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聚集蛋白聚糖基因串联重复序列可变数目多态性与椎间盘退变之间的关联。

Association between the aggrecan gene variable number of tandem repeats polymorphism and intervertebral disc degeneration.

作者信息

Solovieva Svetlana, Noponen Noora, Männikkö Minna, Leino-Arjas Päivi, Luoma Katariina, Raininko Raili, Ala-Kokko Leena, Riihimäki Hilkka

机构信息

Finnish Institute of Occupational Health, Helsinki, Finland.

出版信息

Spine (Phila Pa 1976). 2007 Jul 15;32(16):1700-5. doi: 10.1097/BRS.0b013e3180b9ed51.

DOI:10.1097/BRS.0b013e3180b9ed51
PMID:17632389
Abstract

STUDY DESIGN

Cross-sectional study.

OBJECTIVE

To examine the association between an aggrecan variable number of tandem repeats (VNTR) polymorphism and intervertebral disc degeneration in middle-aged Finnish men.

SUMMARY OF BACKGROUND DATA

An association between the aggrecan VNTR polymorphism and multilevel disc degeneration has been previously reported in young Japanese women.

METHODS

Lumbar discs of 132 men representing 3 occupations (carpenters, machine drivers, and office workers) were evaluated on magnetic resonance imaging, using decreased signal intensity of the nucleus pulposus, disc bulges, and decreased disc height as signs of degeneration. The aggrecan gene VNTR region was analyzed by Southern hybridization.

RESULTS

The allele A26 with 26 repeats was statistically significantly overrepresented among the persons with dark nucleus pulposus. Carrying 2 copies of the A26 allele increased the risk of dark nucleus pulposus (odds ratio = 2.77; 95% confidence interval, 1.24-6.16). Carrying the alleles with either less or more than 26 repeats decreased the risk of dark nucleus pulposus. The carpenters and machine drivers with the A26 allele had a statistically significantly higher risk of disc bulge and decreased disc height than the office workers without the allele.

CONCLUSION

The findings provide additional support for the role of the aggrecan gene VNTR polymorphism in intervertebral disc degeneration.

摘要

研究设计

横断面研究。

目的

探讨芬兰中年男性中聚集蛋白聚糖可变串联重复序列(VNTR)多态性与椎间盘退变之间的关联。

背景数据总结

此前有报道称,聚集蛋白聚糖VNTR多态性与年轻日本女性的多节段椎间盘退变有关。

方法

对代表3种职业(木匠、机器驾驶员和办公室职员)的132名男性的腰椎间盘进行磁共振成像评估,将髓核信号强度降低、椎间盘膨出和椎间盘高度降低作为退变的征象。通过Southern杂交分析聚集蛋白聚糖基因VNTR区域。

结果

在髓核信号暗的人群中,具有26个重复序列的A26等位基因在统计学上显著过量存在。携带2个拷贝的A26等位基因会增加髓核信号暗的风险(优势比 = 2.77;95%置信区间,1.24 - 6.16)。携带重复序列少于或多于26个的等位基因会降低髓核信号暗的风险。携带A26等位基因的木匠和机器驾驶员比不携带该等位基因的办公室职员发生椎间盘膨出和椎间盘高度降低的风险在统计学上显著更高。

结论

这些发现为聚集蛋白聚糖基因VNTR多态性在椎间盘退变中的作用提供了额外支持。

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