用无创生化试验评价慢性乙型病毒性肝炎纤维化。

IF 1.2 Q4 GASTROENTEROLOGY & HEPATOLOGY
Adem Kaya, Sezgin Barutcu, Murat Taner Gulsen
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引用次数: 3

摘要

背景与目的:早期诊断和治疗慢性乙型肝炎(CHB)疾病对于预防肝硬化和肝细胞癌等并发症具有重要意义。肝活检是一种侵入性的、复杂的、昂贵的诊断方法,是检测纤维化的金标准。本研究的目的是探讨这些测试在预测肝纤维化和治疗决策中的作用。材料和方法:回顾性分析2010年至2020年加济安泰普大学消化内科诊断为慢性乙型肝炎的1051例患者。计算发病诊断时的AAR、API、APRI、FIB-4、KING评分、FIBROQ评分。此外,还确定了一个被认为更敏感、更具体的新公式——祖格玛分数。根据患者活检结果比较无创纤维化评分。结果:本研究中,API评分曲线下面积为0.648,APRI评分为0.711,FIB-4评分为0.716,KING评分为0.723,FIBROQ评分为0.595,Zeugma评分为0.701 (p)结论:KING评分是无创检测慢性HBV患者肝纤维化最可靠的方法。FIB-4、APRI和Zeugma评分在判断肝纤维化方面也被证明是有效的。结果表明,AAR评分不足以检测肝纤维化。Zeugma评分是一种新的无创测试,是一种有效且简单的工具,用于评估慢性HBV患者的肝纤维化,其准确性优于AAR、API和FIBROQ。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Evaluation of fibrosis with noninvasive biochemical tests in chronic viral hepatitis B.

Evaluation of fibrosis with noninvasive biochemical tests in chronic viral hepatitis B.

Evaluation of fibrosis with noninvasive biochemical tests in chronic viral hepatitis B.

Evaluation of fibrosis with noninvasive biochemical tests in chronic viral hepatitis B.

Background and aim: Early diagnosis and treatment of chronic hepatitis B (CHB) disease are important for the prevention of complications such as cirrhosis and hepatocellular cancer. Liver biopsy is an invasive, complicated, and expensive diagnostic method, which is the gold standard for detecting fibrosis. The aim of this study was to investigate the role of these tests in predicting liver fibrosis and treatment decision.

Materials and methods: A total of 1051 patients diagnosed with CHB between 2010 and 2020 in the Gaziantep University Gastroenterology Department were retrospectively evaluated. AAR, API, APRI, FIB-4, KING score, and FIBROQ score were calculated at the time of onset diagnosis. In addition, the Zeugma score, a new formula that is thought to be more sensitive and specific, was determined. Noninvasive fibrosis scores were compared according to the biopsy results of the patients.

Results: In this study, the area values under the curve were 0.648 for the API score, 0.711 for the APRI score, 0.716 for the FIB-4 score, 0.723 for the KING score, 0.595 for the FIBROQ score, and 0.701 for the Zeugma score (p<0.05). No statistically significant difference was obtained for the AAR score. The KING, FIB-4, APRI, and Zeugma scores were the best indicators for detecting advanced fibrosis. For KING, FIB-4, APRI, and Zeugma scores, the cutoff value for the prediction of advanced fibrosis were ≥8.67, ≥0.94, ≥16.24, and ≥9.63 with a sensitivity of 50.52%, 56.77%, 59.64%, and 52.34%, specificity of 87.26%, 74.96%, 73.61%, and 78.11%, respectively (p<0.05). In our study, we compared the globulin and GGT parameters with fibrosis, which we used in the Zeugma score formula. Globulin and GGT mean values were significantly higher in the fibrosis group (p<0.05). There was a statistically significant correlation between fibrosis and globulin and GGT values (p<0.05, r=0.230 and p<0.05, r=0.305, respectively).

Conclusion: The KING score was found to be the most reliable method for the noninvasive detection of hepatic fibrosis in patients with chronic HBV. The FIB-4, APRI, and Zeugma scores were also shown to be effective in determining liver fibrosis. It was shown that the AAR score was not sufficient for detecting hepatic fibrosis. The Zeugma score, a novel noninvasive test, is a useful and easy tool to evaluate liver fibrosis in patients with chronic HBV and has better accuracy than AAR, API, and FIBROQ.

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