Genetic polymorphism of KIAA1217 is functionally associated with lumbar disc herniation in the Chinese population

IF 1.5 4区 医学 Q4 CLINICAL NEUROLOGY Neurochirurgie Pub Date : 2024-02-02 DOI:10.1016/j.neuchi.2024.101538
Jian Dai, Haitao Jiang, Zhang Cheng, Yao Li, Xiaoming Tang
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Abstract

Background

Genetic polymorphism of KIAA1217 has been reported to be associated with lumbar disc herniation (LDH) in different populations such as Japanese population and Finnish population. This study aimed to explore whether the genetic polymorphism of KIAA1217 is functionally associated with LDH in Chinese population.

Methods

SNP rs16924573 of KIAA1217 was genotyped in 1272 patients and 1248 healthy controls. The mRNA expression of KIAA1217 in the intervertebral disc was analyzed for 84 patients and 32 controls. The differences of genotype and allele distributions between LDH patients and healthy controls were evaluated using the Chi-square test. One-way ANOVA test was used to compare the relationship between genotypes and tissue expression of KIAA1217.

Results

Patients were found to have significantly higher frequency of genotype GG of rs16924573 than the controls (64.2% vs. 52.8%, p < 0.001). The frequency of allele G was remarkably higher in the patients than in the controls (79.8% vs. 73.2%, p < 0.001), with an OR of 1.45 (95% confidential interval = 1.27–1.66). Compared with the controls, LDH patients were observed to have significantly decreased expression of KIAA1217. Patients with genotype GG had remarkably lower mRNA expression of KIAA1217 than those with genotype AG or AA (p = 0.01).

Conclusions

SNP rs16924573 of KIAA1217 could be functionally associated with LDH in the Chinese population. More in vivo and vitro experiments need to be carried out to further clarify the regulatory mechanism of functional variants in KIAA1217.

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KIAA1217 基因多态性与中国人群腰椎间盘突出症的功能相关性
背景据报道,KIAA1217的遗传多态性在不同人群中与腰椎间盘突出症(LDH)有关,如日本人群和芬兰人群。本研究旨在探讨中国人群中 KIAA1217 的基因多态性是否与 LDH 功能相关。分析了 84 名患者和 32 名对照组中 KIAA1217 在椎间盘中的 mRNA 表达。采用Chi-square检验评估了LDH患者和健康对照组之间基因型和等位基因分布的差异。结果发现,患者的 rs16924573 基因型 GG 频率明显高于对照组(64.2% vs. 52.8%,p < 0.001)。患者等位基因 G 的频率明显高于对照组(79.8% 对 73.2%,p < 0.001),OR 值为 1.45(95% 置信区间 = 1.27 -1.66 )。与对照组相比,LDH 患者的 KIAA1217 表达明显减少。结论在中国人群中,KIAA1217的SNP rs16924573可能与LDH有功能相关性。要进一步阐明 KIAA1217 功能变异的调控机制,还需要进行更多的体内和体外实验。
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来源期刊
Neurochirurgie
Neurochirurgie 医学-临床神经学
CiteScore
2.70
自引率
6.20%
发文量
100
审稿时长
29 days
期刊介绍: Neurochirurgie publishes articles on treatment, teaching and research, neurosurgery training and the professional aspects of our discipline, and also the history and progress of neurosurgery. It focuses on pathologies of the head, spine and central and peripheral nervous systems and their vascularization. All aspects of the specialty are dealt with: trauma, tumor, degenerative disease, infection, vascular pathology, and radiosurgery, and pediatrics. Transversal studies are also welcome: neuroanatomy, neurophysiology, neurology, neuropediatrics, psychiatry, neuropsychology, physical medicine and neurologic rehabilitation, neuro-anesthesia, neurologic intensive care, neuroradiology, functional exploration, neuropathology, neuro-ophthalmology, otoneurology, maxillofacial surgery, neuro-endocrinology and spine surgery. Technical and methodological aspects are also taken onboard: diagnostic and therapeutic techniques, methods for assessing results, epidemiology, surgical, interventional and radiological techniques, simulations and pathophysiological hypotheses, and educational tools. The editorial board may refuse submissions that fail to meet the journal''s aims and scope; such studies will not be peer-reviewed, and the editor in chief will promptly inform the corresponding author, so as not to delay submission to a more suitable journal. With a view to attracting an international audience of both readers and writers, Neurochirurgie especially welcomes articles in English, and gives priority to original studies. Other kinds of article - reviews, case reports, technical notes and meta-analyses - are equally published. Every year, a special edition is dedicated to the topic selected by the French Society of Neurosurgery for its annual report.
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