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The OXTR Polymorphism Stratified the Correlation of Oxytocin and Glucose Homeostasis in Non-Diabetic Subjects

OBJECTIVE: Previous animal studies have shown that the oxytocin system might affect glucose homeostasis through the hypothalamus–pituitary–adrenal (HPA) axis and peripheral organs. Moreover, whether the effect is stratified by the polymorphism of oxytocin receptor gene (OXTR) remains unclear. METHOD...

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Autores principales: Chang, Hui Hua, Chang, Wei Hung, Chi, Mei Hung, Peng, Yi Chin, Huang, Chih-Chun, Yang, Yen Kuang, Chen, Po See
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927562/
https://www.ncbi.nlm.nih.gov/pubmed/31908511
http://dx.doi.org/10.2147/DMSO.S226245
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author Chang, Hui Hua
Chang, Wei Hung
Chi, Mei Hung
Peng, Yi Chin
Huang, Chih-Chun
Yang, Yen Kuang
Chen, Po See
author_facet Chang, Hui Hua
Chang, Wei Hung
Chi, Mei Hung
Peng, Yi Chin
Huang, Chih-Chun
Yang, Yen Kuang
Chen, Po See
author_sort Chang, Hui Hua
collection PubMed
description OBJECTIVE: Previous animal studies have shown that the oxytocin system might affect glucose homeostasis through the hypothalamus–pituitary–adrenal (HPA) axis and peripheral organs. Moreover, whether the effect is stratified by the polymorphism of oxytocin receptor gene (OXTR) remains unclear. METHODS: In this study, we recruited 89 non-diabetic participants. Their plasma oxytocin and serum insulin profiles were obtained, and the polymorphism of OXTR rs53576 was genotyped. RESULTS: There were significant correlations between the oxytocin level and fasting glucose level (r = –0.29, P <0.01), insulin level (r = –0.26, P = 0.01), and homeostasis model assessment-estimated insulin resistance (HOMA-IR) (r = –0.25, P = 0.01), when adjusted for age, gender, and body mass index (BMI). When further considering the stratification effects of OXTR variation, we found that the oxytocin level was significantly correlated with the fasting glucose level (r = –0.25, P = 0.04), insulin level (r = –0.35, P = 0.03), and HOMA-IR (r = –0.35, P < 0.01) in subjects with the OXTR A allele (n = 75) after adjustment for age, gender, and BMI. In addition, the oxytocin level in those with the GG genotype of OXTR was significantly negatively correlated with the leptin level (n = 14, r = –0.66, P = 0.02). CONCLUSION: The results demonstrated that the polymorphism of OXTR plays an important role in individual differences in the correlation of oxytocin and glucose homeostasis in non-diabetic subjects.
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spelling pubmed-69275622020-01-06 The OXTR Polymorphism Stratified the Correlation of Oxytocin and Glucose Homeostasis in Non-Diabetic Subjects Chang, Hui Hua Chang, Wei Hung Chi, Mei Hung Peng, Yi Chin Huang, Chih-Chun Yang, Yen Kuang Chen, Po See Diabetes Metab Syndr Obes Original Research OBJECTIVE: Previous animal studies have shown that the oxytocin system might affect glucose homeostasis through the hypothalamus–pituitary–adrenal (HPA) axis and peripheral organs. Moreover, whether the effect is stratified by the polymorphism of oxytocin receptor gene (OXTR) remains unclear. METHODS: In this study, we recruited 89 non-diabetic participants. Their plasma oxytocin and serum insulin profiles were obtained, and the polymorphism of OXTR rs53576 was genotyped. RESULTS: There were significant correlations between the oxytocin level and fasting glucose level (r = –0.29, P <0.01), insulin level (r = –0.26, P = 0.01), and homeostasis model assessment-estimated insulin resistance (HOMA-IR) (r = –0.25, P = 0.01), when adjusted for age, gender, and body mass index (BMI). When further considering the stratification effects of OXTR variation, we found that the oxytocin level was significantly correlated with the fasting glucose level (r = –0.25, P = 0.04), insulin level (r = –0.35, P = 0.03), and HOMA-IR (r = –0.35, P < 0.01) in subjects with the OXTR A allele (n = 75) after adjustment for age, gender, and BMI. In addition, the oxytocin level in those with the GG genotype of OXTR was significantly negatively correlated with the leptin level (n = 14, r = –0.66, P = 0.02). CONCLUSION: The results demonstrated that the polymorphism of OXTR plays an important role in individual differences in the correlation of oxytocin and glucose homeostasis in non-diabetic subjects. Dove 2019-12-19 /pmc/articles/PMC6927562/ /pubmed/31908511 http://dx.doi.org/10.2147/DMSO.S226245 Text en © 2019 Chang et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Chang, Hui Hua
Chang, Wei Hung
Chi, Mei Hung
Peng, Yi Chin
Huang, Chih-Chun
Yang, Yen Kuang
Chen, Po See
The OXTR Polymorphism Stratified the Correlation of Oxytocin and Glucose Homeostasis in Non-Diabetic Subjects
title The OXTR Polymorphism Stratified the Correlation of Oxytocin and Glucose Homeostasis in Non-Diabetic Subjects
title_full The OXTR Polymorphism Stratified the Correlation of Oxytocin and Glucose Homeostasis in Non-Diabetic Subjects
title_fullStr The OXTR Polymorphism Stratified the Correlation of Oxytocin and Glucose Homeostasis in Non-Diabetic Subjects
title_full_unstemmed The OXTR Polymorphism Stratified the Correlation of Oxytocin and Glucose Homeostasis in Non-Diabetic Subjects
title_short The OXTR Polymorphism Stratified the Correlation of Oxytocin and Glucose Homeostasis in Non-Diabetic Subjects
title_sort oxtr polymorphism stratified the correlation of oxytocin and glucose homeostasis in non-diabetic subjects
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6927562/
https://www.ncbi.nlm.nih.gov/pubmed/31908511
http://dx.doi.org/10.2147/DMSO.S226245
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