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评价 HBeAg 阴性患者的前基因组 HBV RNA。

Evaluation of pregenomic HBV RNA in HBeAg-negative patients.

机构信息

Operative Unit of Clinical Microbiology, IRCCS S. Orsola-Malpighi University Hospital, Bologna, Italy

Microbiology, DIMES, University of Bologna, Italy

出版信息

New Microbiol. 2022 Apr;45(2):104-110.

Abstract

The distinction between chronic HBeAg-negative hepatitis (CHB) and chronic HBeAg-negative infection (CIB) can be challenging and important for providing advice on prognosis, as well as determining need for treatment. The aim of the present study was to evaluate pgRNA levels in treatment-naïve HBeAg-negative chronic HBV-infected patients. In addition, pgRNA levels were compared to traditional markers in order to assess their clinical utility. A retrospective study was carried out, including 85 cases of CHBs and 74 CIBs. Globally, when the virological markers (pgRNA, qHBsAg, and HBV DNA) were analyzed, significant differences were found between the CHB and CIB groups (P<0.001). Overall, positive correlations were demonstrated, as follows: between pgRNA levels and qHBsAg (Spearman r=0.30, P<0.001), between pgRNA and HBV DNA (Spearman r=0.73, P<0.001), and between pgRNA and ALT (Spearman r=0.67, P<0.001). Out of the 85 CHB patients, 82 (96.5%) agreed to start treatment. At baseline, 38/82 patients, as well as the 3 untreated CHB patients, had undetectable pgRNA levels. The 74 CIB carriers also had undetectable pgRNA levels. During the follow-up period, no patients experienced viral reactivation or progression of liver disease. These results suggest that the addition of plasmatic HBV-pgRNA levels to the traditional diagnostic flowchart of HBeAg-negative patients may improve the correct identification of cases at risk, especially patients with occasional increases in HBV viremia.

摘要

慢性 HBeAg 阴性肝炎 (CHB) 和慢性 HBeAg 阴性感染 (CIB) 的区分具有一定挑战性,对提供预后建议以及确定治疗需求非常重要。本研究旨在评估未经治疗的 HBeAg 阴性慢性乙型肝炎病毒感染患者的 pgRNA 水平,并将其与传统标志物进行比较,以评估其临床应用价值。本研究为回顾性研究,共纳入 85 例 CHB 患者和 74 例 CIB 患者。总体而言,在分析病毒学标志物(pgRNA、qHBsAg 和 HBV DNA)时,CHB 组和 CIB 组之间存在显著差异(P<0.001)。总体上,pgRNA 水平与 qHBsAg(Spearman r=0.30,P<0.001)、pgRNA 与 HBV DNA(Spearman r=0.73,P<0.001)和 pgRNA 与 ALT(Spearman r=0.67,P<0.001)之间存在正相关。在 85 例 CHB 患者中,82 例(96.5%)同意开始治疗。在基线时,82 例中有 38 例(46.3%)和 3 例未经治疗的 CHB 患者 pgRNA 水平不可检测。74 例 CIB 携带者 pgRNA 水平也不可检测。在随访期间,无患者出现病毒再激活或肝病进展。这些结果表明,在 HBeAg 阴性患者的传统诊断流程图中加入血浆 HBV-pgRNA 水平可能有助于更准确地识别高危病例,特别是偶尔出现 HBV 病毒血症升高的病例。

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