
GroupedDBID .55
.GJ
29J
36B
39C
5RE
7X2
7X7
8R4
8R5
A8Z
ABDBF
ABOCM
ABUWG
ACUHS
ADBBV
AFFNX
AI.
ALMA_UNASSIGNED_HOLDINGS
ATCPS
AZQEC
B0M
BAWUL
BENPR
BHPHI
BPHCQ
DIK
DWQXO
EAD
EAP
EBC
EBD
EBS
EMB
EMK
EMOBN
EPL
ESX
F5P
FYUFA
GNUQQ
HCIFZ
IAO
IHR
ITC
J5H
M0K
M1P
M2M
MVM
NAO
OK1
Q2X
RNT
RNTTT
SV3
TUS
VH1
WH7
X7M
ZGI
ZXP
~8M
AAYXX
CITATION
---
-Q-
..I
.L3
.XZ
0R~
1CY
2FS
2WC
4.4
406
53G
5GY
70F
88E
8AO
8C1
8FE
8FH
8FI
8FJ
AACDK
AAHBH
AANZL
AASML
AATNV
AAWTL
AAYZH
ABAKF
ABAWZ
ABBRH
ABCQX
ABDBE
ABFSG
ABIVO
ABJNI
ABLJU
ABRTQ
ABZZP
ACAOD
ACGFS
ACKTT
ACPRK
ACRQY
ACSTC
ACZOJ
ADHUB
ADXHL
AEFQL
AEJRE
AEMSY
AENEX
AEUYN
AEVLU
AEXYK
AEZWR
AFBBN
AFDZB
AFHIU
AFKRA
AFRAH
AFSHS
AGAYW
AGHAI
AGQEE
AHMBA
AHSBF
AHWEU
AIGIU
AILAN
AIXLP
AJRNO
ALFFA
ALIPV
AMYLF
APEBS
ATHPR
AXYYD
AYFIA
BBNVY
BKKNO
BVXVI
CCPQU
CGR
CS3
CUY
CVF
DNIVK
DPUIP
DU5
E3Z
EBLON
ECM
EE.
EIF
EIOEI
EJD
FDQFY
FERAY
FIGPU
FIZPM
FSGXE
HMCUK
HZ~
IHW
INH
INR
IPY
IWAJR
JSO
JZLTJ
KQ8
L7B
M7P
NPM
NQJWS
O9-
OVD
P2P
P6G
PHGZM
PHGZT
PJZUB
PPXIY
PQGLB
PQQKQ
PROAC
PSQYO
PSYQQ
RNS
ROL
SNX
SNYQT
SOHCF
SOJ
SRMVM
SWTZT
TAOOD
TBHMF
TDRGL
TEORI
TR2
TSG
UKHRP
~KM
3V.
7T2
7TK
7TS
7XB
8FK
C1K
K9.
LK8
PKEHL
PQEST
PQUKI
PRINS
Q9U
7X8
ID FETCH-LOGICAL-c473t-dce117c9b1e4c53158f03372fe16c28fa97f1a29a7ffee3c382f3f584a59b6253
IEDL.DBID 7X7
ISSN 0307-0565
1476-5497
IngestDate Thu Jul 10 22:46:40 EDT 2025
Sat Aug 23 12:50:56 EDT 2025
Tue Jun 17 21:12:57 EDT 2025
Tue Jun 10 20:34:12 EDT 2025
Thu May 22 21:10:58 EDT 2025
Mon Jul 21 06:03:57 EDT 2025
Tue Jul 01 03:02:03 EDT 2025
Thu Apr 24 22:55:42 EDT 2025
Fri Feb 21 02:39:08 EST 2025
IsPeerReviewed true
IsScholarly true
Issue 9
Language English
License 2021. The Author(s), under exclusive licence to Springer Nature Limited.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c473t-dce117c9b1e4c53158f03372fe16c28fa97f1a29a7ffee3c382f3f584a59b6253
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0002-0488-6377
0000-0002-3002-480X
PMID 34091593
PQID 2563365026
PQPubID 38864
PageCount 10
ParticipantIDs proquest_miscellaneous_2538044744
proquest_journals_2563365026
gale_infotracmisc_A672898309
gale_infotracacademiconefile_A672898309
gale_healthsolutions_A672898309
pubmed_primary_34091593
crossref_primary_10_1038_s41366_021_00876_5
crossref_citationtrail_10_1038_s41366_021_00876_5
springer_journals_10_1038_s41366_021_00876_5
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2021-09-01
PublicationDateYYYYMMDD 2021-09-01
PublicationDate_xml – month: 09
  year: 2021
  text: 2021-09-01
  day: 01
PublicationDecade 2020
PublicationPlace London
PublicationPlace_xml – name: London
– name: England
PublicationTitle International Journal of Obesity
PublicationTitleAbbrev Int J Obes
PublicationTitleAlternate Int J Obes (Lond)
PublicationYear 2021
Publisher Nature Publishing Group UK
Nature Publishing Group
Publisher_xml – name: Nature Publishing Group UK
– name: Nature Publishing Group
References Neyzi, Bundak, Gokcay, Gunoz, Furman, Darendeliler (CR16) 2015; 7
Johnson, Manzardo, Miller, Driscoll, Butler (CR9) 2016; 170
Hoybye, Barkeling, Espelund, Petersson, Thoren (CR40) 2003; 13
Dykens, Maxwell, Pantino, Kossler, Roof (CR22) 2007; 15
Altszuler, Hampshire (CR37) 1981; 168
Jacob, Brune, Carter, Leventhal, Lord, Cook (CR8) 2007; 417
Gajdosechova, Krskova, Segarra, Spolcova, Suski, Olszanecki (CR32) 2014; 220
Roth, D’Ambrosio, Elfers (CR12) 2016; 2
Ohlsson, Truedsson, Djerf, Sundler (CR3) 2006; 135
Blevins, Graham, Morton, Bales, Schwartz, Baskin (CR28) 2015; 308
Morton, Thatcher, Reidelberger, Ogimoto, Wolden-Hanson, Baskin (CR7) 2012; 302
Qian, Zhu, Tang, Yu, Hu, Sun (CR33) 2014; 99
Colaianni, Sun, Di Benedetto, Tamma, Zhu, Cao (CR4) 2012; 287
Saravani, Tamendani, Narooie (CR1) 2015; 2
Yang, Dong, Guo, Han, Song, Gao (CR14) 2017; 11
Rosner, Prineas, Loggie, Daniels (CR19) 1993; 123
Altirriba, Poher, Rohner-Jeanrenaud (CR41) 2015; 6
