Gruss Magnetic Resonance Imaging Center, Albert Einstein College of Medicine, Montefiore Medical Center, Bronx, New York.
Litwin-Zucker Center for the Study of Alzheimer's Disease, The Feinstein Institute for Medical Research, Northwell Health, Manhasset, New York.
JAMA Neurol. 2020 Apr 1;77(4):419-426. doi: 10.1001/jamaneurol.2019.4828.
Emerging evidence suggests that long-term exposure to ball heading in soccer, the most popular sport in the world, confers risk for adverse cognitive outcomes. However, the extent to which the apolipoprotein E ε4 (APOE ε4) allele, a common risk factor for neurodegeneration, and ball heading are associated with cognition in soccer players remains unknown.
To determine whether the APOE ε4 allele and 12-month ball heading exposure are associated with verbal memory in a cohort of adult amateur soccer players.
DESIGN, SETTINGS, AND PARTICIPANTS: A total of 379 amateur soccer players were enrolled in the longitudinal Einstein Soccer Study from November 11, 2013, through January 23, 2018. Selection criteria included participation in soccer for more than 5 years and for more than 6 months per year. Of the 379 individuals enrolled in the study, 355 were genotyped. Three players were excluded for reporting extreme levels of heading. Generalized estimating equation linear regression models were employed to combine data across visits for a cross-sectional analysis of the data.
At each study visit every 3 to 6 months, players completed the HeadCount 12-Month Questionnaire, a validated, computer-based questionnaire to estimate 12-month heading exposure that was categorized as low (quartiles 1 and 2), moderate (quartile 3), and high (quartile 4).
Verbal memory was assessed at each study visit using the International Shopping List Delayed Recall task from CogState.
A total of 352 soccer players (256 men and 96 women; median age, 23 years [interquartile range, 21-28 years]) across a total of 1204 visits were analyzed. High levels of heading were associated with worse verbal memory performance (β = -0.59; 95% CI, -0.93 to -0.25; P = .001). There was no main association of APOE ε4 with verbal memory (β = 0.09; 95% CI, -0.24 to 0.42; P = .58). However, there was a significant association of APOE ε4 and heading with performance on the ISRL task (χ2 = 7.22; P = .03 for overall interaction). In APOE ε4-positive players, poorer verbal memory associated with high vs low heading exposure was 4.1-fold greater (APOE ε4 negative, β = -0.36; 95% CI, -0.75 to 0.03; APOE ε4 positive, β = -1.49; 95% CI, -2.05 to -0.93), and poorer verbal memory associated with high vs moderate heading exposure was 8.5-fold greater (APOE ε4 negative, β = -0.13; 95% CI, -0.54 to 0.29; APOE ε4 positive, β = -1.11, 95% CI, -1.70 to -0.53) compared with that in APOE ε4-negative players.
This study suggests that the APOE ε4 allele is a risk factor for worse memory performance associated with higher heading exposure in the prior year, which highlights that assessing genetic risks may ultimately play a role in promoting safer soccer play.
越来越多的证据表明,长期从事足球运动(世界上最受欢迎的运动)中的头球会增加认知障碍的风险。然而,载脂蛋白 E ε4(APOE ε4)等位基因(神经退行性疾病的常见风险因素)和头球与足球运动员认知之间的关联程度尚不清楚。
确定 APOE ε4 等位基因和 12 个月的头球暴露是否与成年业余足球运动员的言语记忆有关。
设计、地点和参与者:共有 379 名业余足球运动员于 2013 年 11 月 11 日至 2018 年 1 月 23 日参加了爱因斯坦足球研究的纵向研究。入选标准包括从事足球运动超过 5 年,每年超过 6 个月。在研究中登记的 379 人中,有 355 人进行了基因分型。有 3 名球员因报告极端的头球次数而被排除在外。使用广义估计方程线性回归模型对每次研究访问的数据进行组合,以对数据进行横截面分析。
在每次研究访问中(每 3 至 6 个月一次),球员使用 CogState 的国际购物清单延迟回忆任务评估 12 个月的头球暴露情况。该问卷是一种经过验证的基于计算机的问卷,用于估计 12 个月的头球暴露情况,分为低(第 1 四分位数和第 2 四分位数)、中(第 3 四分位数)和高(第 4 四分位数)暴露。
使用 CogState 的国际购物清单延迟回忆任务在每次研究访问中评估言语记忆。
在总共 1204 次访问中,共分析了 352 名足球运动员(256 名男性和 96 名女性;中位数年龄为 23 岁[四分位数间距 21-28 岁])。高水平的头球与言语记忆表现较差有关(β=-0.59;95%CI,-0.93 至-0.25;P=0.001)。APOE ε4 与言语记忆无主要关联(β=0.09;95%CI,-0.24 至 0.42;P=0.58)。然而,APOE ε4 和头球与 ISRL 任务的表现存在显著关联(χ2=7.22;P=0.03 用于整体交互作用)。在 APOE ε4 阳性的球员中,与低暴露相比,高水平的头球与较差的言语记忆之间的关联要强 4.1 倍(APOE ε4 阴性,β=-0.36;95%CI,-0.75 至 0.03;APOE ε4 阳性,β=-1.49;95%CI,-2.05 至-0.93),与低暴露相比,高水平的头球与较高暴露的言语记忆之间的关联要强 8.5 倍(APOE ε4 阴性,β=-0.13;95%CI,-0.54 至 0.29;APOE ε4 阳性,β=-1.11,95%CI,-1.70 至-0.53)。
这项研究表明,APOE ε4 等位基因是记忆表现较差的风险因素,与前一年较高的头球暴露有关,这突出表明评估遗传风险最终可能在促进更安全的足球运动中发挥作用。