Sports Research Centre, Miguel Hernandez University of Elche, Alicante, Spain.
Exercise Physiology Laboratory, Camilo José Cela University, Madrid, Spain.
PLoS One. 2020 Jan 28;15(1):e0227548. doi: 10.1371/journal.pone.0227548. eCollection 2020.
A common single nucleotide polymorphism in the ACTN3 gene might result in the complete deficiency of α-actinin-3 (i.e., XX genotype). It has been found that ACTN3 XX individuals have several traits related to lessened muscle performance. This study aimed to determine the influence, if any, of ACTN3 genotypes on injury incidence of marathoners during the year preceding to participating in a competitive marathon race. Using a cross-sectional experimental design, the type and conditions of sports injuries were documented for one year in a group of 139 marathoners. Injuries were recorded following a consensus statement on injuries in Athletics. Afterward, ACTN3 genotyping was performed, and injury epidemiology was compared among RR, RX, and XX genotypes. The distribution of the RR/RX/XX genotypes was 28.8/42.8/23.5%, respectively. A total of 67 injuries were recorded. The frequency of marathoners that reported any injury during the previous year was not different across the genotypes (55.0/38.8/40.6%, P = 0.241). Although the overall injury incidence was not different among genotypes (2.78/1.65/1.94 injuries/1000 h of running, P = 0.084), the likelihood of suffering an injury was higher in RR than in RX (OR = 1.93: 95%CI = 0.87-4.30), and higher than in XX (OR = 1.79: 0.70-4.58). There was no difference in the conditions, severity, body location, time of year, or leading cause of injury among genotypes. However, XX presented a higher frequency of sudden-onset injuries (P = 0.024), and the OR for muscle-type injuries was 2.0 (0.51-7.79) times higher compared to RR runners. Although XX marathoners did not have a higher overall incidence of injury, the OR in these runners for muscle-type injuries was superior to RR and RX runners. The likelihood of suffering a muscle injury, especially with a sudden-onset, was twice in XX than in RR endurance runners.
一种常见的 ACTN3 基因单核苷酸多态性可能导致 α-辅肌动蛋白-3(即 XX 基因型)完全缺失。已经发现,ACTN3 XX 个体具有与肌肉性能降低相关的多种特征。本研究旨在确定 ACTN3 基因型对参加竞技马拉松比赛前一年马拉松运动员受伤发生率的影响。使用横断面实验设计,对 139 名马拉松运动员的一年中运动损伤的类型和情况进行了记录。损伤是根据田径运动损伤的共识声明记录的。随后,进行了 ACTN3 基因分型,并比较了 RR、RX 和 XX 基因型之间的损伤流行病学。RR/RX/XX 基因型的分布分别为 28.8/42.8/23.5%。共记录了 67 例损伤。前一年报告任何损伤的马拉松运动员的频率在基因型之间没有差异(55.0/38.8/40.6%,P=0.241)。尽管基因型之间的总体损伤发生率没有差异(2.78/1.65/1.94 例/1000 小时跑步,P=0.084),但 RR 发生损伤的可能性高于 RX(OR=1.93:95%CI=0.87-4.30),也高于 XX(OR=1.79:0.70-4.58)。基因型之间的损伤情况、严重程度、身体位置、一年中的时间或受伤的主要原因没有差异。然而,XX 组突发损伤的频率较高(P=0.024),肌肉型损伤的 OR 为 2.0(0.51-7.79)倍高于 RR 跑者。尽管 XX 马拉松运动员总体受伤发生率没有增加,但这些运动员肌肉型损伤的 OR 优于 RR 和 RX 跑者。XX 耐力跑者发生肌肉损伤的可能性是 RR 耐力跑者的两倍,尤其是突发损伤的可能性。