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The effect of serum malondialdehyde on the short-term prognosis of the patients with severe traumatic brain injury in the plateau |
Li Wen-hui, Ju Hu |
Department of Neurosurgery, Qinghai University Affiliated Hospital, Xining 810001, China |
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Abstract Objective To evaluate the relationship between serum malondialdehyde (MDA) and the short-term prognosis in patients with severe traumatic brain injury (sTBI) in the plateau. Methods A total of 98 patients with sTBI treated by neurosurgery in our hospital were selected as a study group (the sTBI group, n=98). 100 healthy people who took physical examination in our hospital during the same period were selected as a control group (the control group, n=100). At the ICU treatment on the 1st, 3rd, 7th and 15th day, the sTBI patients were drawn 5 mL venous blood, and the patient′s MDA concentration was measured. 6 months after admission, the prognosis was evaluated according to the Glasgow Outcome Scale (GOS). The patients with sTBI were divided into the good prognosis group and the poor prognosis group. The difference of MDA between the sTBI group and the control group and the change of MDA in patients during ICU treatment were evaluated. The MDA value of the good prognosis group, the poor prognosis group and the control group were compared. Univariate and multivariate analysis were used to evaluate the factors affecting the poor prognosis of patients. The accuracy of the MDA value for predicting poor prognosis has been evaluated. The patients were divided into high MDA group and low MDA group according to the cut-off value when the Youden index was the maximum. The cumulative survival rate of patients with high MDA and low MDA was compared. Results Of the 98 patients in the sTBI group, 52 (53.1%) had a poor prognosis and 46 (46.9%) patients had a good prognosis. The patients with poor prognosis and good prognosis had significantly higher MDA values than those in the control group (all P<0.001). The patients with poor prognosis had significantly higher MDA values than those with good prognosis (P<0.001). On the 3rd, 7th and 15th days, the MDA value of the patients with poor prognosis group was significantly higher than that of the good prognosis group, with statistical significance (all P<0.001). The multivariate logistic regression model showed that serum MDA increased the 6-month poor prognosis of patients with sTBI[OR=4.662, 95%CI1.466~14.824, P=0.018]. The MDA in patients with sTBI (AUC=0.763, sensitivity=52%, specificity=85%, Youden index=0.37, cut-off value 2.963 nmol/mL) was highly accurate in predicting poor prognosis. The cumulative survival rate of patients with high MDA (MDA>2.963 nmol/mL) was significantly lower than that of patients with low MDA (HR=3.615, 95%CI1.429~8.481, P<0.001). Conclusion ROS-mediated oxidative damage plays an important role in the prognosis of sTBI in plateau. High MDA in patients with sTBI increase the risk of poor prognosis in patients.
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[1]Varghese R, Chakrabarty J, Menon G. Nursing Management of Adults with Severe Traumatic Brain Injury: A Narrative Review[J]. Indian J Crit Care Med, 2017, 21(10):684-697.
[2]张红艳,柳璐. 重型颅脑损伤后SIRS、sepsis、严重sepsis和MODS发生机制的研究进展[J]. 广东医学, 2012, 33(9): 1335-1337.
[3]周龙,郁毅刚. 重型颅脑损伤后的失神经调节-免疫紊乱机制[J]. 中华神经医学杂志, 2013, 12(11): 1186-1188.
[4]Halstrom A, MacDonald E, Neil C, et al. Elevation of oxidative stress indicators in a pilot study of plasma following traumatic brain injury[J]. J Clin Neurosci, 2017, 35:104-108.
[5]Nayak C, Nayak D, Bhat S, et al. Relationship between neurological outcome and early oxidative changes in erythrocytes in head injury patients[J]. Clin Chem Lab Med, 2007, 45(5):629-633.
[6]Hohl A, Gullo Jda S, Silva CC, et al. Plasma levels of oxidative stress biomarkers and hospital mortality in severe head injury: a multivariate analysis[J]. J Crit Care, 2012, 27(5):523.e11-9.〖JP〗
[7]曹成龙,李艳玲,宋健,等. 急性中、重型颅脑损伤早期病死率的预测:Marshall CT分级和Rotterdam CT评分的比较[J]. 中国临床神经外科杂志, 2017, 22(10): 676-679.
[8]白玉婷,周白丽,谭茗月,等. 高原地区原发性高血压患者SOD、MDA含量变化研究[J]. 西部医学, 2012, 24(3): 465-467.
[9]Lorente L. New Prognostic Biomarkers in Patients With Traumatic Brain Injury[J]. Arch Trauma Res, 2015, 4(4):e30165.
[10]胡学安,胡世颉,李兵,等. 亚低温脑保护在创伤性颅脑损伤治疗中的应用效果分析[J]. 陕西医学杂志, 2014, 43(4): 398-400. [11]王琰,李洁,郑洪佳. 高压氧治疗在重型颅脑损伤的临床效果及多方机制综合分析[J]. 脑与神经疾病杂志, 2016, 24(7): 439-442.
[12]Hall ED, Vaishnav RA, Mustafa AG. Antioxidant therapies for traumatic brain injury[J]. Neurotherapeutics, 2010, 7(1):51-61.
[13]黄云柯,黄熙. 脑外伤急性氧化损伤时间过程:问题与对策[J]. 中南大学学报(医学版), 2014, 39(2): 195-198.
[14]吴志宝,孙国柱,孙博宇,等. 氧化应激在大鼠液压冲击性脑损伤中的时程变化和意义[J]. 脑与神经疾病杂志, 2016, 24(12): 727-730.
[15]Saniova B, Drobny M, Lehotsky J, et al. Biochemical and clinical improvement of cytotoxic state by amantadine sulphate[J]. Cell Mol Neurobiol, 2006, 26(7-8):1475-1482. |
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