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本文引用的文献

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Higher exosomal tau, amyloid-beta 42 and IL-10 are associated with mild TBIs and chronic symptoms in military personnel.较高的外泌体tau蛋白、β淀粉样蛋白42和白细胞介素-10与军事人员的轻度创伤性脑损伤及慢性症状相关。
Brain Inj. 2018;32(10):1277-1284. doi: 10.1080/02699052.2018.1471738. Epub 2018 Jun 18.
2
Association of Mild Traumatic Brain Injury With and Without Loss of Consciousness With Dementia in US Military Veterans.轻度创伤性脑损伤与非意识丧失性轻度创伤性脑损伤与美国退伍军人痴呆的关联。
JAMA Neurol. 2018 Sep 1;75(9):1055-1061. doi: 10.1001/jamaneurol.2018.0815.
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Functional Neuroanatomy of Emotion and Its Regulation in PTSD.创伤后应激障碍的情绪功能神经解剖及其调控
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Posttraumatic Stress Disorder and Depression Symptom Severities Are Differentially Associated With Hippocampal Subfield Volume Loss in Combat Veterans.创伤后应激障碍和抑郁症状的严重程度与退伍军人海马亚区体积减少存在不同程度的关联。
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Elevated tau and interleukin-6 concentrations in adults with obstructive sleep apnea.阻塞性睡眠呼吸暂停患者的 tau 蛋白和白细胞介素-6 浓度升高。
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Traumatic brain injury and the risk of dementia diagnosis: A nationwide cohort study.创伤性脑损伤与痴呆诊断风险:一项全国性队列研究。
PLoS Med. 2018 Jan 30;15(1):e1002496. doi: 10.1371/journal.pmed.1002496. eCollection 2018 Jan.
7
Traumatic brain injury may not increase the risk of Alzheimer disease.创伤性脑损伤可能不会增加患阿尔茨海默病的风险。
Neurology. 2017 Oct 31;89(18):1923-1925. doi: 10.1212/WNL.0000000000004608. Epub 2017 Oct 4.
8
Inflammation Relates to Chronic Behavioral and Neurological Symptoms in Military Personnel with Traumatic Brain Injuries.炎症与创伤性脑损伤军人的慢性行为和神经症状有关。
Cell Transplant. 2017 Jul;26(7):1169-1177. doi: 10.1177/0963689717714098.
9
Slow wave sleep disruption increases cerebrospinal fluid amyloid-β levels.慢波睡眠中断会增加脑脊液中β淀粉样蛋白的水平。
Brain. 2017 Aug 1;140(8):2104-2111. doi: 10.1093/brain/awx148.
10
Post-traumatic stress disorder and risk of dementia among members of a health care delivery system.创伤后应激障碍与医疗保健系统成员的痴呆风险。
Alzheimers Dement. 2018 Jan;14(1):28-34. doi: 10.1016/j.jalz.2017.04.014. Epub 2017 Jun 13.

同时患有轻度创伤性脑损伤和创伤后应激障碍与外周血血浆中 Tau 浓度升高有关。

Concurrent Mild Traumatic Brain Injury and Posttraumatic Stress Disorder Is Associated With Elevated Tau Concentrations in Peripheral Blood Plasma.

机构信息

National Institutes of Health, National Institute of Nursing Research, Bethesda, Maryland, USA.

Defense and Veterans Brain Injury Center, Walter Reed National Military Medical Center, Bethesda, Maryland, USA.

出版信息

J Trauma Stress. 2019 Aug;32(4):546-554. doi: 10.1002/jts.22418. Epub 2019 Jul 10.

DOI:10.1002/jts.22418
PMID:31291489
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6690750/
Abstract

Concurrent mild traumatic brain injury (mTBI) and posttraumatic stress disorder (PTSD) are common in U.S. military service members and veterans. Tau and amyloid-beta-42 (Aβ42) are proteins that have been linked to cognitive impairment, neurological hallmarks of Alzheimer's disease, and may also relate to recovery from mTBI. However, the role of these proteins in the maintenance or resolution of chronic symptoms has not yet been determined. Participants in the current study were 102 service members and veterans who had sustained an mTBI (n = 84) or injured controls (IC) without TBI (n = 18). They were categorized into three groups based on the presence or absence of mTBI and PTSD: IC/PTSD-Absent (n = 18), mTBI/PTSD-Absent (n = 63), and mTBI/PTSD-Present (n = 21). Concentrations of tau and Aβ42 in peripheral blood plasma were measured using Simoa , an ultrasensitive technology, and compared across groups. Tau concentrations were highest in the mTBI/PTSD-Present group, F(2, 99) = 4.33, p = .016, compared to the other two groups. Linear multiple regression was conducted to determine the independent effects of PTSD and mTBI on tau concentrations, controlling for gender and sleep medication. PTSD was a significant and independent predictor of tau concentrations, β = .25, p = .009, η = .26. Aβ42 concentrations did not differ between the groups. The results indicated that PTSD was associated with an elevation of tau in peripheral blood and suggest that there may be increased biological effects of PTSD in this young cohort of service members and veterans following mTBI.

摘要

同时患有轻度创伤性脑损伤(mTBI)和创伤后应激障碍(PTSD)在美国军人和退伍军人中很常见。tau 和淀粉样蛋白-β-42(Aβ42)是与认知障碍、阿尔茨海默病的神经标志有关的蛋白质,也可能与 mTBI 的恢复有关。然而,这些蛋白质在维持或解决慢性症状中的作用尚未确定。本研究的参与者是 102 名患有 mTBI(n = 84)或无创伤性脑损伤的受伤对照组(IC)的军人和退伍军人(n = 18)。他们根据是否存在 mTBI 和 PTSD 分为三组:IC/PTSD-无(n = 18)、mTBI/PTSD-无(n = 63)和 mTBI/PTSD-有(n = 21)。使用 Simoa 技术测量外周血血浆中 tau 和 Aβ42 的浓度,并在各组之间进行比较。tau 浓度在 mTBI/PTSD-有组中最高,F(2, 99) = 4.33, p =.016,与其他两组相比。进行线性多元回归以确定 PTSD 和 mTBI 对 tau 浓度的独立影响,同时控制性别和睡眠药物。PTSD 是 tau 浓度的显著独立预测因子,β =.25, p =.009,η =.26。各组之间 Aβ42 浓度无差异。结果表明,PTSD 与外周血中 tau 的升高有关,这表明在这群年轻的军人和退伍军人中,mTBI 后 PTSD 可能具有更大的生物学影响。