Coiro, Passeri, Davoli, d’Amato, Gelmini, Fagnoni (CR34) 1988; 11
Zhang, Cai (CR26) 2011; 301
Maejima, Iwasaki, Yamahara, Kodaira, Sedbazar, Yada (CR25) 2011; 3
Rinaman, Rothe (CR30) 2002; 283
Bush, Allison, Miller, Deardorff, Adler, Boyce (CR42) 2017; 171
Mason, Katzmarzyk (CR18) 2018; 26
Melchers, Montag, Markett, Niazy, Gross-Bolting, Zimmermann (CR10) 2017; 329
Demir, Konakci, Ozkaya, Kasap Demir, Ozen, Aydin (CR17) 2019; 12
Iwasaki, Maejima, Suyama, Yoshida, Arai, Katsurada (CR27) 2015; 308
McCormack, Blevins, Lawson (CR2) 2020; 41
Sobrino Crespo, Perianes, Cachero, Puebla Jimenez, Barrios, Arilla Ferreiro (CR39) 2014; 5
Heymsfield, Avena, Baier, Brantley, Bray, Burnett (CR43) 2014; 22
Onodera, Ishitobi, Tanaka, Aizawa, Masuda, Inoue (CR11) 2015; 25
Stock, Uvnas-Moberg (CR38) 1985; 125
Tanner, Davies (CR20) 1985; 107
Binay, Paketci, Guzel, Samanci (CR24) 2017; 9
Weingarten, Scholz, Wohland, Horn, Stumvoll, Kovacs (CR36) 2019; 104
Spetter, Feld, Thienel, Preissl, Hege, Hallschmid (CR5) 2018; 8
CR23
Leibowitz, Hammer, Chang (CR6) 1981; 27
Stock, Granstrom, Backman, Matthiesen, Uvnas-Moberg (CR35) 1989; 13
Wu, Hung, Chang, Pau, Wang, Wang (CR29) 2002; 445
Thompson, Parker, Hallmayer, Waugh, Gotlib (CR13) 2011; 36
Valerio, Licenziati, Iannuzzi, Franzese, Siani, Riccardi (CR21) 2006; 16
Davis, Patte, Zai, Kennedy (CR15) 2017; 7
Zhang, Wu, Chen, Chen, Xu, Wu (CR31) 2013; 8
C Sobrino Crespo (876_CR39) 2014; 5
L Rinaman (876_CR30) 2002; 283
RJ Thompson (876_CR13) 2011; 36
S Yang (876_CR14) 2017; 11
H Zhang (876_CR31) 2013; 8
B Ohlsson (876_CR3) 2006; 135
JM Tanner (876_CR20) 1985; 107
C Mason (876_CR18) 2018; 26
SE McCormack (876_CR2) 2020; 41
Y Iwasaki (876_CR27) 2015; 308
MS Spetter (876_CR5) 2018; 8
G Colaianni (876_CR4) 2012; 287
MFJ Weingarten (876_CR36) 2019; 104
NR Bush (876_CR42) 2017; 171
REE Saravani (876_CR1) 2015; 2
Y Maejima (876_CR25) 2011; 3
CL Wu (876_CR29) 2002; 445
J Altirriba (876_CR41) 2015; 6
S Stock (876_CR38) 1985; 125
C Davis (876_CR15) 2017; 7
L Johnson (876_CR9) 2016; 170
O Neyzi (876_CR16) 2015; 7
G Valerio (876_CR21) 2006; 16
G Zhang (876_CR26) 2011; 301
V Coiro (876_CR34) 1988; 11
876_CR23
N Altszuler (876_CR37) 1981; 168
JE Blevins (876_CR28) 2015; 308
EM Dykens (876_CR22) 2007; 15
M Onodera (876_CR11) 2015; 25
B Rosner (876_CR19) 1993; 123
SB Heymsfield (876_CR43) 2014; 22
M Melchers (876_CR10) 2017; 329
CL Roth (876_CR12) 2016; 2
SF Leibowitz (876_CR6) 1981; 27
L Gajdosechova (876_CR32) 2014; 220
C Hoybye (876_CR40) 2003; 13
K Demir (876_CR17) 2019; 12
S Stock (876_CR35) 1989; 13
S Jacob (876_CR8) 2007; 417
C Binay (876_CR24) 2017; 9
GJ Morton (876_CR7) 2012; 302
W Qian (876_CR33) 2014; 99
References_xml – volume: 41
  start-page: 121
  year: 2020
  end-page: 45
  ident: CR2
  article-title: Metabolic effects of oxytocin
  publication-title: Endocr Rev
  doi: 10.1210/endrev/bnz012
– volume: 11
  start-page: 221
  year: 2017
  ident: CR14
  article-title: Serum oxytocin levels and an oxytocin receptor gene polymorphism (rs2254298) indicate social deficits in children and adolescents with autism spectrum disorders
  publication-title: Front Neurosci
  doi: 10.3389/fnins.2017.00221
– volume: 26
  start-page: 1815
  year: 2018
  ident: CR18
  article-title: Variability in waist circumference according to measurement site
  publication-title: Obesity
  doi: 10.1002/oby.22284
– volume: 15
  start-page: 1816
  year: 2007
  end-page: 26
  ident: CR22
  article-title: Assessment of hyperphagia in Prader-Willi syndrome
  publication-title: Obesity
  doi: 10.1038/oby.2007.216
– volume: 168
  start-page: 123
  year: 1981
  end-page: 4
  ident: CR37
  article-title: Intranasal instillation of oxytocin increases insulin and glucagon secretion
  publication-title: Proc Soc Exp Biol Med
  doi: 10.3181/00379727-168-41245
– volume: 283
  start-page: R99
  year: 2002
