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首页> 外文期刊>Arthritis >Two Single-Nucleotide Polymorphisms inADAM12Gene Are Associated with Early and Late Radiographic Knee Osteoarthritis in Estonian Population
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Two Single-Nucleotide Polymorphisms inADAM12Gene Are Associated with Early and Late Radiographic Knee Osteoarthritis in Estonian Population

机译:在爱沙尼亚人群中,ADAM12基因的两个单核苷酸多态性与早期和晚期影像学膝关节骨关节炎有关。

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Objectives.To investigate associations of selected single-nucleotide polymorphisms (SNPs) inADAM12gene with radiographic knee osteoarthritis (rKOA) in Estonian population.Methods.The rs3740199, rs1871054, rs1278279, and rs1044122 SNPs inADAM12gene were genotyped in 438 subjects (303 women) from population-based cohort, aged 32 to 57 (mean 45.4). The rKOA features were evaluated in the tibiofemoral joint (TFJ) and patellofemoral joint.Results.The early rKOA was found in 51.4% of investigated subjects (72% women) and 12.3% of participants (63% women) had advanced stage of diseases. The A allele of synonymous SNP rs1044122 was associated with early rKOA in TFJ, predominantly with the presence of osteophytes in females (OR 1.57; 95% CI 1.08–2.29,P=0.018). The C allele of intron polymorphism rs1871054 carried risk for advanced rKOA, mostly to osteophyte formation in TFJ in males (OR 3.03; 95% CI 1.11–7.53,P=0.018). Also the CCAA haplotype ofADAM12was associated with osteophytosis, again mostly in TFJ in males (P=0.014). For rs3740199 and rs1278279, no statistically significant associations were observed.Conclusion.  ADAM12gene variants are related to rKOA risk during the early and late stages of diseases. The genetic risk seems to be predominantly associated with the appearance of osteophytes—a marker of bone remodelling and neochondrogenesis.
机译:目的:研究爱沙尼亚人群ADAM12基因中选定的单核苷酸多态性(SNP)与放射照相的膝关节骨关节炎(rKOA)的关系。年龄在32岁至57岁之间(平均45.4岁)。结果在胫股关节和of股关节中评估了rKOA特征。结果:早期rKOA发现于51.4%的受试者(72%为女性)和12.3%的受试者(63%为女性)处于疾病晚期。同义SNP rs1044122的A等位基因与TFJ中的早期rKOA相关,主要与女性中存在骨赘有关(OR 1.57; 95%CI 1.08–2.29,P = 0.018)。内含子多态性rs1871054的C等位基因具有晚期rKOA的风险,主要存在于男性TFJ中骨赘形成(OR 3.03; 95%CI 1.11–7.53,P = 0.018)。同样,ADAM12的CCAA单倍型也与骨赘形成有关,在男性的TFJ中同样如此(P = 0.014)。对于rs3740199和rs1278279,未观察到统计学上显着的关联。 ADAM12基因变体与疾病早期和晚期的rKOA风险有关。遗传风险似乎主要与骨赘的出现有关,骨赘是骨骼重塑和新软骨形成的标志。

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