Cargando…

The effect of SOX4 gene 3′UTR polymorphisms on osteoporosis

OBJECTIVE: This study aimed to explore the correlation between the SRY-related high-mobility-group box gene 4 (SOX4) 3′ untranslated region (UTR) single nucleotide polymorphism (SNP) and osteoporosis susceptibility. METHODS: The study recruited 330 osteoporosis patients (the case group) and 330 non-...

Descripción completa

Detalles Bibliográficos
Autores principales: Li, Guo, Gu, Zuchao, He, Yue, Wang, Chongwen, Duan, JiQiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130251/
https://www.ncbi.nlm.nih.gov/pubmed/34006298
http://dx.doi.org/10.1186/s13018-021-02454-x
_version_ 1783694476742492160
author Li, Guo
Gu, Zuchao
He, Yue
Wang, Chongwen
Duan, JiQiang
author_facet Li, Guo
Gu, Zuchao
He, Yue
Wang, Chongwen
Duan, JiQiang
author_sort Li, Guo
collection PubMed
description OBJECTIVE: This study aimed to explore the correlation between the SRY-related high-mobility-group box gene 4 (SOX4) 3′ untranslated region (UTR) single nucleotide polymorphism (SNP) and osteoporosis susceptibility. METHODS: The study recruited 330 osteoporosis patients (the case group) and 330 non-osteoporosis patients (the control group) in Sichuan Chengdu First People’s Hospital and Zibo Central Hospital from August 2016 to August 2019. Sanger sequencing was used to analyze the genotypes of SOX4 gene rs79958549, rs139085828, and rs201335371 loci. Multi-factor dimensionality reduction (MDR) was used to analyze the interaction between the SOX4 gene rs79958549, rs139085828, and rs201335371 loci and the clinical characteristics of the subjects. RESULTS: The risk of osteoporosis in the carriers of A allele at SOX4 rs79958549 was 5.40 times that in the carriers of the G allele (95% CI 3.25–8.96, P < 0.01). The risk of osteoporosis in the carriers of the A allele at SOX4 rs139085828 was 1.68 times that in the carriers of the G allele (95% CI 1.45–1.85, P < 0.01). The risk of osteoporosis in the carriers of the T allele at SOX4 rs201335371 was 0.54 times that in the carriers of the C allele (95% CI 0.43–0.69, P < 0.01). The SOX4 gene rs79958549, rs139085828, and rs201335371 A-A-C haplotype (OR = 5.14, 95% CI 2.45–10.57, P < 0.01) were associated with increased risk of osteoporosis and G-G-T haplotype was significantly associated with decreased risk of osteoporosis (OR = 0.48, 95% CI 0.38–0.62, P < 0.01). The interaction among the factors of sex, smoking, drinking, rs79958549, rs201335371 was the best model for osteoporosis prediction, and the risk for osteoporosis in ‘high-risk combination’ was 2.74 times that of ‘low-risk combination’ (95% CI 1.01–7.43, P = 0.04). Multiple logistic regression analysis revealed that the risk factors for osteoporosis were BMD (OR = 5.85, 95% CI 2.88–8.94, P < 0.01), T score (OR = 8.54, 95% CI 5.66–10.49, P < 0.01), Z score (OR = 3.77, 95% CI 2.15–8.50, P < 0.01), rs79958549 SNP (OR = 6.92, 95% CI 3.58–8.93, P < 0.01), and rs139085828 SNP (OR = 2.36, 95% CI 1.85–4.27, P < 0.01). The protective factor for osteoporosis was rs201335371SNP (OR = 0.48, 95% CI 0.32–0.75, P < 0.01). CONCLUSION: The SOX4 gene SNPs rs79958549, rs139085828, and rs201335371 loci were significantly associated with osteoporosis risk.
format Online
Article
Text
id pubmed-8130251