  end-page: 106
  ident: CR30
  article-title: GLP-1 receptor signaling contributes to anorexigenic effect of centrally administered oxytocin in rats
  publication-title: Am J Physiol Regul Integr Comp Physiol
  doi: 10.1152/ajpregu.00008.2002
– volume: 107
  start-page: 317
  year: 1985
  end-page: 29
  ident: CR20
  article-title: Clinical longitudinal standards for height and height velocity for North American children
  publication-title: J Pediatr
  doi: 10.1016/S0022-3476(85)80501-1
– volume: 3
  start-page: 1169
  year: 2011
  end-page: 77
  ident: CR25
  article-title: Peripheral oxytocin treatment ameliorates obesity by reducing food intake and visceral fat mass
  publication-title: Aging
  doi: 10.18632/aging.100408
– volume: 13
  start-page: 213
  year: 1989
  end-page: 22
  ident: CR35
  article-title: Elevated plasma levels of oxytocin in obese subjects before and after gastric banding
  publication-title: Int J Obes
– volume: 9
  start-page: 124
  year: 2017
  end-page: 31
  ident: CR24
  article-title: Irisin and oxytocin as predictors of metabolic parameters in obese children
  publication-title: J Clin Res Pediatr Endocrinol
  doi: 10.4274/jcrpe.3963
– volume: 308
  start-page: R431
  year: 2015
  end-page: 8
  ident: CR28
  article-title: Chronic oxytocin administration inhibits food intake, increases energy expenditure, and produces weight loss in fructose-fed obese rhesus monkeys
  publication-title: Am J Physiol Regul Integr Comp Physiol
  doi: 10.1152/ajpregu.00441.2014
– volume: 36
  start-page: 144
  year: 2011
  end-page: 7
  ident: CR13
  article-title: Oxytocin receptor gene polymorphism (rs2254298) interacts with familial risk for psychopathology to predict symptoms of depression and anxiety in adolescent girls
  publication-title: Psychoneuroendocrinology
  doi: 10.1016/j.psyneuen.2010.07.003
– volume: 5
  start-page: 58
  year: 2014
  ident: CR39
  article-title: Peptides and food intake
  publication-title: Front Endocrinol
  doi: 10.3389/fendo.2014.00058
– volume: 22
  start-page: S1
  year: 2014
  end-page: 17
  ident: CR43
  article-title: Hyperphagia: current concepts and future directions proceedings of the 2nd international conference on hyperphagia
  publication-title: Obesity
  doi: 10.1002/oby.20646
– volume: 16
  start-page: 279
  year: 2006
  end-page: 84
  ident: CR21
  article-title: Insulin resistance and impaired glucose tolerance in obese children and adolescents from Southern Italy
  publication-title: Nutr Metab Cardiovasc Dis
  doi: 10.1016/j.numecd.2005.12.007
– volume: 445
  start-page: 187
  year: 2002
  end-page: 93
  ident: CR29
  article-title: Involvement of cholecystokinin receptor in the inhibition of gastric emptying by oxytocin in male rats
  publication-title: Pflugers Arch
  doi: 10.1007/s00424-002-0925-7
– volume: 302
  start-page: E134
  year: 2012
  end-page: 44
  ident: CR7
  article-title: Peripheral oxytocin suppresses food intake and causes weight loss in diet-induced obese rats
  publication-title: Am J Physiol Endocrinol Metab
  doi: 10.1152/ajpendo.00296.2011
– volume: 104
  start-page: 5621
  year: 2019
  end-page: 32
  ident: CR36
  article-title: Circulating oxytocin is genetically determined and associated with obesity and impaired glucose tolerance
  publication-title: J Clin Endocrinol Metab
  doi: 10.1210/jc.2019-00643
– volume: 99
  start-page: 4683
  year: 2014
  end-page: 9
  ident: CR33
  article-title: Decreased circulating levels of oxytocin in obesity and newly diagnosed type 2 diabetic patients
  publication-title: J Clin Endocrinol Metab
  doi: 10.1210/jc.2014-2206
– volume: 329
  start-page: 35
  year: 2017
  end-page: 40
  ident: CR10
  article-title: The OXTR gene, implicit learning and social processing: Does empathy evolve from perceptual skills for details?
  publication-title: Behav Brain Res
