Department of Dental Prosthetics, Pomeranian Medical University, 70-111 Szczecin, Poland.
Department of Genetics and Pathology, Pomeranian Medical University, 70-111 Szczecin, Poland.
Cells. 2021 Sep 14;10(9):2423. doi: 10.3390/cells10092423.
Numerous reports describe the association between the single-nucleotide polymorphism (SNP) rs12722 and rs13946 in the gene and injuries, such as Achilles tendon pathology, anterior cruciate ligament (ACL) injuries, and tennis elbow. Hence, there were no studies investigating and temporomandibular joint (TMJ) pathology. The aim of this study is to evaluate the relationship between rs12722 and rs13946 SNPs and TMJ articular disc displacement without reduction (ADDwoR). In this case-control study, the study group consisted of 124 Caucasian patients of both sexes. Each patient had a history of ADDwoR no more than 3 months prior. The control group comprised 126 patients with no signs of TMD according to DC/TMD. Genotyping of the selected SNPs was performed by real-time PCR using TaqMan probes. The significance of the differences in the distribution of genotypes was analyzed using Pearson's chi-square test. Logistic regression modeling was performed to analyze the influence of the 164 investigated SNPs on ADDwoR. The marker rs12722 turned out to be statistically significant (-value = 0.0119), implying that there is a difference in the frequencies of TMJ ADDwoR. The distribution of rs12722 SNPs in the study group TT(66), CC(27), CT(31) vs. control group TT(45), CC(26), CT(51) indicates that patients with CT had an almost 2.4 times higher likelihood of ADDwoR (OR = 2.41) than those with reference TT (OR = 1), while rs13946 genotypes were shown to be insignificant, with a -value of 0.1713. The rs12722 polymorphism is a risk factor for ADDwoR in the Polish Caucasian population.
许多报告描述了基因中的单核苷酸多态性 (SNP) rs12722 和 rs13946 与损伤之间的关联,例如跟腱病变、前交叉韧带 (ACL) 损伤和网球肘。因此,没有研究调查颞下颌关节 (TMJ) 病理学。本研究旨在评估 rs12722 和 rs13946SNP 与 TMJ 关节盘无复位 (ADDwoR) 之间的关系。在这项病例对照研究中,研究组包括 124 名男女白种人患者。每位患者均有 3 个月内发生 ADDwoR 的病史。对照组由 126 名根据 DC/TMD 无 TMD 迹象的患者组成。使用 TaqMan 探针通过实时 PCR 对选定的 SNPs 进行基因分型。使用 Pearson 卡方检验分析基因型分布差异的显著性。进行逻辑回归建模,以分析 164 个调查 SNP 对 ADDwoR 的影响。标记 rs12722 结果具有统计学意义(-值 = 0.0119),表明 TMJ ADDwoR 的频率存在差异。研究组中 rs12722 SNP 的分布 TT(66)、CC(27)、CT(31)与对照组 TT(45)、CC(26)、CT(51)表明,CT 患者发生 ADDwoR 的可能性几乎是 TT 参考患者的 2.4 倍(OR = 2.41),而 rs13946 基因型则无统计学意义,-值为 0.1713。rs12722 多态性是波兰白种人群 ADDwoR 的危险因素。