Collins Malcolm, Raleigh Stuart M
Med Sport Sci. 2009;54:136-149. doi: 10.1159/000235701. Epub 2009 Aug 17.
Acute and overuse musculoskeletal soft tissues injuries are common as a result of participating in specific physical or workplace activities. Multiple risk factors, including genetic factors, are implicated in the aetiology of these injuries. Common musculoskeletal soft tissue injuries for which a genetic contribution has been proposed include the Achilles tendon in the heel, the rotator cuff tendons in the shoulder and the cruciate ligaments in the knee. Recent developments in the identification of genetic risk factors for tendon and ligament injuries will be reviewed. Sequence variants within genes that encode for several tendon and/or ligament extracellular matrix proteins have been shown to be associated with specific musculoskeletal soft tissues injuries. Variants within the TNC, COL5A1 and MMP3 genes co-segregate with chronic Achilles tendinopathy. The variant within the TNC gene also appears to co-segregate with Achilles tendon ruptures, while sequence variants within the COL1A1 and COL5A1 genes have been shown to be associated with cruciate ligament ruptures and/or shoulder dislocations. Whether these variants are directly involved in the development of these musculoskeletal soft tissue abnormalities or in strong linkage disequilibrium with actual disease-causing loci remains to be established. We proposed that genetic risk factors will in the future be included in multifactorial models developed to understand the molecular mechanisms that cause musculoskeletal soft tissue injuries or related pathology. Clinicians could eventually use these models to develop personalised training programmes to reduce the risk of injury as well as to develop treatment and rehabilitation regimens for the injured individual.
由于参与特定的体育活动或工作场所活动,急性和过度使用性肌肉骨骼软组织损伤很常见。包括遗传因素在内的多种风险因素与这些损伤的病因有关。已提出有遗传因素作用的常见肌肉骨骼软组织损伤包括足跟的跟腱、肩部的肩袖肌腱和膝部的交叉韧带。本文将综述肌腱和韧带损伤遗传风险因素识别方面的最新进展。编码几种肌腱和/或韧带细胞外基质蛋白的基因中的序列变异已被证明与特定的肌肉骨骼软组织损伤有关。TNC、COL5A1和MMP3基因内的变异与慢性跟腱病共分离。TNC基因内的变异似乎也与跟腱断裂共分离,而COL1A1和COL5A1基因内的序列变异已被证明与交叉韧带断裂和/或肩关节脱位有关。这些变异是直接参与这些肌肉骨骼软组织异常的发生发展,还是与实际致病位点存在强连锁不平衡,仍有待确定。我们提出,未来遗传风险因素将被纳入多因素模型,以了解导致肌肉骨骼软组织损伤或相关病理的分子机制。临床医生最终可以使用这些模型来制定个性化的训练计划,以降低受伤风险,并为受伤个体制定治疗和康复方案。