  doi: 10.1016/j.bbr.2017.04.036
– volume: 6
  start-page: 119
  year: 2015
  ident: CR41
  article-title: Chronic oxytocin administration as a treatment against impaired leptin signaling or leptin resistance in obesity
  publication-title: Front Endocrinol
  doi: 10.3389/fendo.2015.00119
– ident: CR23
– volume: 170
  start-page: 594
  year: 2016
  end-page: 601
  ident: CR9
  article-title: Elevated plasma oxytocin levels in children with Prader-Willi syndrome compared with healthy unrelated siblings
  publication-title: Am J Med Genet A
  doi: 10.1002/ajmg.a.37488
– volume: 220
  start-page: 333
  year: 2014
  end-page: 43
  ident: CR32
  article-title: Hypooxytocinaemia in obese Zucker rats relates to oxytocin degradation in liver and adipose tissue
  publication-title: J Endocrinol
  doi: 10.1530/JOE-13-0417
– volume: 2
  start-page: 1
  year: 2015
  end-page: 5
  ident: CR1
  article-title: Oxytocin receptor gene polymorphisms in patients with diabetes
  publication-title: Gene Cell Tissue
  doi: 10.17795/gct-27904
– volume: 8
  start-page: e61477
  year: 2013
  ident: CR31
  article-title: Treatment of obesity and diabetes using oxytocin or analogs in patients and mouse models
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0061477
– volume: 171
  start-page: 61
  year: 2017
  end-page: 7
  ident: CR42
  article-title: Socioeconomic disparities in childhood obesity risk: association with an oxytocin receptor polymorphism
  publication-title: JAMA Pediatr
  doi: 10.1001/jamapediatrics.2016.2332
– volume: 8
  year: 2018
  ident: CR5
  article-title: Oxytocin curbs calorie intake via food-specific increases in the activity of brain areas that process reward and establish cognitive control
  publication-title: Sci Rep
  doi: 10.1038/s41598-018-20963-4
– volume: 308
  start-page: R360
  year: 2015
  end-page: 9
  ident: CR27
  article-title: Peripheral oxytocin activates vagal afferent neurons to suppress feeding in normal and leptin-resistant mice: a route for ameliorating hyperphagia and obesity
  publication-title: Am J Physiol Regul Integr Comp Physiol
  doi: 10.1152/ajpregu.00344.2014
– volume: 2
  start-page: 79
  year: 2016
  end-page: 84
  ident: CR12
  article-title: Activation of nuclear factor kappa B pathway and reduction of hypothalamic oxytocin following hypothalamic lesions
  publication-title: J Syst Integr Neurosci
  doi: 10.15761/JSIN.1000114
– volume: 301
  start-page: E1004
  year: 2011
  end-page: 12
  ident: CR26
  article-title: Circadian intervention of obesity development via resting-stage feeding manipulation or oxytocin treatment
  publication-title: Am J Physiol Endocrinol Metab
  doi: 10.1152/ajpendo.00196.2011
– volume: 123
  start-page: 871
  year: 1993
  end-page: 86
  ident: CR19
  article-title: Blood pressure nomograms for children and adolescents, by height, sex, and age, in the United States
  publication-title: J Pediatr
  doi: 10.1016/S0022-3476(05)80382-8
– volume: 13
  start-page: 322
  year: 2003
  end-page: 7
  ident: CR40
  article-title: Peptides associated with hyperphagia in adults with Prader-Willi syndrome before and during GH treatment
  publication-title: Growth Horm IGF Res
  doi: 10.1016/S1096-6374(03)00077-7
– volume: 25
  start-page: 212
  year: 2015
  ident: CR11
  article-title: Genetic association of the oxytocin receptor genes with panic, major depressive disorder, and social anxiety disorder
  publication-title: Psychiatr Genet
  doi: 10.1097/YPG.0000000000000096
– volume: 135
  start-page: 7
  year: 2006
  end-page: 11
  ident: CR3
  article-title: Oxytocin is expressed throughout the human gastrointestinal tract
  publication-title: Regul Pept
  doi: 10.1016/j.regpep.2006.03.008
– volume: 417
  start-page: 6
  year: 2007
  end-page: 9
  ident: CR8
  article-title: Association of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autism
