Department of Kinesiology, Temple University, Philadelphia, Pennsylvania, USA.
Clin J Sport Med. 2010 Nov;20(6):464-8. doi: 10.1097/JSM.0b013e3181fc0a81.
To evaluate the association between apolipoprotein E (APOE) polymorphisms (E2, C/T Arg158Cys; E4, T/C Cys112Arg; and promoter, g-219t) and the history of concussion in college athletes. We hypothesized that carrying 1 or more APOE rare (or minor) allele assessed in this study would be associated with having a history of 1 or more concussions.
Multicenter cross-sectional study.
University athletic facilities.
One hundred ninety-six male football (n = 163) and female soccer (n = 33) college athletes volunteered.
Written concussion history questionnaire and saliva samples for genotyping.
Self-reported history of a documented concussion and rare APOE genotype (E2, E4, promoter).
There was a significant association (Wald χ² = 3.82; P = 0.05; odds ratio = 9.8) between carrying all APOE rare alleles and the history of a previous concussion. There was also a significant association (Wald χ² = 3.96, P = 0.04, odds ratio = 8.4) between carrying the APOE promoter minor allele and experiencing 2 or more concussions.
Carriers of all 3 APOE rare (or minor) alleles assessed in this study were nearly 10 times more likely to report a previous concussion and may be at a greater risk of concussion versus noncarriers. Promoter minor allele carriers were 8.4 times more likely to report multiple concussions and may be at a greater risk of multiple concussions versus noncarriers. Research involving larger samples of individuals with multiple concussions and carriers of multiple APOE rare alleles is warranted.
评估载脂蛋白 E(APOE)多态性(E2、C/T Arg158Cys;E4、T/C Cys112Arg;以及启动子,g-219t)与大学生运动员脑震荡史之间的关系。我们假设,在本研究中评估的携带 1 个或更多 APOE 罕见(或次要)等位基因与有 1 个或更多脑震荡史有关。
多中心横断面研究。
大学体育设施。
196 名男性足球运动员(n=163)和女性足球运动员(n=33)自愿参加。
书面脑震荡史问卷和用于基因分型的唾液样本。
自我报告的有记录的脑震荡史和罕见的 APOE 基因型(E2、E4、启动子)。
携带所有 APOE 罕见等位基因与既往脑震荡史之间存在显著关联(Wald χ²=3.82;P=0.05;优势比=9.8)。携带 APOE 启动子次要等位基因与经历 2 次或更多脑震荡之间也存在显著关联(Wald χ²=3.96,P=0.04,优势比=8.4)。
在本研究中评估的所有 3 种 APOE 罕见(或次要)等位基因的携带者报告既往脑震荡的可能性几乎增加了 10 倍,与非携带者相比,他们可能更容易发生脑震荡。启动子次要等位基因携带者报告多次脑震荡的可能性增加了 8.4 倍,与非携带者相比,他们可能更容易发生多次脑震荡。需要对有多次脑震荡史和携带多个 APOE 罕见等位基因的个体进行更大样本的研究。