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The alpha2 type IX collagen tryptophan polymorphism is associated with the severity of disc degeneration in younger patients with herniated nucleus pulposus of the lumbar spine

机译:在较年轻的腰椎髓核突出患者中α2型IX胶原蛋白色氨酸多态性与椎间盘退变的严重程度有关

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摘要

Tryptophan alleles in COL9A2 (Trp2) and COL9A3 (Trp3) have been linked to lumbar disc diseases in the Finnish population. Although such diseases consist of various pathogenetically different conditions, detailed analysis of each has not been well documented. The aim of this study was to clarify whether the collagen IX tryptophan alleles influence the symptomatic degeneration of the lumbar disc in Japanese patients with herniated nucleus pulposus. We performed a prospective study of 84 patients who underwent lumbar discectomy. The degree of disc degeneration was evaluated by magnetic resonance images in relation to the collagen IX genotype. Twenty patients (21.4%) had the Trp2 allele and no patients had the Trp3 allele. Patients under 40 years with the Trp2 allele showed more severe disc degeneration at the surgical level than did those without the Trp2 allele (odds ratio 6.00, P=0.043). In contrast, patients aged 40 years or over did not show significant association between disc degeneration and collagen IX genotype. Our results suggest that the Trp2 allele is an age-dependent risk factor for the severity of disc degeneration in younger patients with symptomatic herniated nucleus pulposus of the lumbar spine.
机译:在芬兰人群中,COL9A2(Trp2)和COL9A3(Trp3)中的色氨酸等位基因与腰椎间盘疾病有关。尽管此类疾病由各种病原学上不同的条件组成,但每种疾病的详细分析尚未得到充分记录。这项研究的目的是弄清楚胶原蛋白IX色氨酸等位基因是否影响日本髓核突出患者的腰椎间盘症状性退化。我们对84位接受了腰椎间盘切除术的患者进行了一项前瞻性研究。通过与IX型胶原基因型相关的磁共振图像评估椎间盘退变的程度。二十名患者(21.4%)患有Trp2等位基因,无患者患有Trp3等位基因。患有Trp2等位基因的40岁以下患者与没有Trp2等位基因的患者相比,在手术水平上显示出更严重的椎间盘退变(优势比6.00,P = 0.043)。相比之下,40岁或以上的患者并没有显示椎间盘退变与IX型胶原基因型之间的显着相关性。我们的结果表明,Trp2等位基因是年轻的腰椎有症状椎间盘突出髓核年轻患者椎间盘退变严重程度的年龄依赖性危险因素。

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