Abstract

目的 肝纤维化程度的评估对于指导慢性乙型肝炎患者治疗及预测预后具有重要意义,本研究旨在评价LPRI评分对乙型肝炎肝纤维化/肝硬化初治人群的诊断价值。 方法 筛选首都医科大学附属北京友谊医院既往乙型肝炎研究队列2013年6月—2015年9月经肝穿刺确诊的慢性乙型肝炎患者276例。基于患者肝脏硬度测定(LSM)联合PLT计算LPRI评分,以肝脏病理为金标准,评价LPRI评分对于乙型肝炎肝纤维化及肝硬化的诊断价值。不符合正态分布计量资料多组间比较采用Kruskal-Wallis H秩和检验,计数资料组间比较采用χ2检验。各诊断模型与肝穿病理的相关性分析采用Spearman相关分析;通过DeLong法比较多个无创诊断模型(LPRI、LSM、APRI、FIB-4)的受试者工作特征曲线下面积(AUC)及诊断性能。采用Bootstrap方法对LPRI肝纤维化/肝硬化的诊断价值进行内部验证。 结果 根据肝纤维化程度的不同,分为F0/1组(n=63)、F2/3组(n=118)、F4组(n=95),3组间Alb、TBil、PLT、LSM、AFP及HBV DNA水平均具有统计学差异(P值均<0.05)。LPRI评分与肝穿病理有较好的相关性(r=0.501,P<0.001);对乙型肝炎显著性肝纤维化(AUC=0.88, 95%CI: 0.83~0.91)的诊断性能优于肝硬化(AUC=0.79, 95%CI: 0.73~0.83)。相比APRI评分和FIB-4指数,LPRI的诊断性能更好(P值均<0.05);与LSM联合后,LPRI评分能进一步补充LSM对肝硬化诊断的灵敏度(53%提高至82%)。经约登指数推荐的诊断显著性肝纤维化和肝硬化的LPRI评分界值分别为6.1(灵敏度71%,特异度92%)和6.9(灵敏度81%,特异度66%)。 结论 LPRI评分作为一种简易方便的肝纤维化无创诊断指数,在慢性乙型肝炎患者肝纤维化/肝硬化的诊断和分期中有一定的应用价值。

Alternate abstract:

Objective To investigate the diagnostic value of liver stiffness measurement-to-platelet ratio index (LPRI) score in previously untreated patients with hepatitis B liver fibrosis/liver cirrhosis, since the evaluation of liver fibrosis degree has great significance in guiding the treatment of chronic hepatitis B patients and predicting their prognosis. Methods A total of 276 chronic hepatitis B patients who were diagnosed by liver biopsy from June 2013 to September 2015 were selected from the hepatitis B study cohort of Beijing Friendship Hospital, Capital Medical University. LPRI score was calculated based on liver stiffness measurement (LSM) and platelet, and the value of LPRI score in the diagnosis of liver fibrosis and liver cirrhosis in hepatitis B patients was evaluated with liver pathology as the gold standard. The Kruskal-Wallis H test was used for comparison of non-normally distributed continuous data between multiple groups, and the chi-square test was used for comparison of categorical data between groups. A Spearman correlation analysis was used to investigate the correlation between each diagnostic model and liver biopsy, and the DeLong test was used to compare the area under the ROC curve (AUC) and diagnostic performance of several noninvasive diagnostic models, i.e., LPRI, LSM, aspartate aminotransferase-to-platelet ratio index (APRI), and fibrosis-4 (FIB-4). The Bootstrap method was used for the internal validation of the value of LPRI score in the diagnosis of liver fibrosis/cirrhosis. Results According to the stage of liver fibrosis, the patients were divided into F0/1 group with 63 patients, F2/3 group with 118 patients, and F4 group with 95 patients, and there were significant differences in albumin, total bilirubin, platelet count, LSM, alpha-fetoprotein, and HBV DNA between the three groups (all P < 0.05). LPRI score was significantly correlated with liver biopsy (r=0.501, P < 0.001); LPRI score had an AUC of 0.88 (95% confidence interval [CI]: 0.83-0.91) in the diagnosis of liver fibrosis and an AUC of 0.79 (95% CI: 0.73-0.83) in the diagnosis of liver cirrhosis, suggesting that the diagnostic performance of LPRI score for significant liver fibrosis was better than that for liver cirrhosis. LPRI had a better diagnostic performance than APRI and FIB-4 (both P < 0.05), and in combination with LSM, LPRI score further supplemented the sensitivity of LSM in the diagnosis of liver cirrhosis, with an increase from 53% to 82%. The cut-off values of LPRI score recommended by Youden index were 6.1 (with a sensitivity of 71% and a specificity of 92%) for significant liver fibrosis and 6.9 (with a sensitivity of 81% and a specificity of 66%) for liver cirrhosis. Conclusion As a simple and convenient noninvasive diagnostic index for liver fibrosis, LPRI score has a certain application value in the diagnosis and staging of liver fibrosis and liver cirrhosis in chronic hepatitis B patients.

Details

Title
LPRI评分在乙型肝炎肝纤维化及肝硬化中的诊断价值
Author
周家玲; 王冰琼; 孙亚朦; 孟彤彤; 武珊珊; 马红; 欧晓娟; 尤红; 贾继东; 吴晓宁  VIAFID ORCID Logo 
Pages
1529-1533
Section
Original Articles_Liver Fibrosis and Liver Cirrhosis
Publication year
2022
Publication date
2022
Publisher
Journal of Clinical Hepatology
ISSN
10015256
e-ISSN
20973497
Source type
Scholarly Journal
Language of publication
Chinese
ProQuest document ID
3239375695
Copyright
© 2022. This work is published under https://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.