Albert Venencia, Subramanian Arulselvi, Agrawal Deepak, Bhoi Sanjeev Kumar, Pallavi Pooja, Mukhopadhayay A K
Departments of Laboratory Medicine, Jai Prakash Narayan Apex Trauma Center, AIIMS, New Delhi, 110022, India.
Department of Neurosurgery, Jai Prakash Narayan Apex Trauma Center, AIIMS, New Delhi, 110022, India.
BMC Res Notes. 2017 Mar 24;10(1):139. doi: 10.1186/s13104-017-2459-2.
Traumatic brain injury (TBI) causes activation of several neurochemical and physiological cascades, leading to neurological impairment. We aimed to investigate the level of novel chemokine RANTES in plasma, cerebrospinal fluid (CSF) and contused brain tissue in traumatic brain injury patients and to correlate the expression of this chemokine with the severity of head injury and neurological outcome.
This longitudinal case control study was performed on 70 TBI patients over a period of 30 months. Glasgow coma scale (GCS) and Glasgow outcome score were used to assess the severity of head injury and clinical outcome. Level of RANTES was quantified in plasma (n = 60), CSF (N = 10) and contused brain tissue (n = 5). Alterations in the plasma levels on 1st and 5th day following TBI were assessed. Patients were categorized as severe (GCS < 8) (SHI), moderate and mild Head injury (GCS > 8-14). 15 healthy volunteers were taken as the control group.
The median plasma RANTES levels were 971.3 (88.40-1931.1); 999.2 (31.2-2054.9); 471.8 (370.9-631.9) for SHI, MHI and healthy control respectively and showed statistically significant variation (p = 0.005). There was no statistical difference in the mean 1st and 5th day RANTES levels for the SHI group. However, admission RANTES levels were significantly higher in patients who died than those who survived (p = 0.04). Also, RANTES levels were significantly higher in plasma as compared to contused brain tissue and CSF (p = 0.0001).
This is the first study of its kind which shows that there is significant correlation of admission RANTES levels and early mortality. Another interesting finding was the significant upregulated in the expression of RANTES in plasma, compared to CSF and contused brain tissue following severe TBI.
创伤性脑损伤(TBI)会引发多种神经化学和生理级联反应,导致神经功能障碍。我们旨在研究创伤性脑损伤患者血浆、脑脊液(CSF)和挫伤脑组织中新型趋化因子调节激活正常T细胞表达和分泌的趋化因子(RANTES)的水平,并将这种趋化因子的表达与头部损伤的严重程度和神经学结果相关联。
这项纵向病例对照研究在70例TBI患者中进行,为期30个月。采用格拉斯哥昏迷量表(GCS)和格拉斯哥预后评分来评估头部损伤的严重程度和临床结果。对血浆(n = 60)、脑脊液(n = 10)和挫伤脑组织(n = 5)中的RANTES水平进行定量分析。评估TBI后第1天和第5天血浆水平的变化。患者被分为重度(GCS < 8)(SHI)、中度和轻度头部损伤(GCS > 8 - 14)。选取15名健康志愿者作为对照组。
SHI组、MHI组和健康对照组的血浆RANTES水平中位数分别为971.3(88.40 - 1931.1);999.2(31.2 - 2054.9);471.8(370.9 - 631.9),差异具有统计学意义(p = 0.005)。SHI组第1天和第5天的RANTES平均水平无统计学差异。然而,死亡患者的入院RANTES水平显著高于存活患者(p = 0.04)。此外,血浆中的RANTES水平显著高于挫伤脑组织和脑脊液(p = 0.0001)。
这是同类研究中的首个研究,表明入院RANTES水平与早期死亡率存在显著相关性。另一个有趣的发现是,与重度TBI后的脑脊液和挫伤脑组织相比,血浆中RANTES的表达显著上调。