  publication-title: Neurosci Lett
  doi: 10.1016/j.neulet.2007.02.001
– volume: 11
  start-page: 125
  year: 1988
  end-page: 8
  ident: CR34
  article-title: Oxytocin response to insulin-induced hypoglycemia in obese subjects before and after weight loss
  publication-title: J Endocrinol Investig
  doi: 10.1007/BF03350119
– volume: 12
  start-page: 125
  year: 2019
  end-page: 9
  ident: CR17
  article-title: New features for child metrics: further growth references and blood pressure calculations
  publication-title: J Clin Res Pediatr Endocrinol
  doi: 10.4274/jcrpe.galenos.2019.2019.0127
– volume: 7
  start-page: e279
  year: 2017
  ident: CR15
  article-title: Polymorphisms of the oxytocin receptor gene and overeating: the intermediary role of endophenotypic risk factors
  publication-title: Nutr Diabetes
  doi: 10.1038/nutd.2017.24
– volume: 125
  start-page: 205
  year: 1985
  end-page: 10
  ident: CR38
  article-title: Oxytocin infusions increase plasma levels of insulin and VIP but not of gastrin in conscious dogs
  publication-title: Acta Physiol Scand
  doi: 10.1111/j.1748-1716.1985.tb07708.x
– volume: 27
  start-page: 1031
  year: 1981
  end-page: 40
  ident: CR6
  article-title: Hypothalamic paraventricular nucleus lesions produce overeating and obesity in the rat
  publication-title: Physiol Behav
  doi: 10.1016/0031-9384(81)90366-8
– volume: 7
  start-page: 280
  year: 2015
  end-page: 93
  ident: CR16
  article-title: Reference values for weight, height, head circumference, and body mass index in Turkish children
  publication-title: J Clin Res Pediatr Endocrinol
  doi: 10.4274/jcrpe.2183
– volume: 287
  start-page: 29159
  year: 2012
  end-page: 67
  ident: CR4
  article-title: Bone marrow oxytocin mediates the anabolic action of estrogen on the skeleton
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M112.365049
– volume: 308
  start-page: R360
  year: 2015
  ident: 876_CR27
  publication-title: Am J Physiol Regul Integr Comp Physiol
  doi: 10.1152/ajpregu.00344.2014
– volume: 11
  start-page: 125
  year: 1988
  ident: 876_CR34
  publication-title: J Endocrinol Investig
  doi: 10.1007/BF03350119
– ident: 876_CR23
– volume: 308
  start-page: R431
  year: 2015
  ident: 876_CR28
  publication-title: Am J Physiol Regul Integr Comp Physiol
  doi: 10.1152/ajpregu.00441.2014
– volume: 5
  start-page: 58
  year: 2014
  ident: 876_CR39
  publication-title: Front Endocrinol
  doi: 10.3389/fendo.2014.00058
– volume: 99
  start-page: 4683
  year: 2014
  ident: 876_CR33
  publication-title: J Clin Endocrinol Metab
  doi: 10.1210/jc.2014-2206
– volume: 27
  start-page: 1031
  year: 1981
  ident: 876_CR6
  publication-title: Physiol Behav
  doi: 10.1016/0031-9384(81)90366-8
– volume: 107
  start-page: 317
  year: 1985
  ident: 876_CR20
  publication-title: J Pediatr
  doi: 10.1016/S0022-3476(85)80501-1
– volume: 3
  start-page: 1169
  year: 2011
  ident: 876_CR25
  publication-title: Aging
  doi: 10.18632/aging.100408
– volume: 16
  start-page: 279
  year: 2006
  ident: 876_CR21
  publication-title: Nutr Metab Cardiovasc Dis
  doi: 10.1016/j.numecd.2005.12.007
– volume: 104
  start-page: 5621
  year: 2019
  ident: 876_CR36
  publication-title: J Clin Endocrinol Metab
  doi: 10.1210/jc.2019-00643
– volume: 302
  start-page: E134
  year: 2012
  ident: 876_CR7
  publication-title: Am J Physiol Endocrinol Metab
  doi: 10.1152/ajpendo.00296.2011
– volume: 8
  year: 2018
  ident: 876_CR5
  publication-title: Sci Rep
  doi: 10.1038/s41598-018-20963-4
– volume: 329
  start-page: 35
  year: 2017
  ident: 876_CR10
  publication-title: Behav Brain Res
  doi: 10.1016/j.bbr.2017.04.036
– volume: 2
  start-page: 1
  year: 2015
  ident: 876_CR1
  publication-title: Gene Cell Tissue
  doi: 10.17795/gct-27904
– volume: 36
  start-page: 144
  year: 2011
