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创伤性跟腱断裂患者中纤连蛋白-2和弹性蛋白基因多态性的评估:跟腱断裂是一种遗传性疾病吗?

Assessment of fibrillin-2 and elastin gene polymorphisms in patients with a traumatic Achilles tendon rupture: Is Achilles tendon rupture a genetic disease?

作者信息

Poszepczyński Jan, Pietrusiński Michał, Borowiec Maciej, Edward Domżalski Marcin

机构信息

Department of Orthopedics and Traumatology, Military Medical Academy Memorial Teaching Hospital, Lodz, Poland.

Department of Clinical Genetics, Medical University of Lodz, Lodz, Poland.

出版信息

Acta Orthop Traumatol Turc. 2023 Mar;57(2):73-77. doi: 10.5152/j.aott.2023.22024.

Abstract

OBJECTIVE

The study aimed to investigate the polymorphism of fibrillin-2 (FBN2) and elastin genes in patients with Achilles tendon rupture and to compare the results with a control group of participants who did not experience such an injury.

METHODS

In this prospective study, 106 consecutive patients in whom traumatic Achilles tendon rupture was diagnosed and treated were included. The control group consisted of randomly selected 92 athletes (10 women and 82 men) 85 of whom had practiced sports in the past, aged 40-76 years, who during their sports career did not experience Achilles tendon ruptures. Material for genetic tests was obtained by the swab from the oral cavity epithelium of all the study population.

RESULTS

102 (96%) of patients with traumatic Achilles tendon ruptures were people with polymorphism B or heterozygotes for the elastin gene. 97 (92%) of patients with traumatic Achilles tendon ruptures were people with polymorphism B and heterozygotes for the FBN2 gene. Patients with homozygote A of the elastin gene and homozygote A of the FBN2 gene demonstrated a considerably lower incidence rate of sport-related Achilles tendon rupture. The type of sport that led to the Achilles tendon rupture and the amount of experience practicing it, as well as BMI and drug usage, did not contribute to a higher rate of incidence of any additional musculoskeletal problems or a longer time to return to their pre-injury sports activity. Polymorphisms of the fibrillin 2 (P=.0001) and elastin (P=.0009) genes impact the occurrence of traumatic injury to the Achilles tendon. However, it does not affect the length of full recovery time (P =.2251).

CONCLUSION

Minimally invasive and, above all, safe collection of genetic material from the epithelium of the oral cavity in order to assess the polymorphic state of the FBN and elastin genes may allow the identification of a group of players at risk of Achilles tendon rupture resulting in long-term injury, which will significantly affect their sports career in the future.

LEVEL OF EVIDENCE

Level II, Prognostic Study.

摘要

目的

本研究旨在调查跟腱断裂患者中纤连蛋白-2(FBN2)和弹性蛋白基因的多态性,并将结果与未经历此类损伤的对照组参与者进行比较。

方法

在这项前瞻性研究中,纳入了106例连续诊断并治疗创伤性跟腱断裂的患者。对照组由随机选择的92名运动员(10名女性和82名男性)组成,其中85人过去曾从事体育运动,年龄在40-76岁之间,在其运动生涯中未经历过跟腱断裂。通过拭子从所有研究人群的口腔上皮中获取基因检测材料。

结果

102例(96%)创伤性跟腱断裂患者为弹性蛋白基因B型多态性或杂合子。97例(92%)创伤性跟腱断裂患者为FBN2基因B型多态性和杂合子。弹性蛋白基因纯合子A和FBN2基因纯合子A的患者与运动相关的跟腱断裂发生率明显较低。导致跟腱断裂的运动类型及其练习经验量,以及体重指数和药物使用情况,均未导致任何其他肌肉骨骼问题的发生率升高或恢复到受伤前运动活动所需的时间延长。纤连蛋白2(P = 0.0001)和弹性蛋白(P = 0.0009)基因的多态性影响创伤性跟腱损伤的发生。然而,它并不影响完全恢复时间的长短(P = 0.2251)。

结论

通过微创且最重要的是安全地从口腔上皮收集基因材料以评估FBN和弹性蛋白基因的多态性状态,可能有助于识别一组有跟腱断裂导致长期损伤风险的运动员,这将对他们未来的运动生涯产生重大影响。

证据水平

二级,预后研究。

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