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An intron SNP rs2069837 in IL-6 is associated with osteonecrosis of the femoral head development

BACKGROUND: Genetic polymorphisms play a crucial role in the development of osteonecrosis of the femoral head (ONFH). This study mainly explored the association of IL-6 variants and ONFH susceptibility among the Chinese Han population. METHODS: Two variants (rs2069837, and rs13306435) in the IL-6 ge...

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Autores principales: Wang, Ruisong, Li, Rui, Liu, Ruiyu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734317/
https://www.ncbi.nlm.nih.gov/pubmed/34986839
http://dx.doi.org/10.1186/s12920-021-01142-3
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author Wang, Ruisong
Li, Rui
Liu, Ruiyu
author_facet Wang, Ruisong
Li, Rui
Liu, Ruiyu
author_sort Wang, Ruisong
collection PubMed
description BACKGROUND: Genetic polymorphisms play a crucial role in the development of osteonecrosis of the femoral head (ONFH). This study mainly explored the association of IL-6 variants and ONFH susceptibility among the Chinese Han population. METHODS: Two variants (rs2069837, and rs13306435) in the IL-6 gene were identified and genotyped from 566 patients with ONFH and 566 healthy controls. The associations between IL-6 polymorphisms and ONFH susceptibility were assessed using odds ratio (OR) and 95% confidence interval (95% CI) via logistic regression. The potential function of these two variants was predicted by the HaploReg online database. RESULTS: The results of the overall analysis revealed that IL-6 rs2069837 was correlated with decreased risk of ONFH among the Chinese Han population (p < 0.05). In stratified analysis, rs2069837 also reduced the susceptibility to ONFH in older people (> 51 years), males, nonsmokers, and nondrinkers (p < 0.05). However, no associations between rs13306435 and ONFH susceptibility were observed (p > 0.05). CONCLUSIONS: To sum up, we suggested that rs2069837 G>A polymorphism in the IL-6 gene was significantly associated with a decreased risk of ONFH among the Chinese Hans. These findings underscored the crucial role of IL-6 rs2069837 in the occurrence of ONFH. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-021-01142-3.
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spelling pubmed-87343172022-01-07 An intron SNP rs2069837 in IL-6 is associated with osteonecrosis of the femoral head development Wang, Ruisong Li, Rui Liu, Ruiyu BMC Med Genomics Research BACKGROUND: Genetic polymorphisms play a crucial role in the development of osteonecrosis of the femoral head (ONFH). This study mainly explored the association of IL-6 variants and ONFH susceptibility among the Chinese Han population. METHODS: Two variants (rs2069837, and rs13306435) in the IL-6 gene were identified and genotyped from 566 patients with ONFH and 566 healthy controls. The associations between IL-6 polymorphisms and ONFH susceptibility were assessed using odds ratio (OR) and 95% confidence interval (95% CI) via logistic regression. The potential function of these two variants was predicted by the HaploReg online database. RESULTS: The results of the overall analysis revealed that IL-6 rs2069837 was correlated with decreased risk of ONFH among the Chinese Han population (p < 0.05). In stratified analysis, rs2069837 also reduced the susceptibility to ONFH in older people (> 51 years), males, nonsmokers, and nondrinkers (p < 0.05). However, no associations between rs13306435 and ONFH susceptibility were observed (p > 0.05). CONCLUSIONS: To sum up, we suggested that rs2069837 G>A polymorphism in the IL-6 gene was significantly associated with a decreased risk of ONFH among the Chinese Hans. These findings underscored the crucial role of IL-6 rs2069837 in the occurrence of ONFH. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12920-021-01142-3. BioMed Central 2022-01-05 /pmc/articles/PMC8734317/ /pubmed/34986839 http://dx.doi.org/10.1186/s12920-021-01142-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wang, Ruisong
Li, Rui
Liu, Ruiyu
An intron SNP rs2069837 in IL-6 is associated with osteonecrosis of the femoral head development
title An intron SNP rs2069837 in IL-6 is associated with osteonecrosis of the femoral head development
title_full An intron SNP rs2069837 in IL-6 is associated with osteonecrosis of the femoral head development
title_fullStr An intron SNP rs2069837 in IL-6 is associated with osteonecrosis of the femoral head development
title_full_unstemmed An intron SNP rs2069837 in IL-6 is associated with osteonecrosis of the femoral head development
title_short An intron SNP rs2069837 in IL-6 is associated with osteonecrosis of the femoral head development
title_sort intron snp rs2069837 in il-6 is associated with osteonecrosis of the femoral head development
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734317/
https://www.ncbi.nlm.nih.gov/pubmed/34986839
http://dx.doi.org/10.1186/s12920-021-01142-3
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