  ident: 876_CR13
  publication-title: Psychoneuroendocrinology
  doi: 10.1016/j.psyneuen.2010.07.003
– volume: 123
  start-page: 871
  year: 1993
  ident: 876_CR19
  publication-title: J Pediatr
  doi: 10.1016/S0022-3476(05)80382-8
– volume: 170
  start-page: 594
  year: 2016
  ident: 876_CR9
  publication-title: Am J Med Genet A
  doi: 10.1002/ajmg.a.37488
– volume: 13
  start-page: 322
  year: 2003
  ident: 876_CR40
  publication-title: Growth Horm IGF Res
  doi: 10.1016/S1096-6374(03)00077-7
– volume: 6
  start-page: 119
  year: 2015
  ident: 876_CR41
  publication-title: Front Endocrinol
  doi: 10.3389/fendo.2015.00119
– volume: 168
  start-page: 123
  year: 1981
  ident: 876_CR37
  publication-title: Proc Soc Exp Biol Med
  doi: 10.3181/00379727-168-41245
– volume: 417
  start-page: 6
  year: 2007
  ident: 876_CR8
  publication-title: Neurosci Lett
  doi: 10.1016/j.neulet.2007.02.001
– volume: 220
  start-page: 333
  year: 2014
  ident: 876_CR32
  publication-title: J Endocrinol
  doi: 10.1530/JOE-13-0417
– volume: 11
  start-page: 221
  year: 2017
  ident: 876_CR14
  publication-title: Front Neurosci
  doi: 10.3389/fnins.2017.00221
– volume: 7
  start-page: 280
  year: 2015
  ident: 876_CR16
  publication-title: J Clin Res Pediatr Endocrinol
  doi: 10.4274/jcrpe.2183
– volume: 301
  start-page: E1004
  year: 2011
  ident: 876_CR26
  publication-title: Am J Physiol Endocrinol Metab
  doi: 10.1152/ajpendo.00196.2011
– volume: 125
  start-page: 205
  year: 1985
  ident: 876_CR38
  publication-title: Acta Physiol Scand
  doi: 10.1111/j.1748-1716.1985.tb07708.x
– volume: 283
  start-page: R99
  year: 2002
  ident: 876_CR30
  publication-title: Am J Physiol Regul Integr Comp Physiol
  doi: 10.1152/ajpregu.00008.2002
– volume: 135
  start-page: 7
  year: 2006
  ident: 876_CR3
  publication-title: Regul Pept
  doi: 10.1016/j.regpep.2006.03.008
– volume: 41
  start-page: 121
  year: 2020
  ident: 876_CR2
  publication-title: Endocr Rev
  doi: 10.1210/endrev/bnz012
– volume: 9
  start-page: 124
  year: 2017
  ident: 876_CR24
  publication-title: J Clin Res Pediatr Endocrinol
  doi: 10.4274/jcrpe.3963
– volume: 8
  start-page: e61477
  year: 2013
  ident: 876_CR31
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0061477
– volume: 22
  start-page: S1
  year: 2014
  ident: 876_CR43
  publication-title: Obesity
  doi: 10.1002/oby.20646
– volume: 25
  start-page: 212
  year: 2015
  ident: 876_CR11
  publication-title: Psychiatr Genet
  doi: 10.1097/YPG.0000000000000096
– volume: 171
  start-page: 61
  year: 2017
  ident: 876_CR42
  publication-title: JAMA Pediatr
  doi: 10.1001/jamapediatrics.2016.2332
– volume: 287
  start-page: 29159
  year: 2012
  ident: 876_CR4
  publication-title: J Biol Chem
  doi: 10.1074/jbc.M112.365049
– volume: 26
  start-page: 1815
  year: 2018
  ident: 876_CR18
  publication-title: Obesity
  doi: 10.1002/oby.22284
– volume: 2
  start-page: 79
  year: 2016
  ident: 876_CR12
  publication-title: J Syst Integr Neurosci
  doi: 10.15761/JSIN.1000114
– volume: 7
  start-page: e279
  year: 2017
  ident: 876_CR15
  publication-title: Nutr Diabetes
  doi: 10.1038/nutd.2017.24
– volume: 445
  start-page: 187
  year: 2002
  ident: 876_CR29
  publication-title: Pflugers Arch
  doi: 10.1007/s00424-002-0925-7
– volume: 12
  start-page: 125
  year: 2019
  ident: 876_CR17
  publication-title: J Clin Res Pediatr Endocrinol
  doi: 10.4274/jcrpe.galenos.2019.2019.0127
– volume: 15
  start-page: 1816
  year: 2007
  ident: 876_CR22
  publication-title: Obesity
  doi: 10.1038/oby.2007.216
– volume: 13
  start-page: 213
  year: 1989
  ident: 876_CR35
  publication-title: Int J Obes
SSID ssj0005502
ssj0033214
Score 2.4190178
Snippet Background/Objectives In recent years, oxytocin (OXT) and polymorphisms in the oxytocin receptor ( OXTR) gene have been reported to play roles in obesity...
