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首页> 外文期刊>Spine >MRI Phenotyping of COL9A2/Trp2 and COL9A3/Trp3 Alleles in Lumbar Disc Disease: A Case-control Study in South-Western Iranian Population Reveals a Significant Trp3-Disease Association in Males
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MRI Phenotyping of COL9A2/Trp2 and COL9A3/Trp3 Alleles in Lumbar Disc Disease: A Case-control Study in South-Western Iranian Population Reveals a Significant Trp3-Disease Association in Males

机译:腰椎间盘疾病中COL9A2 / Trp2和COL9A3 / Trp3等位基因的MRI表型:伊朗西南部人群的病例对照研究揭示了男性中显着的Trp3-疾病关联。

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Study Design.A case-control study of the Trp2/3 alleles of COL9A2/3 genes and their correlation with occurrence of Lumbar disc disease (DDD) as phenotyped by magnetic resonance imaging.Objective.To establish a better understanding of relationship between presence of said alleles and occurrence of DDD in South-Western Iranian population.Summary of Background Data.A number of genetic predisposing factors have been identified in elevating the risk of developing DDD. Specifically, the Trp2 and Trp3 alleles of COL9A2 and COL9A3 genes have been suggested as DDD risk variants.Methods.A total of 108 patients (mean age=4111.8 yrs, range=20-66 yrs) with 57 controls (mean age=3510.0 yrs, range=20-58 yrs) participated in the study. The frequency of G/A polymorphism in COL9A2 gene on location 326 on chromosome 1 and G/A/C/ or T polymorphism in 103 location of COL9A3 gene on chromosome 20 was assessed using a PCR short-primer technique. Outcome measure was defined as presence of DDD on MRI. Odds ratios (OR) and 95% confidence intervals (CI) were used to assess the likelihood of DDD given occurrence of Trp2(3).Results.Each allele was present in both patients and controls. The Trp2 allele was positive in 28.5% of individuals (31.5% of patients; 22.8% of controls), OR 1.55 (0.71-3.56). The Trp3 allele, the frequency was 23.6% in all patients (26.9% patients; 17.5% controls), OR 1.72 (0.73-4.33). We observed a 5.8-fold increase in the odds of DDD in males when the Trp3 allele was present, OR 5.83 (1.09-9.98), P=0.0273.Conclusion.Both Trp2 and Trp3 alleles occurred more frequently compared with other studied ethnicities. The sampled Iranian population exhibited a similar Trp2 frequency to a Southern Chinese population, and Trp3 occurrence to Finnish and Greek population. We found that male patient were much more likely to develop DDD when Trp 3 was present.Level of Evidence: N/A
机译:研究设计:通过磁共振成像对COL9A2 / 3基因的Trp2 / 3等位基因及其与腰椎间盘疾病(DDD)发生的相关性进行病例对照研究。伊朗西南部人群中存在DDD等位基因和DDD的发生。背景数据摘要。已鉴定出许多遗传易感因素,可增加DDD发生的风险。具体来说,已建议将COL9A2和COL9A3基因的Trp2和Trp3等位基因作为DDD风险变体。 ,范围= 20-58岁)参加了这项研究。使用PCR短引物技术评估了COL9A2基因在1号染色体上326位的G / A多态性的频率和COL9A3基因在20号染色体上103位的G / A / C /或T多态性的频率。结果测量被定义为MRI上DDD的存在。在出现Trp2(3)的情况下,使用比值比(OR)和95%置信区间(CI)评估DDD的可能性。结果:患者和对照中均存在每个等位基因。 Trp2等位基因在28.5%的个体(31.5%的患者; 22.8%的对照)中呈阳性,或1.55(0.71-3.56)。 Trp3等位基因在所有患者中占23.6%(26.9%患者; 17.5%对照),或1.72(0.73-4.33)。我们发现当存在Trp3等位基因时,男性DDD的几率增加了5.8倍,或5.83(1.09-9.98),P = 0.0273。结论。与其他研究种族相比,Trp2和Trp3等位基因的发生频率更高。抽样的伊朗人口展示的Trp2频率与华南人口相似,Trp3的发生与芬兰和希腊人口相似。我们发现当存在Trp 3时,男性患者更有可能发展DDD。证据水平:N / A

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