Quadrant Biosciences, Syracuse, NY, 13210, USA.
Department of Family Medicine, Penn State College of Medicine, Hershey, PA, 17033, USA.
J Neurol. 2021 Nov;268(11):4349-4361. doi: 10.1007/s00415-021-10566-x. Epub 2021 May 24.
The goals of this study were to assess the ability of salivary non-coding RNA (ncRNA) levels to predict post-concussion symptoms lasting ≥ 21 days, and to examine the ability of ncRNAs to identify recovery compared to cognition and balance.
RNA sequencing was performed on 505 saliva samples obtained longitudinally from 112 individuals (8-24-years-old) with mild traumatic brain injury (mTBI). Initial samples were obtained ≤ 14 days post-injury, and follow-up samples were obtained ≥ 21 days post-injury. Computerized balance and cognitive test performance were assessed at initial and follow-up time-points. Machine learning was used to define: (1) a model employing initial ncRNA levels to predict persistent post-concussion symptoms (PPCS) ≥ 21 days post-injury; and (2) a model employing follow-up ncRNA levels to identify symptom recovery. Performance of the models was compared against a validated clinical prediction rule, and balance/cognitive test performance, respectively.
An algorithm using age and 16 ncRNAs predicted PPCS with greater accuracy than the validated clinical tool and demonstrated additive combined utility (area under the curve (AUC) 0.86; 95% CI 0.84-0.88). Initial balance and cognitive test performance did not differ between PPCS and non-PPCS groups (p > 0.05). Follow-up balance and cognitive test performance identified symptom recovery with similar accuracy to a model using 11 ncRNAs and age. A combined model (ncRNAs, balance, cognition) most accurately identified recovery (AUC 0.86; 95% CI 0.83-0.89).
ncRNA biomarkers show promise for tracking recovery from mTBI, and for predicting who will have prolonged symptoms. They could provide accurate expectations for recovery, stratify need for intervention, and guide safe return-to-activities.
本研究旨在评估唾液非编码 RNA(ncRNA)水平预测脑震荡后持续时间超过 21 天的症状的能力,并检验 ncRNA 识别恢复情况的能力与认知和平衡能力相比。
对 112 例轻度创伤性脑损伤(mTBI)患者的 505 份唾液样本进行 RNA 测序。初始样本采集于损伤后≤14 天,随访样本采集于损伤后≥21 天。在初始和随访时间点评估计算机平衡和认知测试表现。使用机器学习来定义:(1)一种使用初始 ncRNA 水平预测损伤后持续时间超过 21 天的持续性脑震荡后症状(PPCS)的模型;(2)一种使用随访 ncRNA 水平来识别症状恢复的模型。分别将模型的性能与经过验证的临床预测规则和平衡/认知测试表现进行比较。
使用年龄和 16 个 ncRNA 的算法预测 PPCS 的准确性优于经过验证的临床工具,且具有附加的综合效用(曲线下面积(AUC)0.86;95%置信区间(CI)0.84-0.88)。PPCS 和非 PPCS 组之间的初始平衡和认知测试表现没有差异(p>0.05)。随访平衡和认知测试表现与使用 11 个 ncRNA 和年龄的模型识别症状恢复的准确性相似。ncRNA、平衡和认知的综合模型最准确地识别恢复(AUC 0.86;95%CI 0.83-0.89)。
ncRNA 生物标志物有望用于跟踪 mTBI 的恢复,并预测哪些患者会出现持续症状。它们可以提供准确的恢复预期,分层干预需求,并指导安全恢复活动。