In recent years, oxytocin (OXT) and polymorphisms in the oxytocin receptor (OXTR) gene have been reported to play roles in obesity pathogenesis. However, there...
Background/Objectives In recent years, oxytocin (OXT) and polymorphisms in the oxytocin receptor (OXTR) gene have been reported to play roles in obesity...
Background/ObjectivesIn recent years, oxytocin (OXT) and polymorphisms in the oxytocin receptor (OXTR) gene have been reported to play roles in obesity...
SourceID proquest
gale
pubmed
crossref
springer
SourceType Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 2064
SubjectTerms 45/77
692/163/2743/393
692/308
Adolescent
Adolescents
Case-Control Studies
Children
Epidemiology
Female
Gene polymorphism
Genetic aspects
Genetic polymorphisms
Genotype & phenotype
Genotypes
Health aspects
Health Promotion and Disease Prevention
Hormone receptors
Humans
Hyperphagia
Hyperphagia - blood
Hyperphagia - complications
Internal Medicine
Leptin
Male
Medicine
Medicine & Public Health
Metabolic Diseases
Mutants
Obesity
Obesity in adolescence
Oxytocin
Oxytocin - analysis
Oxytocin - blood
Pathogenesis
Pediatric Obesity - blood
Pediatric Obesity - complications
Pediatric research
Polymorphism
Polymorphism, Genetic
Public Health
Receptors
Receptors, Oxytocin - genetics
Risk factors
Teenagers
Title Oxytocin receptor gene polymorphism and low serum oxytocin level are associated with hyperphagia and obesity in adolescents
URI https://link.springer.com/article/10.1038/s41366-021-00876-5
https://www.ncbi.nlm.nih.gov/pubmed/34091593
https://www.proquest.com/docview/2563365026
https://www.proquest.com/docview/2538044744
Volume 45
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfR1db9Mw0IJNQrwgKF-BMYyE4AGixbETO0-oHasmpBWEmNS3yHacUSlNypIKJv48Z8dp10nspXnIXRrnvn3nO4TeRpIpSVMTgqniIVMRDWWiSJjpqKBERal2Gd2zWXp6zr7Mk7nfcGt9WeWgE52iLhpt98iPwDRTCu5EnH5a_Qrt1CibXfUjNO6ifdu6zJZ08Tnflngk0aaXFLUTeYauiGD1E3-CJqLiqAVNntpaXIisbYu2MNmxUjd19TVjdSN76ozS9CF64L1JPO7J_wjdMfUIBZ8XpsPvsG_5WeHZ0HF_hO6d-Vz6CI22HiMAu2nn7WP09-ufqw4IVmNQhWYFETkGFjN41VRXywaIsmiXWNYFrprfGNh3vcTNgFHZAiQsLw2WnuimwHajF_-EaBdw5cVCOuSmH0eAAelaS6kn6Hx68uP4NPQDGkLNOO3CQhtCuM4UMUyDMCeihO_M49KQVMeilBkviYwzycvSGKqpiEtagssjk0xB4EWfor26qc1zhBUzoF60yCRRTCiWyaQQRjNFMmaLAwJEBoLk2ncvt0M0qtxl0anIeyLmQMTcETFPAvRhg7Pqe3fcCv3a0jnvz59uBD8fpxyCUkGjLEDvHYQVffhvLf0JBliBbaK1A3mwAwkiq3dvD7yUe5XR5lsGD9CbzW2LacvgatOsLQwVEWOcwfd41vPgZmUUInXwTWmAPg5MuX34_5f94vZ3eYnux04ubFXdAdrrLtfmFbhhnTp0sga_4pgcov3xdDKZwXVyMvv2_R9U_C4h
linkProvider ProQuest
