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首页> 外文期刊>Spine >The TRP2 allele of COL9A2 is an age-dependent risk factor for the development and severity of intervertebral disc degeneration.
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The TRP2 allele of COL9A2 is an age-dependent risk factor for the development and severity of intervertebral disc degeneration.

机译:COL9A2的TRP2等位基因是椎间盘退变的发展和严重程度的年龄依赖性危险因素。

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STUDY DESIGN: Low back pain (LBP) and sciatica are usually caused by degenerative disc disease (DDD). Although they are common, the etiology of these conditions is poorly understood. A large population case-control study in the Southern Chinese was performed to study genetic risk factors to DDD. OBJECTIVES: To gain a better understanding of the etiology of DDD in relation to structural defects of the intervertebral disc. SUMMARY OF BACKGROUND DATA: A Finnish study found an association between LBP and sciatica with two variants of the alpha-chains of collagen IX, encoded by the Trp2 and Trp3 alleles, representing Gln326Trp and Arg103Trp amino acid substitutions in the COL9A2 and COL9A3 genes, respectively. Trp2 was found only in affected individuals (4%), whereas Trp3 was present in both affected (24%) and unaffected (9%) individuals. Because of the low frequency of the Trp2 allele in whites, the significance and contribution of this allele to DDD are not known. Using more objective criteria to define the disease by magnetic resonance imaging (MRI), we tested these alleles for association with DDD in a large population study. METHODS: Lumbar DDD, the presence of anular tears, and disc and endplate herniations were defined by MRI in 804 Southern Chinese volunteers 18 to 55 years of age. These were correlated with the frequencies of the Trp2 and Trp3 alleles. RESULTS: The Trp2 allele was present in 20% of the population and was associated with a fourfold increase in the risk of developing anular tears at 30 to 39 years and a 2.4-fold increase in the risk of developing DDD and endplate herniations at 40 to 49 years. Affected Trp2 individuals had more severe degeneration. The Trp3 allele was absent from the Southern Chinese population. CONCLUSION: This largest-ever population study using MRI to define DDD demonstrates for the first time that the Trp2 allele is a significant risk factor for the development and severity of degeneration. The association is age- dependent as it is more prevalent in some age groups than in others. The contrasting Trp allele frequencies between the Finns and the Chinese are the first indication that the genetic risk factors for DDD varies between ethnic groups.
机译:研究设计:下腰痛(LBP)和坐骨神经痛通常由变性椎间盘疾病(DDD)引起。尽管它们很常见,但对这些疾病的病因知之甚少。在华南地区进行了一项大规模的病例对照研究,以研究DDD的遗传危险因素。目的:为了更好地了解DDD与椎间盘结构缺陷有关的病因。背景数据汇总:一项芬兰研究发现LBP和坐骨神经痛与胶原蛋白IX的两个α链变体之间存在关联,该变体由Trp2和Trp3等位基因编码,分别代表COL9A2和COL9A3基因中的Gln326Trp和Arg103Trp氨基酸取代。 。仅在受影响的个体(4%)中发现了Trp2,而在受影响的个体(24%)和未受影响的个体(9%)中都存在Trp3。由于白人中Trp2等位基因的频率较低,因此未知该等位基因对DDD的重要性和贡献。使用更客观的标准通过磁共振成像(MRI)定义疾病,我们在大量人群研究中测试了这些等位基因与DDD的关联。方法:通过MRI对804名年龄在18至55岁的华南志愿者中的MRI定义了腰椎DDD,肛门撕裂以及椎间盘和终板的突出。这些与Trp2和Trp3等位基因的频率相关。结果:Trp2等位基因存在于20%的人群中,与30-39岁时发生肛门撕裂的风险增加了四倍,而DDD和终板突出症在40-200岁发生的风险增加了2.4倍相关。 49年受影响的Trp2个体具有更严重的变性。 Trp3等位基因不在中国南方人群中。结论:这项有史以来规模最大的人群研究,使用MRI定义DDD,首次证明Trp2等位基因是导致变性和严重性的重要危险因素。该关联是与年龄相关的,因为它在某些年龄组中比在其他年龄组中更普遍。芬兰人和中国人之间Trp等位基因频率的对比是第一个迹象,表明DDD的遗传风险因素在不同种族之间有所不同。

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