Linnstaedt Sarah D, Zannas Anthony S, McLean Samuel A, Koenen Karestan C, Ressler Kerry J
Institute for Trauma Recovery, University of North Carolina, Chapel Hill, NC, USA.
Department of Anesthesiology, University of North Carolina, Chapel Hill, NC, USA.
Mol Psychiatry. 2020 Sep;25(9):1986-1999. doi: 10.1038/s41380-019-0636-5. Epub 2019 Dec 20.
Exposure to traumatic events is common. While many individuals recover following trauma exposure, a substantial subset develop adverse posttraumatic neuropsychiatric sequelae (APNS) such as posttraumatic stress, major depression, and regional or widespread chronic musculoskeletal pain. APNS cause substantial burden to the individual and to society, causing functional impairment and physical disability, risk for suicide, lost workdays, and increased health care costs. Contemporary treatment is limited by an inability to identify individuals at high risk of APNS in the immediate aftermath of trauma, and an inability to identify optimal treatments for individual patients. Our purpose is to provide a comprehensive review describing candidate blood-based biomarkers that may help to identify those at high risk of APNS and/or guide individual intervention decision-making. Such blood-based biomarkers include circulating biological factors such as hormones, proteins, immune molecules, neuropeptides, neurotransmitters, mRNA, and noncoding RNA expression signatures, while we do not review genetic and epigenetic biomarkers due to other recent reviews of this topic. The current state of the literature on circulating risk biomarkers of APNS is summarized, and key considerations and challenges for their discovery and translation are discussed. We also describe the AURORA study, a specific example of current scientific efforts to identify such circulating risk biomarkers and the largest study to date focused on identifying risk and prognostic factors in the aftermath of trauma exposure.
遭受创伤性事件很常见。虽然许多人在经历创伤后能够恢复,但仍有相当一部分人会出现创伤后神经精神后遗症(APNS),如创伤后应激障碍、重度抑郁症以及局部或全身性慢性肌肉骨骼疼痛。APNS给个人和社会带来了沉重负担,导致功能障碍和身体残疾、自杀风险、工作日损失以及医疗费用增加。当代治疗方法存在局限性,无法在创伤后立即识别出有APNS高风险的个体,也无法为个体患者确定最佳治疗方案。我们的目的是提供一篇全面综述,描述基于血液的候选生物标志物,这些标志物可能有助于识别有APNS高风险的个体和/或指导个体干预决策。此类基于血液的生物标志物包括循环生物因子,如激素、蛋白质、免疫分子、神经肽、神经递质、mRNA和非编码RNA表达特征,不过由于近期已有关于该主题的其他综述,我们不涉及遗传和表观遗传生物标志物。本文总结了APNS循环风险生物标志物的文献现状,并讨论了其发现和转化过程中的关键考虑因素及挑战。我们还介绍了AURORA研究,这是当前识别此类循环风险生物标志物的科学努力的一个具体例子,也是迄今为止专注于识别创伤暴露后风险和预后因素的最大规模研究。