临床外科杂志 ›› 2024, Vol. 32 ›› Issue (3): 281-284.doi: 10.3969/j.issn.1005-6483.2024.03.017

• 论著 • 上一篇    下一篇

肝硬化病人血清lncRNA TUG1表达水平与肝功能、肝纤维化程度的相关性研究

李轶 尚立   

  1. 710054 西安市第九医院血管介入科(李轶),消化内科(尚立)
  • 收稿日期:2023-02-15 出版日期:2024-03-20 发布日期:2024-03-20
  • 通讯作者: 尚立,Email:bwwyukvhcui35@163.com
  • 基金资助:
    西安市第九医院科研项目(编号:2020-7)

Study on the correlation of serum lncRNA TUG1 expression level with liver function and degree of liver fibrosis in patients with liver cirrhosis

LI Yi,SHANG Li   

  1. Department of Vascular Interventional,Xi’an Ninth Hospital,Shaanxi,Xi’an 710054,China
  • Received:2023-02-15 Online:2024-03-20 Published:2024-03-20

摘要: 目的 探讨肝硬化病人血清长链非编码RNA牛磺酸上调基因1(lncRNA TUG1)表达情况及其与肝功能、肝纤维化程度的相关性。方法 选取2020年2月~2022年6月本院收治的乙型肝炎肝硬化病人92例为肝硬化组,均为Child-Pugh分级C级,根据肝纤维化程度分为轻中度组和重度组;同期88例本院健康体检者为对照组。采用荧光定量PCR(qRT-PCR)法测定血清lncRNA TUG1水平,采用全自动生化分析仪测定肝功能指标血清丙氨酸氨基转移酶(ALT)、天冬氨酸氨基转移酶(AST)、总胆红素(TBIL)水平,采用酶联免疫吸附(ELISA)法测定肝纤维化指标层黏连蛋白(LN)、Ⅲ型前胶原肽(PⅢP)、Ⅳ型胶原(CⅣ)水平;采用Pearson相关分析肝硬化病人血清lncRNA TUG1与肝功能指标、肝纤维化指标的相关性;绘制受试者工作特征(ROC)曲线分析血清lncRNA TUG1水平对肝硬化病人肝纤维化程度的评估效能;采用多元Logistic回归分析影响肝硬化病人肝纤维化程度的因素。结果 肝硬化组血清lncRNA TUG1、ALT、AST、TBIL、LN、PⅢP、CⅣ水平均显著高于对照组(P<0.001)。重度组肝硬化病程、HBV DNA、lncRNA TUG1、ALT、AST、TBIL、LN、PⅢP、CⅣ均显著高于轻中度组,差异有统计学意义(P<0.05)。肝硬化病人血清lncRNA TUG1与HBV DNA、ALT、AST、TBIL、LN、PⅢP、CⅣ均呈正相关(r:0.54、0.50、0.49、0.50、0.51、0.52、0.52,P<0.05)。lncRNA TUG1评估肝硬化病人肝纤维化程度发展为重度的曲线下面积(AUC)为0.91,截断点为2.61。lncRNA TUG1、LN与肝硬化病人肝纤维化程度发展为重度有关(P<0.05)。结论 血清lncRNA TUG1水平与肝硬化病人肝功能、肝纤维化程度均相关,检测血清lncRNA TUG1水平有利于评估病人肝纤维化的发展趋势。

关键词: 肝硬化;长链非编码RNA牛磺酸上调基因1;肝功能;肝纤维化程度

Abstract: Objective To investigate the expression of serum long non-coding ribonucleic acid taurine up-regulated gene 1 (lncRNA TUG1) in patients with liver cirrhosis and its correlation with liver function and liver fibrosis.Methods From February 2020 to June 22,92 patients with Hepatitis B cirrhosis of Child-Pugh grade C in our hospital were selected as the liver cirrhosis group,their general data were recorded,and they were grouped into mild-to-moderate group and severe group according to the degree of liver fibrosis;88 healthy subjects in our hospital were the control group.The level of serum lncRNA TUG1 was determined by fluorescence quantitative PCR (qRT-PCR),an automatic biochemical analyzer was applied to measure the levels of serum alanine aminotransferase (ALT),aspartate aminotransferase (AST),and total bilirubin (TBIL),the levels of laminin (LN),type Ⅲ procollagen peptide (PⅢP),and type Ⅳ collagen (CⅣ) were determined by ELISA;Pearson correlation was applied to analyze the correlation of serum lncRNA TUG1 with liver function indexes and liver fibrosis indexes in patients with liver cirrhosis;receiver operating characteristic (ROC) curve was drawn to analyze the efficacy of serum lncRNA TUG1 level in evaluating the degree of liver fibrosis in patients with liver cirrhosis;Multivariate stepwise regression analysis of factors affecting the degree of liver fibrosis in patients with cirrhosis.Results The levels of serum lncRNA TUG1,ALT,AST,TBIL,LN,PⅢP and CⅣ in the liver cirrhosis group were obviously higher than those in the control group (P<0.001).The course of liver cirrhosis,lncRNA TUG1,HBV DNA,ALT,AST,TBIL,LN,PⅢP,and CⅣ in the severe group were obviously higher than those in the mild-moderate group (P<0.05).Serum lncRNA TUG1 in patients with liver cirrhosis was positively correlated with HBV DNA,ALT,AST,TBIL,LN,PⅢP,and CⅣ (r:0.54、0.50、0.49、0.50、0.51、0.52、0.52,P<0.05).The area under the curve (AUC) of lncRNA TUG1 to evaluate the development of severe liver fibrosis in patients with liver cirrhosis was 0.91,the cutoff is 2.61.The lncRNA TUG1 and LN are related to the degree of liver fibrosis in patients with cirrhosis (P<0.05).Conclusion Serum lncRNA TUG1 level is correlated with liver function and degree of liver fibrosis in patients with liver cirrhosis.Detection of serum lncRNA TUG1 level is helpful for evaluating the development trend of liver fibrosis in patients.

Key words: liver cirrhosis; long non-coding ribonucleic acid taurine up-regulated gene 1; liver function; liver fibrosis degree

No related articles found!
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!