Irina Kerna, Kalle Kisand, Ann E Tamm, Jaanika Kumm, Agu O Tamm
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引用次数: 22
Abstract
Objectives. To investigate associations of selected single-nucleotide polymorphisms (SNPs) in ADAM12 gene with radiographic knee osteoarthritis (rKOA) in Estonian population. Methods. The rs3740199, rs1871054, rs1278279, and rs1044122 SNPs in ADAM12 gene 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 of ADAM12 was associated with osteophytosis, again mostly in TFJ in males (P = 0.014). For rs3740199 and rs1278279, no statistically significant associations were observed. Conclusion. ADAM12 gene 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.
目标。目的:探讨ADAM12基因中选择的单核苷酸多态性(snp)与爱沙尼亚人群放射性膝骨关节炎(rKOA)的关系。方法。对438名受试者(303名女性)进行了ADAM12基因的rs3740199、rs1871054、rs1278279和rs1044122 snp基因分型,这些受试者年龄为32 - 57岁(平均45.4岁)。评估胫骨股骨关节(TFJ)和髌骨股骨关节的rKOA特征。结果。51.4%的调查对象(72%的妇女)发现早期rKOA, 12.3%的参与者(63%的妇女)发现疾病晚期。同义SNP rs1044122的A等位基因与TFJ的早期rKOA相关,主要与女性骨赘的存在相关(OR 1.57;95% ci 1.08-2.29, p = 0.018)。内含子多态性rs1871054的C等位基因携带晚期rKOA风险,主要与男性TFJ骨赘形成有关(OR 3.03;95% ci 1.11-7.53, p = 0.018)。ADAM12的CCAA单倍型与骨赘病相关,同样主要发生在男性的TFJ中(P = 0.014)。rs3740199和rs1278279无统计学意义。结论。ADAM12基因变异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,骨赘是骨重塑和新软骨形成的标志。