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Association of adiponectin gene polymorphisms with knee osteoarthritis
AIM: To investigate the possible relationship of adiponectin (ADIPOQ) gene polymorphisms, plasma adiponectin, and the risk of knee osteoarthritis (OA). METHODS: A total of 398 subjects, 202 knee OA patients and 196 healthy individuals, were enrolled in the case-control study. Genotyping at +45T/G (r...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Baishideng Publishing Group Inc
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605358/ https://www.ncbi.nlm.nih.gov/pubmed/28979856 http://dx.doi.org/10.5312/wjo.v8.i9.719 |
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author | Zhan, Dong Thumtecho, Suthimon Tanavalee, Aree Yuktanandana, Pongsak Anomasiri, Wilai Honsawek, Sittisak |
author_facet | Zhan, Dong Thumtecho, Suthimon Tanavalee, Aree Yuktanandana, Pongsak Anomasiri, Wilai Honsawek, Sittisak |
author_sort | Zhan, Dong |
collection | PubMed |
description | AIM: To investigate the possible relationship of adiponectin (ADIPOQ) gene polymorphisms, plasma adiponectin, and the risk of knee osteoarthritis (OA). METHODS: A total of 398 subjects, 202 knee OA patients and 196 healthy individuals, were enrolled in the case-control study. Genotyping at +45T/G (rs2241766) and +276G/T (rs1501299) loci was performed using polymerase chain reaction-restriction fragment length polymorphism. Plasma adiponectin levels were assessed using enzyme-linked immunosorbent assay. OA severity was determined using the Kellgren-Lawrence (KL) grading system. RESULTS: No significant associations were observed in the genotype distributions and allele frequencies at two loci of +45T/G and +276G/T polymorphisms in the ADIPOQ between knee OA patients and control subjects. There was a significant association between genotype distribution of +276G/T polymorphism and KL grade 2, 3 or 4 (P = 0.037, P = 0.046, P = 0.016, respectively). At +45T/G locus, the percentage of GG genotype was notably greater in control subjects (13.40%) compared with OA subjects (1.70%) (P = 0.023). Plasma adiponectin was markedly decreased in OA subjects compared with control subjects (P = 0.03). Likewise, circulating adiponectin in OA subjects was notably lesser than that in control subjects in GG genotype of +45T/G (P = 0.029) and +276G/T polymorphisms (P = 0.012). CONCLUSION: Polymorphisms +45T/G and +276G/T of the ADIPOQ gene might not be responsible for OA susceptibility among Thais. |
format | Online Article Text |
id | pubmed-5605358 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Baishideng Publishing Group Inc |
record_format | MEDLINE/PubMed |
spelling | pubmed-56053582017-10-04 Association of adiponectin gene polymorphisms with knee osteoarthritis Zhan, Dong Thumtecho, Suthimon Tanavalee, Aree Yuktanandana, Pongsak Anomasiri, Wilai Honsawek, Sittisak World J Orthop Prospective Study AIM: To investigate the possible relationship of adiponectin (ADIPOQ) gene polymorphisms, plasma adiponectin, and the risk of knee osteoarthritis (OA). METHODS: A total of 398 subjects, 202 knee OA patients and 196 healthy individuals, were enrolled in the case-control study. Genotyping at +45T/G (rs2241766) and +276G/T (rs1501299) loci was performed using polymerase chain reaction-restriction fragment length polymorphism. Plasma adiponectin levels were assessed using enzyme-linked immunosorbent assay. OA severity was determined using the Kellgren-Lawrence (KL) grading system. RESULTS: No significant associations were observed in the genotype distributions and allele frequencies at two loci of +45T/G and +276G/T polymorphisms in the ADIPOQ between knee OA patients and control subjects. There was a significant association between genotype distribution of +276G/T polymorphism and KL grade 2, 3 or 4 (P = 0.037, P = 0.046, P = 0.016, respectively). At +45T/G locus, the percentage of GG genotype was notably greater in control subjects (13.40%) compared with OA subjects (1.70%) (P = 0.023). Plasma adiponectin was markedly decreased in OA subjects compared with control subjects (P = 0.03). Likewise, circulating adiponectin in OA subjects was notably lesser than that in control subjects in GG genotype of +45T/G (P = 0.029) and +276G/T polymorphisms (P = 0.012). CONCLUSION: Polymorphisms +45T/G and +276G/T of the ADIPOQ gene might not be responsible for OA susceptibility among Thais. Baishideng Publishing Group Inc 2017-09-18 /pmc/articles/PMC5605358/ /pubmed/28979856 http://dx.doi.org/10.5312/wjo.v8.i9.719 Text en ©The Author(s) 2017. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ Open-Access: This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Prospective Study Zhan, Dong Thumtecho, Suthimon Tanavalee, Aree Yuktanandana, Pongsak Anomasiri, Wilai Honsawek, Sittisak Association of adiponectin gene polymorphisms with knee osteoarthritis |
title | Association of adiponectin gene polymorphisms with knee osteoarthritis |
title_full | Association of adiponectin gene polymorphisms with knee osteoarthritis |
title_fullStr | Association of adiponectin gene polymorphisms with knee osteoarthritis |
title_full_unstemmed | Association of adiponectin gene polymorphisms with knee osteoarthritis |
title_short | Association of adiponectin gene polymorphisms with knee osteoarthritis |
title_sort | association of adiponectin gene polymorphisms with knee osteoarthritis |
topic | Prospective Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5605358/ https://www.ncbi.nlm.nih.gov/pubmed/28979856 http://dx.doi.org/10.5312/wjo.v8.i9.719 |
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