Literature DB >> 25014234

Residual amount of HBV DNA in serum is related to relapse in chronic hepatitis B patients after cessation of nucleos(t)ide analogs.

Jian-ning Jiang1, Zhan-lian Huang, Li-xia He, Yue-hua Huang, Ming-hua Su, Rong Xie, Yan-xiu Liang, Wu-dao Fu, Xiao-hong Huang, Wen-wen Guo, Shao-hua Zhong, Zhi-hong Liu, Shi-hua Li, Tuo-fu Zhu, Zhi-liang Gao.   

Abstract

OBJECTIVE: To investigate the relationship between relapse and the levels of the residual amount of HBV DNA in serum at cessation in chronic hepatitis B patients meeting 2008 Asian Pacific Association for the Study of the Liver (APASL) nucleos(t)ide analogs (NAs) cessation criteria.
METHODS: A total of 72 chronic hepatitis B patients who took NAs and had reached 2008 APASL cessation criteria entered the study. Patients were followed up for 6 months or longer after antiviral therapy was stopped. Serum HBV DNA level at cessation was detected by a highly sensitive polymerase chain reaction assay with detection limitation of 2 IU/mL.
RESULTS: Of all the 72 patients, 42 patients (65.3%) relapsed after NA cessation. The detectable rate of the trace amount of HBV DNA at cessation was 41.7% by highly sensitive polymerase chain reaction reagents. The detectable rate of patients with consolidation treatment duration of <18 months was higher than that with consolidation duration of ≥18 months (47.5% vs. 15.4%, P=0.034), and the detectable rate of patients with HBeAg seroconversion within 6 months of treatment was lower than that of ≥6 months (25.0% vs. 61.5%, P=0.036). The residual amount of HBV DNA and detectable rate at cessation showed significant differences between relapsed and nonrelapsed patients (130.4±420.90 vs 44.6±155.16 IU/mL, P=0.004; 55.3% vs. 16.0%, P=0.001). The cutoff value predicting relapse was 2.24 IU/mL, with a sensitivity of 0.553 and specificity of 0.840.
CONCLUSIONS: Residual amount of HBV DNA in serum at NA cessation is associated with HBV relapse. The cutoff value predicting relapse was 2.24 IU/mL, with a sensitivity of 0.553 and specificity of 0.840.

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Year:  2015        PMID: 25014234     DOI: 10.1097/MCG.0000000000000170

Source DB:  PubMed          Journal:  J Clin Gastroenterol        ISSN: 0192-0790            Impact factor:   3.062


  5 in total

1.  Comparison of the QIAGEN artus HBV QS-RGQ Assay With the Roche COBAS AmpliPrep/COBAS TaqMan HBV Assay for Quantifying Viral DNA in Sera of Chronic Hepatitis B Patients.

Authors:  Mi Soon Han; Yongjung Park; Hyunjin Nah; Hyon Suk Kim
Journal:  Ann Lab Med       Date:  2017-05       Impact factor: 3.464

2.  Performance Comparison of the artus HBV QS-RGQ and the CAP/CTM HBV v2.0 Assays regarding Hepatitis B Virus DNA Quantification.

Authors:  Salma Madihi; Hashim Syed; Fatiha Lazar; Abdelmajid Zyad; Abdelouaheb Benani
Journal:  Biomed Res Int       Date:  2020-04-14       Impact factor: 3.411

Review 3.  Risks and Benefits of Discontinuation of Nucleos(t)ide Analogue Treatment: A Treatment Concept for Patients With HBeAg-Negative Chronic Hepatitis B.

Authors:  Florian van Bömmel; Thomas Berg
Journal:  Hepatol Commun       Date:  2021-06-18

Review 4.  Review of Laboratory Tests used in Monitoring Hepatitis B Response to Pegylated Interferon and Nucleos(t)ide Analog Therapy.

Authors:  Carla Osiowy; Carla Coffin; Anton Andonov
Journal:  Curr Treat Options Infect Dis       Date:  2016-07-02

Review 5.  Is it possible to stop nucleos(t)ide analogue treatment in chronic hepatitis B patients?

Authors:  Elia Moreno-Cubero; Robert T Sánchez Del Arco; Julia Peña-Asensio; Eduardo Sanz de Villalobos; Joaquín Míquel; Juan Ramón Larrubia
Journal:  World J Gastroenterol       Date:  2018-05-07       Impact factor: 5.742

  5 in total

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