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-81302512021-05-18 The effect of SOX4 gene 3′UTR polymorphisms on osteoporosis Li, Guo Gu, Zuchao He, Yue Wang, Chongwen Duan, JiQiang J Orthop Surg Res Research Article OBJECTIVE: This study aimed to explore the correlation between the SRY-related high-mobility-group box gene 4 (SOX4) 3′ untranslated region (UTR) single nucleotide polymorphism (SNP) and osteoporosis susceptibility. METHODS: The study recruited 330 osteoporosis patients (the case group) and 330 non-osteoporosis patients (the control group) in Sichuan Chengdu First People’s Hospital and Zibo Central Hospital from August 2016 to August 2019. Sanger sequencing was used to analyze the genotypes of SOX4 gene rs79958549, rs139085828, and rs201335371 loci. Multi-factor dimensionality reduction (MDR) was used to analyze the interaction between the SOX4 gene rs79958549, rs139085828, and rs201335371 loci and the clinical characteristics of the subjects. RESULTS: The risk of osteoporosis in the carriers of A allele at SOX4 rs79958549 was 5.40 times that in the carriers of the G allele (95% CI 3.25–8.96, P < 0.01). The risk of osteoporosis in the carriers of the A allele at SOX4 rs139085828 was 1.68 times that in the carriers of the G allele (95% CI 1.45–1.85, P < 0.01). The risk of osteoporosis in the carriers of the T allele at SOX4 rs201335371 was 0.54 times that in the carriers of the C allele (95% CI 0.43–0.69, P < 0.01). The SOX4 gene rs79958549, rs139085828, and rs201335371 A-A-C haplotype (OR = 5.14, 95% CI 2.45–10.57, P < 0.01) were associated with increased risk of osteoporosis and G-G-T haplotype was significantly associated with decreased risk of osteoporosis (OR = 0.48, 95% CI 0.38–0.62, P < 0.01). The interaction among the factors of sex, smoking, drinking, rs79958549, rs201335371 was the best model for osteoporosis prediction, and the risk for osteoporosis in ‘high-risk combination’ was 2.74 times that of ‘low-risk combination’ (95% CI 1.01–7.43, P = 0.04). Multiple logistic regression analysis revealed that the risk factors for osteoporosis were BMD (OR = 5.85, 95% CI 2.88–8.94, P < 0.01), T score (OR = 8.54, 95% CI 5.66–10.49, P < 0.01), Z score (OR = 3.77, 95% CI 2.15–8.50, P < 0.01), rs79958549 SNP (OR = 6.92, 95% CI 3.58–8.93, P < 0.01), and rs139085828 SNP (OR = 2.36, 95% CI 1.85–4.27, P < 0.01). The protective factor for osteoporosis was rs201335371SNP (OR = 0.48, 95% CI 0.32–0.75, P < 0.01). CONCLUSION: The SOX4 gene SNPs rs79958549, rs139085828, and rs201335371 loci were significantly associated with osteoporosis risk. BioMed Central 2021-05-18 /pmc/articles/PMC8130251/ /pubmed/34006298 http://dx.doi.org/10.1186/s13018-021-02454-x Text en © The Author(s) 2021 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 Article
Li, Guo
Gu, Zuchao
He, Yue
Wang, Chongwen
Duan, JiQiang
The effect of SOX4 gene 3′UTR polymorphisms on osteoporosis
title The effect of SOX4 gene 3′UTR polymorphisms on osteoporosis
title_full The effect of SOX4 gene 3′UTR polymorphisms on osteoporosis
title_fullStr The effect of SOX4 gene 3′UTR polymorphisms on osteoporosis
title_full_unstemmed The effect of SOX4 gene 3′UTR polymorphisms on osteoporosis
title_short The effect of SOX4 gene 3′UTR polymorphisms on osteoporosis
title_sort effect of sox4 gene 3′utr polymorphisms on osteoporosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8130251/
https://www.ncbi.nlm.nih.gov/pubmed/34006298
http://dx.doi.org/10.1186/s13018-021-02454-x
work_keys_str_mv AT liguo theeffectofsox4gene3utrpolymorphismsonosteoporosis
AT guzuchao theeffectofsox4gene3utrpolymorphismsonosteoporosis
AT heyue theeffectofsox4gene3utrpolymorphismsonosteoporosis
AT wangchongwen theeffectofsox4gene3utrpolymorphismsonosteoporosis
AT duanjiqiang theeffectofsox4gene3utrpolymorphismsonosteoporosis
AT liguo effectofsox4gene3utrpolymorphismsonosteoporosis
AT guzuchao effectofsox4gene3utrpolymorphismsonosteoporosis
AT heyue effectofsox4gene3utrpolymorphismsonosteoporosis
AT wangchongwen effectofsox4gene3utrpolymorphismsonosteoporosis
AT duanjiqiang effectofsox4gene3utrpolymorphismsonosteoporosis