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Association of Adiponectin rs1501299 and rs266729 Gene Polymorphisms With Nonalcoholic Fatty Liver Disease

BACKGROUND: Genetic and environmental factors are important for the development of nonalcoholic fatty liver disease (NAFLD). Adiponectin is a white and brown adipose tissue hormone, and have been found to play essential roles in the regulation of energy homoeostasis. Recent reports have identified a...

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Autores principales: Hashemi, Mohammad, Hanafi Bojd, Hamideh, Eskandari Nasab, Ebrahim, Bahari, Ali, Hashemzehi, Noor Allah, Shafieipour, Sara, Narouie, Behzad, Taheri, Mohsen, Ghavami, Saeid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Kowsar 2013
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734897/
https://www.ncbi.nlm.nih.gov/pubmed/23922565
http://dx.doi.org/10.5812/hepatmon.9527
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author Hashemi, Mohammad
Hanafi Bojd, Hamideh
Eskandari Nasab, Ebrahim
Bahari, Ali
Hashemzehi, Noor Allah
Shafieipour, Sara
Narouie, Behzad
Taheri, Mohsen
Ghavami, Saeid
author_facet Hashemi, Mohammad
Hanafi Bojd, Hamideh
Eskandari Nasab, Ebrahim
Bahari, Ali
Hashemzehi, Noor Allah
Shafieipour, Sara
Narouie, Behzad
Taheri, Mohsen
Ghavami, Saeid
author_sort Hashemi, Mohammad
collection PubMed
description BACKGROUND: Genetic and environmental factors are important for the development of nonalcoholic fatty liver disease (NAFLD). Adiponectin is a white and brown adipose tissue hormone, and have been found to play essential roles in the regulation of energy homoeostasis. Recent reports have identified a possible role of adiponectin in NAFLD via PPARγ pathway. OBJECTIVES: The present study was designed to find out the impact of adiponectin rs1501299 (276G/T) and rs266729 (-11377C/G) gene polymorphisms in NAFLD. PATIENTS AND METHODS: Eighty-three patients with diagnosis of NAFLD, and 93 healthy subjects were included in the study. Tetra ARMS-PCR was designed to detect single nucleotide polymorphisms. RESULTS: A significant difference was found between NAFLD and control group regarding the rs266729 polymorphism (χ2 = 7.35, P = 0.025). The rs266729 polymorphism increased the risk of NAFLD in codominant (CC vs. CG: OR = 2.18, 95% CI = 1.16 - 4.12, P = 0.016) and dominant (CC vs. CG/GG: OR = 2.31, 95% CI = 1.25 - 4.27; P = 0.008) inheritance tested models. The G allele increased the risk of NAFLD (OR = 1.63, 95% CI = 1.03 - 2.57, P = 0.037) in comparison with C allele. No significant difference was found between the groups concerning adiponectin rs1501299 gene polymorphism (χ2 = 0.70, P = 0.697). CONCLUSIONS: adiponectin rs266729 polymorphism might be a candidate gene, which determines the susceptibility to NAFLD. Larger studies are necessary to confirm these findings in various populations.
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spelling pubmed-37348972013-08-06 Association of Adiponectin rs1501299 and rs266729 Gene Polymorphisms With Nonalcoholic Fatty Liver Disease Hashemi, Mohammad Hanafi Bojd, Hamideh Eskandari Nasab, Ebrahim Bahari, Ali Hashemzehi, Noor Allah Shafieipour, Sara Narouie, Behzad Taheri, Mohsen Ghavami, Saeid Hepat Mon Research Article BACKGROUND: Genetic and environmental factors are important for the development of nonalcoholic fatty liver disease (NAFLD). Adiponectin is a white and brown adipose tissue hormone, and have been found to play essential roles in the regulation of energy homoeostasis. Recent reports have identified a possible role of adiponectin in NAFLD via PPARγ pathway. OBJECTIVES: The present study was designed to find out the impact of adiponectin rs1501299 (276G/T) and rs266729 (-11377C/G) gene polymorphisms in NAFLD. PATIENTS AND METHODS: Eighty-three patients with diagnosis of NAFLD, and 93 healthy subjects were included in the study. Tetra ARMS-PCR was designed to detect single nucleotide polymorphisms. RESULTS: A significant difference was found between NAFLD and control group regarding the rs266729 polymorphism (χ2 = 7.35, P = 0.025). The rs266729 polymorphism increased the risk of NAFLD in codominant (CC vs. CG: OR = 2.18, 95% CI = 1.16 - 4.12, P = 0.016) and dominant (CC vs. CG/GG: OR = 2.31, 95% CI = 1.25 - 4.27; P = 0.008) inheritance tested models. The G allele increased the risk of NAFLD (OR = 1.63, 95% CI = 1.03 - 2.57, P = 0.037) in comparison with C allele. No significant difference was found between the groups concerning adiponectin rs1501299 gene polymorphism (χ2 = 0.70, P = 0.697). CONCLUSIONS: adiponectin rs266729 polymorphism might be a candidate gene, which determines the susceptibility to NAFLD. Larger studies are necessary to confirm these findings in various populations. Kowsar 2013-05-21 /pmc/articles/PMC3734897/ /pubmed/23922565 http://dx.doi.org/10.5812/hepatmon.9527 Text en Copyright © 2013, Kowsar Corp. http://creativecommons.org/licenses/by/3/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hashemi, Mohammad
Hanafi Bojd, Hamideh
Eskandari Nasab, Ebrahim
Bahari, Ali
Hashemzehi, Noor Allah
Shafieipour, Sara
Narouie, Behzad
Taheri, Mohsen
Ghavami, Saeid
Association of Adiponectin rs1501299 and rs266729 Gene Polymorphisms With Nonalcoholic Fatty Liver Disease
title Association of Adiponectin rs1501299 and rs266729 Gene Polymorphisms With Nonalcoholic Fatty Liver Disease
title_full Association of Adiponectin rs1501299 and rs266729 Gene Polymorphisms With Nonalcoholic Fatty Liver Disease
title_fullStr Association of Adiponectin rs1501299 and rs266729 Gene Polymorphisms With Nonalcoholic Fatty Liver Disease
title_full_unstemmed Association of Adiponectin rs1501299 and rs266729 Gene Polymorphisms With Nonalcoholic Fatty Liver Disease
title_short Association of Adiponectin rs1501299 and rs266729 Gene Polymorphisms With Nonalcoholic Fatty Liver Disease
title_sort association of adiponectin rs1501299 and rs266729 gene polymorphisms with nonalcoholic fatty liver disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3734897/
https://www.ncbi.nlm.nih.gov/pubmed/23922565
http://dx.doi.org/10.5812/hepatmon.9527
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