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Significant association between RETN genetic polymorphisms and alcohol‐induced osteonecrosis of femoral head

BACKGROUND: Alcohol‐induced osteonecrosis of femoral head (ONFH) is a complex disease and genetic factors are one of the causes. The purpose of this study is to investigate the effects of RETN (resistin; OMIM: 605565) and LDLR (low density lipoprotein receptor; OMIM: 606945) polymorphisms on the ris...

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Autores principales: Liu, Chang, An, Feimeng, Cao, Yuju, Wang, Jiaqi, Tian, Ye, Wu, Huiqiang, Wang, Jianzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687866/
https://www.ncbi.nlm.nih.gov/pubmed/31207150
http://dx.doi.org/10.1002/mgg3.822
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author Liu, Chang
An, Feimeng
Cao, Yuju
Wang, Jiaqi
Tian, Ye
Wu, Huiqiang
Wang, Jianzhong
author_facet Liu, Chang
An, Feimeng
Cao, Yuju
Wang, Jiaqi
Tian, Ye
Wu, Huiqiang
Wang, Jianzhong
author_sort Liu, Chang
collection PubMed
description BACKGROUND: Alcohol‐induced osteonecrosis of femoral head (ONFH) is a complex disease and genetic factors are one of the causes. The purpose of this study is to investigate the effects of RETN (resistin; OMIM: 605565) and LDLR (low density lipoprotein receptor; OMIM: 606945) polymorphisms on the risk of alcohol‐induced ONFH in Chinese Han population. METHODS: A case–control study including 201 patients and 201 controls was designed. Seven single nucleotide polymorphisms (SNPs) in RETN gene and four SNPs in LDLR gene were genotyped using Agena MassARRAY platform. In allele model and genetic model, chi‐square test and logistic regression were used to study the associations between these SNPs and ONFH susceptibility. In addition, the relationships between these SNPs, clinical phenotypes, and blood lipid level with one‐way analysis of variance were analyzed. RESULTS: In the allele model, rs7408174 and rs3745369 in RETN were associated with increased risk of alcohol‐induced ONFH, whereas rs34861192 and rs3219175 in RETN showed reduced risk of alcohol‐induced ONFH. In the genetic model, rs7408174 was associated with increased risk of alcohol‐induced ONFH in dominant model and log‐additive model. Rs3745369 showed an increased risk in codominant model, recessive model, and log‐additive model. Rs34861192 showed a decreased risk in codominant model, dominant model, and log‐additive model, and rs3219175 showed a decreased risk in dominant model and log‐additive model. The rs3745368 in RETN was associated with the clinical stage of the disease. CONCLUSION: These results suggest that RETN genetic polymorphisms are associated with the susceptibility of alcohol‐induced ONFH in Chinese Han population.
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spelling pubmed-66878662019-08-14 Significant association between RETN genetic polymorphisms and alcohol‐induced osteonecrosis of femoral head Liu, Chang An, Feimeng Cao, Yuju Wang, Jiaqi Tian, Ye Wu, Huiqiang Wang, Jianzhong Mol Genet Genomic Med Original Articles BACKGROUND: Alcohol‐induced osteonecrosis of femoral head (ONFH) is a complex disease and genetic factors are one of the causes. The purpose of this study is to investigate the effects of RETN (resistin; OMIM: 605565) and LDLR (low density lipoprotein receptor; OMIM: 606945) polymorphisms on the risk of alcohol‐induced ONFH in Chinese Han population. METHODS: A case–control study including 201 patients and 201 controls was designed. Seven single nucleotide polymorphisms (SNPs) in RETN gene and four SNPs in LDLR gene were genotyped using Agena MassARRAY platform. In allele model and genetic model, chi‐square test and logistic regression were used to study the associations between these SNPs and ONFH susceptibility. In addition, the relationships between these SNPs, clinical phenotypes, and blood lipid level with one‐way analysis of variance were analyzed. RESULTS: In the allele model, rs7408174 and rs3745369 in RETN were associated with increased risk of alcohol‐induced ONFH, whereas rs34861192 and rs3219175 in RETN showed reduced risk of alcohol‐induced ONFH. In the genetic model, rs7408174 was associated with increased risk of alcohol‐induced ONFH in dominant model and log‐additive model. Rs3745369 showed an increased risk in codominant model, recessive model, and log‐additive model. Rs34861192 showed a decreased risk in codominant model, dominant model, and log‐additive model, and rs3219175 showed a decreased risk in dominant model and log‐additive model. The rs3745368 in RETN was associated with the clinical stage of the disease. CONCLUSION: These results suggest that RETN genetic polymorphisms are associated with the susceptibility of alcohol‐induced ONFH in Chinese Han population. John Wiley and Sons Inc. 2019-06-17 /pmc/articles/PMC6687866/ /pubmed/31207150 http://dx.doi.org/10.1002/mgg3.822 Text en © 2019 The Authors. Molecular Genetics & Genomic Medicine published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles
Liu, Chang
An, Feimeng
Cao, Yuju
Wang, Jiaqi
Tian, Ye
Wu, Huiqiang
Wang, Jianzhong
Significant association between RETN genetic polymorphisms and alcohol‐induced osteonecrosis of femoral head
title Significant association between RETN genetic polymorphisms and alcohol‐induced osteonecrosis of femoral head
title_full Significant association between RETN genetic polymorphisms and alcohol‐induced osteonecrosis of femoral head
title_fullStr Significant association between RETN genetic polymorphisms and alcohol‐induced osteonecrosis of femoral head
title_full_unstemmed Significant association between RETN genetic polymorphisms and alcohol‐induced osteonecrosis of femoral head
title_short Significant association between RETN genetic polymorphisms and alcohol‐induced osteonecrosis of femoral head
title_sort significant association between retn genetic polymorphisms and alcohol‐induced osteonecrosis of femoral head
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687866/
https://www.ncbi.nlm.nih.gov/pubmed/31207150
http://dx.doi.org/10.1002/mgg3.822
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