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作 者:杨阳[1] 范玉琛[1] 赵泽华[1] 纪相芬 窦橙云[1] 张建军[1] 王凯[1]
机构地区:[1]山东大学齐鲁医院肝病科,山东大学肝病研究所,济南250012
出 处:《中华实验和临床病毒学杂志》2014年第2期102-104,共3页Chinese Journal of Experimental and Clinical Virology
摘 要:目的检测慢加急性肝衰竭患者外周血单个核细胞(PBMC)中硫氧还蛋白-1(Trx-1)、硫氧还蛋白-2(Trx.2)mRNA水平并探讨其临床意义。方法收集60例慢加急性肝衰竭患者(肝衰竭组),38例慢性乙型肝炎患者(慢性乙型肝炎组),26例健康志愿者(正常对照组)的外周血,分离单个核细胞,提取总RNA,用实时定量PCR的方法检测Trx-1、Trx-2mRNA水平并进行统计分析。结果肝衰竭组患者PBMC中Trx-1、Trx-2的mRNA水平较慢性乙型肝炎组及正常对照组显著升高(P〈0.05)。同时,在肝衰竭患者中,Trx-1、Trx.2的mRNA水平与总胆红素水平(TBIL)呈正相关(P〈0.05)。Trx-1的mRNA水平与终末期肝病模型(MELD)评分呈正相关(P〈0.05)。此外,肝衰竭患者中死亡组Trx.1、Trx-2mRNA的水平较好转者明显上调(P〈0.05)。Kaplan—Meier分析表明,Trx.1mRNA水平较高的患者预后明显劣于Trx-1mRNA水平较低的患者(P〈0.05),其中Trx-1的截断值为0.635,敏感度为75%,特异度为64.29%。结论Trx-1、Trx-2mRNA及其反应的氧化损伤水平与肝衰竭的疾病严重程度和预后相关,并可能参与了疾病的发生和进展。Objective To investigate the role of Trx-1 and Trx-2 in the progression of hepatitis B associated acute-on-chronic liver failure (ACHBLF). Methods We determined the mRNA levels of Trx- 1, Trx-2 in peripheral blood mononuclear cells (PBMC) from a cohort of 60 patients with ACHBLF, 38 patients with chronic hepatitis B (CHB) and 26 healthy controls by fluorescence real-time quantiativc PCR. Results We demonstrated that there were significantly higher expressions of Trx-1 and Trx-2 mRNA in patients with ACHBLF than those patients with CHB and healthy controls ( P 〈 0.05, respectively). Furthermore, the levels of Trx-1 and Trx-2 mRNA significantly correlated with total bilirubin (TBIL) levels in patients with ACHBLF (P 〈 0.05, respectively). The relative expression of Trx-1 mRNA significantly correlated with model for end-stage liver disease (MELD) scores in patients with ACHBLF ( P 〈 0. 05 ). Besides, Trx-1 and Trx-2 levels were higher in non-survivors with ACHBLF than survivors with ACHBLF (P 〈0.05, respectively). The relative expression of Trx-I mRNA was predictive of 90-day mortality using Kaplan-Meier analysis (P 〈0. 05),with a sensitivity of 75% and a specificity of 64. 29%. Conclusion Trx and associated oxidative stress may play an important role in the pathogenesis and progression of ACHBLF, the mRNA level of Trx-1 and Trx-2 may be associated with disease severity and poor prognosis of ACHBLF.
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