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首页> 外文期刊>Forensic science international >Concentration of microtubule associated protein tau (MAPT) in urine and saliva as a potential biomarker of traumatic brain injury in relationship with blood-brain barrier disruption in postmortem examination
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Concentration of microtubule associated protein tau (MAPT) in urine and saliva as a potential biomarker of traumatic brain injury in relationship with blood-brain barrier disruption in postmortem examination

机译:尿液和唾液中微管相关蛋白Tau(MAPT)的浓度作为血脑屏障碍中血脑屏屏障的创伤性脑损伤的潜在生物标志物

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Traumatic brain injury (TBI) constitutes a frequent finding in medico-legal practice, including forensic autopsy and neuropathological examination. Despite clinico-scientific advances there is a need for identification of novel biomarkers considered for TBI diagnostics in ante- and postmortem cases. The role of MAPT protein as a biomarker in case of TBI was investigated in previous studies by examination of blood and cerebrospinal fluid obtained during forensic autopsies whereas less is known concerning its liberation and occurrence in other biofluids. The aim of this study was to elucidate and identify if elevated MAPT levels in other biofluids, such as urine, saliva, and vitreous body are also seen in TBI cases in population-based autopsy screening. The study was carried out using cases (n = 14) of severe head injury suspected as the cause of death and control cases (n= 13) of sudden death in the mechanism of cardiopulmonary failure. The biofluids, such as urine, saliva, and vitreous body were collected within similar to 24 h after death and compared using ELISA test. Tissue specimens including brain and kidney were similarly collected during forensic autopsies. Brain specimens were stained immunohistologically with anti-Vimentin (V9) antibody and histologically using Mallory's trichrome method (to assess structural damage to blood-brain barrier elements) whereas kidney specimens were stained immunohistologically with anti-MAPT antibody (to assess the suitability of such a study in the diagnosis of TBI). In our study, we observed the elevated concentration levels of MAPT in saliva and urine. These changes were accompanied by damage to the structural elements of the blood-brain barrier (damage to the vascular endothelium and vascular basement membrane). According to this elevated cencentration levels of MAPT in this biofluids should be considered as TBI marker in postmortem examination even in cases where the head injury was not supposed to consist the direct cause of death. (C) 2019 Elsevier B.V. All rights reserved.
机译:创伤性脑损伤(TBI)构成Medico-法律实践的频繁发现,包括法医尸检和神经病理学检查。尽管临床科学进步,但需要鉴定考虑在患者和后期案件中考虑TBI诊断的新型生物标志物。在先前的研究中研究了MAPT蛋白作为生物标志物的作用,通过检查在法医尸检期间获得的血液和脑脊液,而较少是较低的关于其释放和在其他生物流体中的发生。本研究的目的是阐明和鉴定其他生物流体的MAPT水平,如尿液,唾液和玻璃体等尿液,唾液和玻璃体,在基于群体的尸检筛查中也可以看到。使用患者(n = 14)进行严重头部损伤的病例(n = 14),作为心肺功能衰竭机制猝死的死亡和对照病例(n = 13)。在死亡后24小时内收集生物流体,例如尿液,唾液和玻璃体,并使用ELISA试验比较。在法医尸检期间类似地收集包括脑和肾的组织标本。用抗Vimentin(V9)抗体(V9)抗体染色脑标本,并使用Mallory的血管系法组织学(以评估对血脑屏障元件的结构损伤),而肾脏标本用抗Mapt抗体染色免疫组织学(以评估该a的适用性) TBI诊断的研究)。在我们的研究中,我们观察到唾液和尿液中MAPT的浓度升高。这些变化伴随着血脑屏障的结构元素的损害(血管内皮和血管基底膜损伤)。根据这种生物流体中MAPT的脑膜脑水平,即使在颅脑损伤不包括直接死因的情况下,这种生物流体中的MAPT患者应被视为TBI标志物。 (c)2019年Elsevier B.V.保留所有权利。

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