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首页> 外文期刊>Neurologia medico-chirurgica. >Probability of Soluble Tissue Factor Release Lead to the Elevation of D-dimer as a Biomarker for Traumatic Brain Injury
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Probability of Soluble Tissue Factor Release Lead to the Elevation of D-dimer as a Biomarker for Traumatic Brain Injury

机译:可溶性组织因子释放的概率导致D-二聚体的升高作为创伤性脑损伤的生物标志物

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D-dimer is a potential biomarker for the detection of traumatic brain injury (TBI). However, the mechanisms that trigger elevation of D-dimer in TBI remain unclear. The purpose of this study was to evaluate the reliability of D-dimer in blood as a biomarker for TBI and to determine the mechanisms involved in regulating its blood levels. Nine patients with moderate to severe isolated TBI (Glasgow Coma Scale [GCS] score 7-13) were admitted to our hospital from May 2013 to June 2014. Blood samples were collected from systemic arteries on arrival and at 1, 3, 5, and 7 days after injury. Blood levels of neuron specific enolase (NSE), D-dimer, and soluble tissue factor (sTF) were measured. NSE (33.4 ng/ml: normal 12.0 ng/ml) and D-dimer (56.1 mu g/ml: normal 1.0 mu g/ml) were elevated at admission and declined on day 1 after injury. At admission, there were significant correlations of D-dimer levels with NSE (R = 0.727, P = 0.026) and sTF (R = 0.803, P = 0.009) levels. The blood level of D-dimer accurately reflects the degree of brain tissue damage indicated by NSE levels. Our data suggest that release of sTF induced by brain tissue damage may activate the coagulation cascade, leading to elevation of D-dimer.
机译:D-二聚体是用于检测创伤性脑损伤(TBI)的潜在生物标志物。然而,在TBI中触发D-二聚体升高的机制仍不清楚。本研究的目的是评估血液中D-二聚体作为TBI的生物标志物的可靠性,并确定调节其血液水平的机制。九月至2013年5月至2014年6月入院,九至2014年6月入院,九月至2014年6月,九月至2014年6月入院。从2013年5月到2014年6月,从2014年5月入院,九升患者。受伤后7天。测量神经元特异性烯醇酶(NSE),D-二聚体和可溶性组织因子(STF)的血液水平。 NSE(33.4ng / mL:正常& 12.0ng / ml)和D-二聚体(56.1μg/ ml:正常的12.0μmg/ ml)在入院时升高,损伤后第1天下降。在入院时,D-二聚体水平与NSE(r = 0.727,p = 0.026)和STF(r = 0.803,p = 0.009)水平具有显着的相关性。 D-二聚体的血液水平精确地反映了NSE水平所示的脑组织损伤程度。我们的数据表明,脑组织损伤诱导的STF释放可能激活凝固级联,导致D-二聚体的升高。

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