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Correlation of EYS polymorphisms with lumbar disc herniation risk among Han Chinese population

BACKGROUND: Lumbar disc herniation (LDH) is a common spinal disease in clinical practice. Once lumbar disc herniation occurs, it seriously reduces patient's quality of life. The EYS (eyes shut homolog) was discovered in recent years and it may be related to lumbar disc herniation. So we conduct...

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Autores principales: Ji, Demin, Xing, Wenhua, Li, Feng, Huang, Zhi, Zheng, Wenkai, Hu, Baoyang, Niu, FangLin, Zhu, Yong, Yang, Xuejun
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/PMC6732306/
https://www.ncbi.nlm.nih.gov/pubmed/31359629
http://dx.doi.org/10.1002/mgg3.890
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author Ji, Demin
Xing, Wenhua
Li, Feng
Huang, Zhi
Zheng, Wenkai
Hu, Baoyang
Niu, FangLin
Zhu, Yong
Yang, Xuejun
author_facet Ji, Demin
Xing, Wenhua
Li, Feng
Huang, Zhi
Zheng, Wenkai
Hu, Baoyang
Niu, FangLin
Zhu, Yong
Yang, Xuejun
author_sort Ji, Demin
collection PubMed
description BACKGROUND: Lumbar disc herniation (LDH) is a common spinal disease in clinical practice. Once lumbar disc herniation occurs, it seriously reduces patient's quality of life. The EYS (eyes shut homolog) was discovered in recent years and it may be related to lumbar disc herniation. So we conducted a case–control study to explore the relationship between EYS polymorphism and lumbar disc herniation risk. METHODS: We selected 5 single‐nucleotide polymorphisms (SNPs) of EYS gene in a case–control study with 508 cases and 508 healthy controls to evaluate the relatedness by using genetic model, haplotype, and stratification analysis. RESULTS: We found that the minor alleles of rs62413038 (OR = 1.21, 95%CI: 1.01–1.43, p = .036) and rs9450607 (OR = 1.26, 95% CI: 1.05–1.53, p = .016) were associated with an increased risk of lumbar disc herniation in the allelic model analysis. In the genotypic model analysis, rs62413038 displayed a significantly increased risk of lumbar disc herniation in log‐additive models (OR = 1.20, 95% CI: 1.01–1.43, p = .039). While the rs9450607 was also obviously associated with an increased lumbar disc herniation risk in recessive (OR = 1.98, 95% CI: 1.24–3.13, p = .004) and log‐additive models (OR = 1.27, 95% CI: 1.05–1.55, p = .014). In addition, in the haplotype analyses of the SNPs, we found that the “CGGA” haplotype of rs1482456, rs9342097, rs9450607, and rs7757884 was associated with lumbar disc herniation. (OR = 0.52, 95% CI: 0.30–0.89, p = .017). CONCLUSION: These results suggest that EYS polymorphism may be associated with lumbar disc herniation among Han Chinese population. It also opens up a new exploration direction for the etiology of lumbar disc herniation.
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spelling pubmed-67323062019-09-12 Correlation of EYS polymorphisms with lumbar disc herniation risk among Han Chinese population Ji, Demin Xing, Wenhua Li, Feng Huang, Zhi Zheng, Wenkai Hu, Baoyang Niu, FangLin Zhu, Yong Yang, Xuejun Mol Genet Genomic Med Original Articles BACKGROUND: Lumbar disc herniation (LDH) is a common spinal disease in clinical practice. Once lumbar disc herniation occurs, it seriously reduces patient's quality of life. The EYS (eyes shut homolog) was discovered in recent years and it may be related to lumbar disc herniation. So we conducted a case–control study to explore the relationship between EYS polymorphism and lumbar disc herniation risk. METHODS: We selected 5 single‐nucleotide polymorphisms (SNPs) of EYS gene in a case–control study with 508 cases and 508 healthy controls to evaluate the relatedness by using genetic model, haplotype, and stratification analysis. RESULTS: We found that the minor alleles of rs62413038 (OR = 1.21, 95%CI: 1.01–1.43, p = .036) and rs9450607 (OR = 1.26, 95% CI: 1.05–1.53, p = .016) were associated with an increased risk of lumbar disc herniation in the allelic model analysis. In the genotypic model analysis, rs62413038 displayed a significantly increased risk of lumbar disc herniation in log‐additive models (OR = 1.20, 95% CI: 1.01–1.43, p = .039). While the rs9450607 was also obviously associated with an increased lumbar disc herniation risk in recessive (OR = 1.98, 95% CI: 1.24–3.13, p = .004) and log‐additive models (OR = 1.27, 95% CI: 1.05–1.55, p = .014). In addition, in the haplotype analyses of the SNPs, we found that the “CGGA” haplotype of rs1482456, rs9342097, rs9450607, and rs7757884 was associated with lumbar disc herniation. (OR = 0.52, 95% CI: 0.30–0.89, p = .017). CONCLUSION: These results suggest that EYS polymorphism may be associated with lumbar disc herniation among Han Chinese population. It also opens up a new exploration direction for the etiology of lumbar disc herniation. John Wiley and Sons Inc. 2019-07-30 /pmc/articles/PMC6732306/ /pubmed/31359629 http://dx.doi.org/10.1002/mgg3.890 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/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Ji, Demin
Xing, Wenhua
Li, Feng
Huang, Zhi
Zheng, Wenkai
Hu, Baoyang
Niu, FangLin
Zhu, Yong
Yang, Xuejun
Correlation of EYS polymorphisms with lumbar disc herniation risk among Han Chinese population
title Correlation of EYS polymorphisms with lumbar disc herniation risk among Han Chinese population
title_full Correlation of EYS polymorphisms with lumbar disc herniation risk among Han Chinese population
title_fullStr Correlation of EYS polymorphisms with lumbar disc herniation risk among Han Chinese population
title_full_unstemmed Correlation of EYS polymorphisms with lumbar disc herniation risk among Han Chinese population
title_short Correlation of EYS polymorphisms with lumbar disc herniation risk among Han Chinese population
title_sort correlation of eys polymorphisms with lumbar disc herniation risk among han chinese population
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6732306/
https://www.ncbi.nlm.nih.gov/pubmed/31359629
http://dx.doi.org/10.1002/mgg3.890
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