Udomsinprasert Wanvisa, Yuktanandana Pongsak, Tanpowpong Thanathep, Malila Somkiat, Jiamjarasrangsi Wiroj, Honsawek Sittisak
Department of Biochemistry, Faculty of Pharmacy, Mahidol University, Bangkok 10400.
Vinai Parkpian Orthopaedic Research Center, Department of Orthopaedics.
Biomed Rep. 2019 Feb;10(2):133-139. doi: 10.3892/br.2018.1180. Epub 2018 Dec 31.
Anterior cruciate ligament (ACL) rupture is one the most common musculoskeletal soft tissue injuries of the knee. Although the exact mechanisms of this injury remain uncertain, genetic variants have been considered to be an intrinsic risk factor associated with ACL rupture. Therefore, the aim of the present study was to determine whether the adiponectin +276G/T polymorphism is associated with susceptibility to ACL rupture in a Thai population. Genotyping for rs1501299 was conducted in 98 participants with ACL rupture and 95 healthy controls by polymerase chain reaction-restriction fragment length polymorphism analysis. The results demonstrated that the GG genotype and G allele were significantly associated with an increased risk of ACL rupture [odds ratio (OR)=1.91, P=0.026; OR=1.89, P=0.004], whereas the TT genotype was significantly associated with a reduced risk of ACL rupture (OR=0.32, P=0.019). Furthermore, ACL injury patients with non-contact sports carrying the GG genotype and G allele exhibited a significantly higher risk of ACL rupture (OR=2.13, P=0.031; OR=1.84, P=0.029). In addition, overweight patients carrying the GG genotype and G allele had a significantly increased (8-fold) risk of ACL rupture (OR=8.00, P<0.001; OR=5.15, P<0.001), whereas overweight patients with the adiponectin +276G/T GT genotype had a significantly lower risk of ACL rupture (OR=0.13, P<0.001). Therefore, the adiponectin +276G/T polymorphism GG genotype and G allele were significantly associated with the risk of ACL rupture, particularly in overweight patients. These findings indicate that the adiponectin +276G/T polymorphism may play a role in the development of ACL rupture in the Thai population.
前交叉韧带(ACL)断裂是膝关节最常见的肌肉骨骼软组织损伤之一。尽管这种损伤的确切机制仍不确定,但基因变异被认为是与ACL断裂相关的内在风险因素。因此,本研究的目的是确定脂联素+276G/T多态性是否与泰国人群中ACL断裂的易感性相关。通过聚合酶链反应-限制性片段长度多态性分析,对98例ACL断裂患者和95例健康对照者进行了rs1501299基因分型。结果表明,GG基因型和G等位基因与ACL断裂风险增加显著相关[比值比(OR)=1.91,P=0.026;OR=1.89,P=0.004],而TT基因型与ACL断裂风险降低显著相关(OR=0.32,P=0.019)。此外,携带GG基因型和G等位基因的非接触性运动ACL损伤患者ACL断裂风险显著更高(OR=2.13,P=0.031;OR=1.84,P=0.029)。另外,携带GG基因型和G等位基因的超重患者ACL断裂风险显著增加(8倍)(OR=8.00,P<0.001;OR=5.15,P<0.001),而脂联素+276G/T GT基因型的超重患者ACL断裂风险显著更低(OR=0.13,P<0.001)。因此,脂联素+276G/T多态性的GG基因型和G等位基因与ACL断裂风险显著相关,尤其是在超重患者中。这些发现表明脂联素+276G/T多态性可能在泰国人群ACL断裂的发生中起作用。