Department of Pediatrics, Penn State College of Medicine, Pennsylvania State University, Hershey.
Department of Emergency Medicine, Penn State College of Medicine, Pennsylvania State University, Hershey.
JAMA Pediatr. 2018 Jan 1;172(1):65-73. doi: 10.1001/jamapediatrics.2017.3884.
Approximately one-third of children who experience a concussion develop prolonged concussion symptoms. To our knowledge, there are currently no objective or easily administered tests for predicting prolonged concussion symptoms. Several studies have identified alterations in epigenetic molecules known as microRNAs (miRNAs) following traumatic brain injury. No studies have examined whether miRNA expression can detect prolonged concussion symptoms.
To evaluate the efficacy of salivary miRNAs for identifying children with concussion who are at risk for prolonged symptoms.
DESIGN, SETTING, AND PARTICIPANTS: This prospective cohort study at the Penn State Medical Center observed 52 patients aged 7 to 21 years presenting for evaluation of concussion within 14 days of initial head injury, with follow-up at 4 and 8 weeks.
All patients had a clinical diagnosis of concussion.
Salivary miRNA expression was measured at the time of initial clinical presentation in all patients. Patients with a Sport Concussion Assessment Tool (SCAT3) symptom score of 5 or greater on self-report or parent report 4 weeks after injury were designated as having prolonged symptoms.
Of the 52 included participants, 22 (42%) were female, and the mean (SD) age was 14 (3) years. Participants were split into the prolonged symptom group (n = 30) and acute symptom group (n = 22). Concentrations of 15 salivary miRNAs spatially differentiated prolonged and acute symptom groups on partial least squares discriminant analysis and demonstrated functional relationships with neuronal regulatory pathways. Levels of 5 miRNAs (miR-320c-1, miR-133a-5p, miR-769-5p, let-7a-3p, and miR-1307-3p) accurately identified patients with prolonged symptoms on logistic regression (area under the curve, 0.856; 95% CI, 0.822-0.890). This accuracy exceeded accuracy of symptom burden on child (area under the curve, 0.649; 95% CI, 0.388-0.887) or parent (area under the curve, 0.562; 95% CI, 0.219-0.734) SCAT3 score. Levels of 3 miRNAs were associated with specific symptoms 4 weeks after injury; miR-320c-1 was associated with memory difficulty (R, 0.55; false detection rate, 0.02), miR-629 was associated with headaches (R, 0.47; false detection rate, 0.04), and let-7b-5p was associated with fatigue (R, 0.45; false detection rate, 0.04).
Salivary miRNA levels may identify the duration and character of concussion symptoms. This could reduce parental anxiety and improve care by providing a tool for concussion management. Further validation of this approach is needed.
大约三分之一经历脑震荡的儿童会出现长期的脑震荡症状。据我们所知,目前尚无用于预测长期脑震荡症状的客观或易于管理的测试方法。几项研究已经确定,在创伤性脑损伤后,几种称为 microRNAs (miRNAs) 的表观遗传分子会发生改变。尚无研究探讨 miRNA 表达是否可以检测到长期的脑震荡症状。
评估唾液 miRNA 识别有发生长期症状风险的脑震荡儿童的有效性。
设计、地点和参与者:这项前瞻性队列研究在宾夕法尼亚州立大学医学中心进行,观察了 52 名年龄在 7 至 21 岁之间的患者,他们在头部受伤后 14 天内出现脑震荡症状并接受评估,在 4 周和 8 周时进行随访。
所有患者均有临床脑震荡诊断。
所有患者在初始临床就诊时均测量唾液 miRNA 表达。自我报告或父母报告在受伤后 4 周时 SCAT3 症状评分≥5 分的患者被指定为有长期症状。
在纳入的 52 名参与者中,有 22 名(42%)为女性,平均(SD)年龄为 14(3)岁。参与者被分为长期症状组(n = 30)和急性症状组(n = 22)。部分最小二乘判别分析显示,15 种唾液 miRNA 的浓度可区分长期和急性症状组,并且表现出与神经元调节途径的功能关系。5 种 miRNA(miR-320c-1、miR-133a-5p、miR-769-5p、let-7a-3p 和 miR-1307-3p)的水平通过逻辑回归准确识别出长期症状患者(曲线下面积,0.856;95%CI,0.822-0.890)。这种准确性超过了儿童(曲线下面积,0.649;95%CI,0.388-0.887)或父母(曲线下面积,0.562;95%CI,0.219-0.734)SCAT3 评分的症状负担准确性。3 种 miRNA 的水平与受伤后 4 周的特定症状相关;miR-320c-1 与记忆困难相关(R,0.55;假阳性率,0.02),miR-629 与头痛相关(R,0.47;假阳性率,0.04),let-7b-5p 与疲劳相关(R,0.45;假阳性率,0.04)。
唾液 miRNA 水平可能可以识别脑震荡症状的持续时间和特征。这可以通过提供一种用于脑震荡管理的工具来减轻父母的焦虑并改善护理。需要进一步验证这种方法。