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首页> 外文期刊>Journal of neurotrauma >Assessment of the macrophage marker quinolinic acid in cerebrospinal fluid after pediatric traumatic brain injury: insight into the timing and severity of injury in child abuse.
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Assessment of the macrophage marker quinolinic acid in cerebrospinal fluid after pediatric traumatic brain injury: insight into the timing and severity of injury in child abuse.

机译:小儿脑外伤后脑脊液中巨噬细胞标记喹啉酸的评估:了解虐待儿童的时间和严重程度。

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摘要

This study measured quinolinic acid (QUIN), a macrophage-microglia derived neurotoxin, in the cerebrospinal fluid (CSF) of children after non-inflicted and inflicted traumatic brain injury (nTBI, iTBI), and correlated QUIN concentrations with age, mechanism of injury (nTBi vs. iTBI), Glasgow Coma Scale (GCS) score and 6-month Glasgow Outcome Score. One hundred fifty-two CSF samples were collected from 51 children with severe TBI (GCS < or = 8). CSF was collected at the time an intraventricular catheter was placed and daily thereafter. QUIN concentration was measured by gas chromatography-mass spectroscopy. Patients ranged in age from 2 months to 16 years. Eleven children (22%) had iTBI. Initial and peak CSF QUIN concentrations were higher in patients with iTBI versus nTBI after adjusting for time after injury and GCS. Despite the lack of a history of trauma in 82% of children with iTBI, 100% had a peak QUIN concentration of >100 nM. There was a significant increase in the CSF concentrations of QUIN following severe nTBI and iTBI in children. Higher initial and peak QUIN concentrations after iTBI may be due to severity of injury, young age, and/or delay in seeking medical care, which allows for increased secondary injury.
机译:这项研究测量了未遭受和遭受外伤性脑损伤(nTBI,iTBI)后儿童脑脊髓液(CSF)中巨噬细胞-小胶质细胞衍生的神经毒素喹啉酸(QUIN),并将QUIN浓度与年龄,损伤机制相关联(nTBi与iTBI),格拉斯哥昏迷量表(GCS)得分和6个月的格拉斯哥成果得分。从51例重度TBI(GCS <或= 8)儿童中收集了125份CSF样本。放置脑室内导管时及其后每天收集CSF。通过气相色谱-质谱法测量QUIN浓度。患者的年龄从2个月到16岁不等。 11名儿童(22%)患有iTBI。调整伤后时间和GCS后,iTBI患者的初始和峰值CSF QUIN浓度高于nTBI患者。尽管在82%的iTBI儿童中没有创伤史,但100%的QUIN峰值浓度> 100 nM。严重的nTBI和iTBI患儿后,QUIN的CSF浓度显着增加。 iTBI后较高的初始和高峰QUIN浓度可能是由于损伤的严重程度,年龄和/或就医时间延迟所致,从而增加了继发性损伤。

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