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEB6VVAIuCMLLUOgi8TiAVdu7fh0QKrRVSpuAUCv1tuyu1xDJsUPsqET8J34js34kTSV669kzttfz7Tw8szMALx3BpKCBttFUhTaTDrWFL107Vk5CXekEqs7oDkfB4JR9PvPPNuBvdxbGlFV2OrFW1EmhzD_yHTTNlKI74QUfpr9sMzXKZFe7ERoNLI704hxDtvL94R7K95XnHeyffBrY7VQBW7GQVnaitOuGKpauZgoR6EepQ2nopdoNlBelIg5TV3ixCNNUa6po5KU0RTst_FhitEDxvjdgk1EMZXqw-XF_9PXbqqjEd5bdq6iZAdT1YUQ_w2_P7Dg02inRdgSm-hdjedMUzvbX7OJl63DBPF7K19Zm8OAu3Gn9V7LbAO4ebOi8D9beWFfkNWmbjGZk1PX478PNYZu970N_5aMicT1fvbwPf778XlQIkZyg8tXTqpgRBLUm0yJbTAqEwbicEJEnJCvOCW6Y-YQUHUdmSp6ImGkiWpjphJhfy-QnxtfIK36MRc1cNAMQCDJdaGL1AE6vRXgPoZcXuX4MRDKNCk1FsXAliySLhZ9EWjHpxsyUI1jgdgLhqu2XbsZ2ZLzO29OIN0LkKEReC5H7Frxd8kybbiFXUm8bOfPmxOtS1fDdIMQwOKJObMGbmsIoG3y2Eu2ZCVyBadu1Rrm1RolKQq1f7rDEWyVV8tWWsuDF8rLhNIV3uS7mhoZGDmMhw-_xqMHgcmWUobPpx9SCdx0oVzf__7KfXP0u23BrcDI85seHo6OncNur94ip6duCXjWb62foBFbyebvzCHy_7s3-D8t9aMM
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV3db9MwELfGkCZeEJSvwGBG4uMBosaxHScPCE2UamOs8MCkvhnbcaBSm5Q21aj4z_jrOOer6yT2tufcJXHudx_One8QehEophWNrA-uSvhMB9RXXBM_MUFKiQ4iU2V0T0fR0Rn7NObjHfS3PQvjyipbm1gZ6rQw7h95H1wzpRBOhFE_a8oivg6G7-e_fDdBymVa23EaNURO7Poctm_Ld8cDkPXLMBx-_PbhyG8mDPiGCVr6qbGECJNoYpkBNPI4CygVYWZJZMI4U4nIiAoTJbLMWmpoHGY0A5-teKJh50DhvjfQTUE5cTomxmJTXsKDro8VddOA2o6MEHHw5vROQOP-ErxI5OqAYVfv2sP5fMtDXvYTFxzlpcxt5RCHd9DtJpLFhzX07qIdm_eQN5jYEr_CTbvRKR613f57aO-0yeP3UG8TrQJxNWl9eQ_9-fJ7XQJYcgxm2M7LYoEB3hbPi-l6VgAgJssZVnmKp8U5BtVZzXDRckxd8RNWC4tVAzibYveTGf-EnTbwqh8TVTEX9SgEDEwX2lndR2fXIroHaDcvcvsIYc0smDYTJ4poFmuWKJ7G1jBNEuYKEzxEWoFI03ROdwM8prLK4NNY1kKUIERZCVFyD73peOZ135ArqQ-cnGV99rUzOvIwErAhjmmQeOh1ReHMDjzbqOb0BKzANfDaotzfogRzYbYvt1iSjblayo1yeeh5d9lxuhK83BYrR0PjgDHB4Hs8rDHYrYwyCDt5Qj30tgXl5ub_X_bjq9_lAO2BisvPx6OTJ-hWWKmIK-7bR7vlYmWfQjRY6meV2mH0_br1_B_Pp2uT
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Oxytocin+receptor+gene+polymorphism+and+low+serum+oxytocin+level+are+associated+with+hyperphagia+and+obesity+in+adolescents&rft.jtitle=International+journal+of+obesity+%282005%29&rft.au=%C3%87atli%2C+G%C3%B6n%C3%BCl&rft.au=Acar%2C+Sezer&rft.au=Cing%C3%B6z%2C+G%C3%BClten&rft.au=Rasulova%2C+Khayala&rft.date=2021-09-01&rft.eissn=1476-5497&rft.volume=45&rft.issue=9&rft.spage=2064&rft_id=info:doi/10.1038%2Fs41366-021-00876-5&rft_id=info%3Apmid%2F34091593&rft.externalDocID=34091593
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0307-0565&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0307-0565&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0307-0565&client=summon