Department of Bone and Joint Surgery, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Department of Orthopedics, Luoyang Central Hospital Affiliated to Zhengzhou University, Luoyang, China.
Genet Test Mol Biomarkers. 2020 Dec;24(12):771-776. doi: 10.1089/gtmb.2020.0119. Epub 2020 Nov 12.
Osteoarthritis (OA) is a complex joint disorder characterized by sclerosis of subchondral bone. The knee is one of the most commonly affected joints. Given that the genetic mechanisms underlying knee OA remain elusive, our study aims were to first confirm the association of the gene alleles with the risk of knee OA and, second, to evaluate the relationship between peripheral TGFA concentrations and knee OA in an independent Han Chinese population. We performed a case-control study consisting of 392 knee OA patients and 808 unrelated healthy controls. Single-marker-based association analyses and haplotype-based analyses using 3 single nucleotide polymorphisms (SNPs) were performed to confirm the association of gene alleles with the risk of knee OA. Furthermore, we used enzyme-linked immunosorbent assay (ELISA) kits to detect the peripheral blood TGFA concentrations in patients and healthy controls and then evaluated the relationships between the TGFA alleles and genotypes with serum TGFA levels. We replicated the genetic association of the rs2862851 T allele with the risk of knee OA ( = 1.68 × 10, = 1.41). Moreover, we observed that the peripheral TGFA concentrations were higher in knee OA patients than in healthy controls ( = 8.15 × 10). The peripheral TGFA concentrations were significantly different among the various rs2862851 genotypes for both cases ( = 4.16 × 10) and controls ( = 7.24 × 10). The individuals with the TT genotype in both cases and controls, had the highest peripheral TGFA concentrations. Moreover, with the increase in knee OA grade, peripheral TGFA concentration also increased ( = 1.36 × 10). Our study confirmed the association of the gene with the risk of knee OA and identified a positive correlation between peripheral TGFA levels and the severity of knee OA in the Han Chinese population, providing clues for understanding the etiology of knee OA.
骨关节炎(OA)是一种复杂的关节疾病,其特征为软骨下骨硬化。膝关节是最常受影响的关节之一。由于膝骨关节炎的遗传机制仍不清楚,我们的研究目的首先是确认基因等位基因与膝骨关节炎风险的关联,其次是在独立的汉族人群中评估外周 TGFA 浓度与膝骨关节炎的关系。
我们进行了一项病例对照研究,纳入 392 名膝骨关节炎患者和 808 名无关的健康对照。使用 3 个单核苷酸多态性(SNP)进行基于单标记的关联分析和基于单体型的分析,以确认基因等位基因与膝骨关节炎风险的关联。此外,我们使用酶联免疫吸附试验(ELISA)试剂盒检测患者和健康对照者外周血 TGFA 浓度,然后评估 TGFA 等位基因和基因型与血清 TGFA 水平之间的关系。
我们复制了 rs2862851 T 等位基因与膝骨关节炎风险的遗传关联( = 1.68 × 10, = 1.41)。此外,我们观察到膝骨关节炎患者的外周 TGFA 浓度高于健康对照者( = 8.15 × 10)。对于病例( = 4.16 × 10)和对照( = 7.24 × 10),rs2862851 不同基因型之间的外周 TGFA 浓度存在显著差异。病例和对照中 TT 基因型个体的外周 TGFA 浓度最高。此外,随着膝骨关节炎严重程度的增加,外周 TGFA 浓度也随之升高( = 1.36 × 10)。
我们的研究证实了基因与膝骨关节炎风险的关联,并在汉族人群中发现了外周 TGFA 水平与膝骨关节炎严重程度之间的正相关,为理解膝骨关节炎的病因提供了线索。