Center for Neuroscience & Regenerative Medicine (CNRM), Uniformed Services University of the Health Sciences, Bethesda, Maryland, USA.
Department of Physical Medicine and Rehabilitation, School of Medicine, Virginia Commonwealth University, Richmond, Virginia, USA.
Brain Inj. 2022 Apr 16;36(5):633-643. doi: 10.1080/02699052.2022.2037711. Epub 2022 Feb 19.
Following mild traumatic brain injury (mTBI), many individuals suffer from persistent post-concussive, depressive, post-traumatic stress, and sleep-related symptoms. Findings from self-report scales link these symptoms to biomarkers of neurodegeneration, although the underlying pathophysiology is unclear. Each linked self-report scale includes sleep items, raising the possibility that despite varied symptomology, disordered sleep may underlie these associations. To isolate sleep effects, we examined associations between post-mTBI biomarkers of neurodegeneration and symptom scales according to composite, non-sleep, and sleep components.
Plasma biomarkers and self-report scales were obtained from 143 mTBI-positive warfighters. Pearson's correlations and regression models were constructed to estimate associations between total, sleep, and non-sleep scale items with biomarker levels, and with measured sleep quality.
Symptom severity positively correlated with biomarker levels across scales. Biomarker associations were largely unchanged when sleep items were included, excluded, or considered in isolation. Pittsburgh Sleep Quality Index demonstrated strong correlations with sleep and non-sleep items of all scales.
The congruency of associations raises the possibility of a common pathophysiological process underlying differing symptomologies. Given its role in neurodegeneration and mood dysregulation, sleep physiology seems a likely candidate. Future longitudinal studies should test this hypothesis, with a focus on identifying novel sleep-related therapeutic targets.
轻度创伤性脑损伤(mTBI)后,许多人会持续出现脑震荡后、抑郁、创伤后应激和睡眠相关症状。来自自我报告量表的研究结果将这些症状与神经退行性变的生物标志物联系起来,尽管潜在的病理生理学机制尚不清楚。每个相关的自我报告量表都包含睡眠项目,这表明尽管症状不同,但睡眠障碍可能是这些关联的基础。为了分离睡眠的影响,我们根据综合、非睡眠和睡眠成分,检查了 mTBI 后神经退行性变的生物标志物与症状量表之间的关联。
从 143 名 mTBI 阳性的战士中获得了血浆生物标志物和自我报告量表。构建 Pearson 相关系数和回归模型来估计总量表、睡眠量表和非睡眠量表项目与生物标志物水平以及测量的睡眠质量之间的关联。
症状严重程度与所有量表的生物标志物水平呈正相关。当包含、排除或单独考虑睡眠项目时,生物标志物的相关性变化不大。匹兹堡睡眠质量指数(PSQI)与所有量表的睡眠和非睡眠项目均有很强的相关性。
关联的一致性表明,不同症状可能存在共同的病理生理过程。鉴于睡眠生理学在神经退行性变和情绪失调中的作用,它似乎是一个很有前途的候选者。未来的纵向研究应检验这一假设,重点是确定新的与睡眠相关的治疗靶点。