Suppr超能文献

维生素D受体FokI基因多态性和维生素D结合蛋白Thr420Lys基因多态性与脊髓型颈椎病的相关性:一项中国人群的病例对照研究

Association of VDR-FokI and VDBP-Thr420Lys polymorphisms with cervical spondylotic myelopathy: A case-control study in the population of China.

作者信息

Song De-Wei, Wu Yu-Dong, Tian Dong-Dong

机构信息

Department of Pain, the People's Hospital of Mengyin County, Mengyin, China.

出版信息

J Clin Lab Anal. 2019 Feb;33(2):e22669. doi: 10.1002/jcla.22669. Epub 2018 Nov 21.

Abstract

BACKGROUND

Cervical spondylotic myelopathy (CSM), a common degenerative disorder, is characterized by chronic progressive compression of the cervical spinal cord. The present case-control study aimed to explore the potential role of VDR-FokI and VDBP-Thr420Lys polymorphisms in the susceptibility to CSM in the Chinese population.

METHODS

The study enrolled 318 CSM patients and 282 healthy individuals whose clinical data were retrospectively analyzed. Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) analysis was used to genotype VDR-FokI and VDBP-Thr420Lys polymorphisms. The severity of CSM was assessed using the Japanese Orthopaedic Association (JOA) score with magnetic resonance imaging (MRI) of cervical vertebra. A nonconditional binary logistic regression model was conducted for assessing the risk factors of CSM.

RESULTS

Patients in the CSM group had longer time duration to bend over desk working than the control group. The ff genotype and f allele frequency of VDR-FokI were elevated in CSM patients. Elevated Ff + ff genotype and f allele frequency of VDR-FokI might increase the risk of CSM. The VDR-FokI polymorphism was associated with nucleus pulposus capillary invasion, necrosis, hyaline degeneration and fibrosis, genesis and hyperplasia of cartilage-like cells, and fibrocyst in the fibrous ring. The VDR-FokI and VDBP-Thr420Lys genotypes conformed to Hardy-Weinberg equilibrium which showed that VDR-FokI and VDBP-Thr420Lys had group representation characteristics.

CONCLUSION

Binary logistic regression analysis confirmed that VDR-FokI polymorphism and the time to bend over desk working were risk factors of CSM. Our results indicate that VDR-FokI polymorphism may be closely associated with the risk of CSM.

摘要

背景

脊髓型颈椎病(CSM)是一种常见的退行性疾病,其特征为颈椎脊髓的慢性进行性受压。本病例对照研究旨在探讨维生素D受体基因FokI(VDR-FokI)和维生素D结合蛋白基因Thr420Lys(VDBP-Thr420Lys)多态性在中国人群脊髓型颈椎病易感性中的潜在作用。

方法

本研究纳入318例脊髓型颈椎病患者和282例健康个体,对其临床资料进行回顾性分析。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)分析对VDR-FokI和VDBP-Thr420Lys多态性进行基因分型。采用日本骨科学会(JOA)评分结合颈椎磁共振成像(MRI)评估脊髓型颈椎病的严重程度。采用非条件二元logistic回归模型评估脊髓型颈椎病的危险因素。

结果

脊髓型颈椎病组患者伏案工作时间长于对照组。脊髓型颈椎病患者中VDR-FokI的ff基因型和f等位基因频率升高。VDR-FokI的Ff + ff基因型和f等位基因频率升高可能增加脊髓型颈椎病的发病风险。VDR-FokI多态性与髓核毛细血管侵入、坏死、玻璃样变性和纤维化、软骨样细胞的发生和增生以及纤维环中的纤维囊肿有关。VDR-FokI和VDBP-Thr420Lys基因型符合Hardy-Weinberg平衡,表明VDR-FokI和VDBP-Thr420Lys具有群体代表性特征。

结论

二元logistic回归分析证实VDR-FokI多态性和伏案工作时间是脊髓型颈椎病的危险因素。我们的结果表明,VDR-FokI多态性可能与脊髓型颈椎病的发病风险密切相关。

相似文献

2
Effect of osteoprotegerin gene polymorphisms on the risk of cervical spondylotic myelopathy in a Chinese population.
Clin Neurol Neurosurg. 2018 Dec;175:149-154. doi: 10.1016/j.clineuro.2018.09.013. Epub 2018 Sep 8.
3
The genetic association of vitamin D receptor polymorphisms and cervical spondylotic myelopathy in Chinese subjects.
Clin Chim Acta. 2010 Jun 3;411(11-12):794-7. doi: 10.1016/j.cca.2010.01.031. Epub 2010 Feb 6.
4
VDR and VDBP genes polymorphisms associated with susceptibility to tuberculosis in a Han Taiwanese population.
J Microbiol Immunol Infect. 2016 Oct;49(5):783-787. doi: 10.1016/j.jmii.2015.12.008. Epub 2016 Jan 12.
6
Effects of brain derived neurotrophic factor Val66Met polymorphism in patients with cervical spondylotic myelopathy.
J Clin Neurosci. 2016 Feb;24:117-21. doi: 10.1016/j.jocn.2015.07.016. Epub 2015 Oct 10.
10
Vitamin D receptor gene FokI polymorphism in Egyptian children and adolescents with SLE: A case-control study.
Lupus. 2017 Nov;26(13):1426-1434. doi: 10.1177/0961203317725588. Epub 2017 Aug 11.

引用本文的文献

1
Prognostic value of circ_0000043/miR-590-5p in cervical cancer and regulation of tumor progression.
Discov Oncol. 2025 May 23;16(1):879. doi: 10.1007/s12672-025-02670-5.
2
Updates in current concepts in degenerative cervical myelopathy: a systematic review.
J Spine Surg. 2024 Jun 21;10(2):313-326. doi: 10.21037/jss-23-123. Epub 2024 May 7.
3
Evaluation of Genetic and Nongenetic Risk Factors for Degenerative Cervical Myelopathy.
Spine (Phila Pa 1976). 2023 Aug 15;48(16):1117-1126. doi: 10.1097/BRS.0000000000004735. Epub 2023 May 30.
4
Degenerative Cervical Myelopathy: Insights into Its Pathobiology and Molecular Mechanisms.
J Clin Med. 2021 Mar 15;10(6):1214. doi: 10.3390/jcm10061214.

本文引用的文献

2
Genetic factors of cervical spondylotic myelopathy-a systemic review.
J Clin Neurosci. 2017 Oct;44:89-94. doi: 10.1016/j.jocn.2017.06.043. Epub 2017 Jul 19.
4
Regulation of vitamin D receptor expression by retinoic acid receptor alpha in acute myeloid leukemia cells.
J Steroid Biochem Mol Biol. 2016 May;159:121-30. doi: 10.1016/j.jsbmb.2016.03.013. Epub 2016 Mar 8.
6
Vitamin D receptor BsmI polymorphism and osteoporosis risk in post-menopausal women.
Arch Med Sci. 2016 Feb 1;12(1):25-30. doi: 10.5114/aoms.2016.57475. Epub 2016 Jan 27.
7
Effects of brain derived neurotrophic factor Val66Met polymorphism in patients with cervical spondylotic myelopathy.
J Clin Neurosci. 2016 Feb;24:117-21. doi: 10.1016/j.jocn.2015.07.016. Epub 2015 Oct 10.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验