脑震荡后 28 天症状患者受伤当天的微纳生物标志物:前瞻性队列研究

Biswadev Mitra, Brendan Major, Jonathan Reyes, Nanda Surendran, Jesse Bain, Lauren P Giesler, William T O'Brien, Edmond Sorich, Catherine Willmott, Sandy R Shultz, Terence J O'Brien, Jeffrey V Rosenfeld, Stuart J McDonald
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引用次数: 0

摘要

背景:轻度创伤性脑损伤(mTBI)后,一些患者会出现持续数周至数月的症状。轻微创伤性脑损伤后的恢复情况主要通过自述症状问卷进行评估。血液生物标志物,包括微RNA种类,已显示出协助诊断mTBI的前景,然而,人们对血液微RNA测量如何预测症状恢复知之甚少:本研究旨在调查在受伤 28 天时报告出现脑震荡后症状的 mTBI 患者与未报告出现脑震荡后症状的患者之间在受伤当天血浆 microRNA 的差异:方法: 对受伤当天到成人三级转诊医院急诊科就诊并被诊断为孤立性 mTBI 的患者(n=35)进行为期 28 天的随访。采集静脉血液样本,并在受伤当天和28天后使用Rivermead脑震荡后症状问卷(RPQ)评估症状严重程度。将 RPQ 总分≥10 分或至少一种症状严重程度≥2 分的持续症状患者与症状严重程度较轻或症状缓解的患者进行比较:有 9 名患者(25.7%;95%CI:12.5-43.3)报告了持续症状。与没有持续症状的患者相比,受伤当天血浆 miR-223-3p 水平明显较高,但 miRs 142-3p、423-3p、32-5p、144-3p 和 let-7f-5p 没有观察到这种差异:结论:急性血浆 miR-223-3p 水平似乎能检测出 mTBI 后出现持续症状的患者。结论:急性血浆 miR-223-3p 水平似乎能检测出 mTBI 后出现持续症状的患者,这些结果表明,此类生物标志物具有潜在的实用性,可帮助做出早期转诊治疗的决定。
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MicroRNA Biomarkers on Day of Injury Among Patients with Post Concussive Symptoms at 28-Days: A Prospective Cohort Study.

Background: After mild traumatic brain injury (mTBI), some patients experience symptoms that persist for weeks to months. Recovery from mTBI is primarily assessed using selfreported symptom questionnaires. Blood biomarkers, including microRNA species, have shown promise to assist diagnosis of mTBI, however, little is known about how blood microRNA measures might predict symptom recovery.

Objective: The aim of this study was to investigate the variances in plasma microRNAs on the day of injury between individuals with mTBI who report post-concussive symptoms at the 28- day mark and those who do not.

Methods: Patients who presented to an adult, tertiary referral hospital emergency department on the day of the injury and were diagnosed with isolated mTBI (n=35) were followed up for 28 days. Venous blood samples were collected and symptom severity was assessed using the Rivermead Post-Concussion Symptom Questionnaire (RPQ) on the day of injury and at 28 days. Patients who reported ongoing symptoms of total RPQ score ≥10 or at least one symptom severity ≥2, were compared to those with lesser symptom severity or symptom resolution.

Results: There were 9 (25.7%; 95%CI: 12.5-43.3) patients who reported persistent symptoms. Day of injury plasma miR-223-3p levels were significantly higher in individuals with ongoing symptoms compared to those without, however, no such differences were observed for miRs 142- 3p, 423-3p, 32-5p, 144-3p, and let-7f-5p.

Conclusion: Acute plasma miR-223-3p levels appear to detect patients who later have persistent symptoms after mTBI. The results demonstrate the potential utility for such biomarkers to assist in decisions towards early referral for therapy after mTBI.

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