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Anti-viral effect in chronic hepatitis B patients with normal or mildly elevated alanine aminotransferase
Qingqing Zhao 1 , Kehui Liu 2 , Xiaojun Zhu 3 , Lei Yan 1 , Yezhou Ding 1 , Yumin Xu 1 , Shike Lou 1 , Gangde Zhao 1 , Qing Xie 1 , Yueqiu Gao 4 , Shisan Bao 5 , Hui Wang 6
Affiliations
Affiliations
1
Department of Infectious Diseases, Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China.
2
Department of Infectious Diseases, Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China; Department of Infectious Diseases, Rui Jin North Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 201801, China.
3
Department of Hepatopathy, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China.
4
Department of Hepatopathy, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, China. Electronic address: [email protected].
5
Discipline of Pathology, School of Medical Sciences, Faculty of Medicine and Sciences, University of Sydney, Sydney, NSW, 2006, Australia. Electronic address: [email protected].
6
Department of Infectious Diseases, Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China. Electronic address: [email protected].
PMID: 33065138 DOI: 10.1016/j.antiviral.2020.104953
Abstract
Background & aims: Normal/mildly elevated ALT (<2×ULN) CHB patients are potentially at risk of progression to cirrhosis and/or hepatocellular carcinoma (HCC). We aimed to assess the outcomes of anti-viral therapy for normal/mild elevation of ALT CHB patients. CHB patients (n=432) were liver biopsied was determined.
Methods: It was determined that the outcomes of anti-viral therapy in CHB patients with normal/mild elevation of ALT, in response to nucleoside/nucleotide analogues (NAs) (n=190) and pegylated interferon (PEG-IFN) (n=30) treatment for up to 72 weeks. Non-antiviral treated patients were used as control (n=40).
Results: There was about 50% of the CHB patients showed hepatic inflammatory necrosis ≥ G2 and/or fibrosis ≥ S2, and were >30-years. The rate of undetectable HBV DNA in NAs and PEG-IFN groups was ∼50%, ∼80% or ∼90% at week 24, 48 or 72, respectively. HBeAg clearance rate was lower in NAs treated than that in PEG-IFN group at week 48 (6% vs 20%, P<0.05). ALT normalization rate was increased by 1.18-fold at week 72. HBsAg decline in HBeAg+ patients treated with NAs or PEG-IFN was 0.418 or 1.217 log IU/mL (P<0.0001) at week 48; whereas HBsAg decline was 0.176 or 0.816 log IU/mL (P<0.001) in HBeAg- patients. HBsAg at baseline and week 24 were strong predictors of "low HBsAg at week 48".
Conclusion: Long term antiviral therapy inhibits HBV replication effectively in ALT<2×ULN CHB patients. PEG-IFN therapy is recommended for HBeAg+ patients with baseline HBsAg<4.37 log IU/ml and HBeAg- patients with baseline HBsAg<2.66 log IU/ml to achieve "low HBsAg at week 48".
Keywords: ALT; Chronic hepatitis B; HBV DNA; HBsAg; NAs; PEG-IFN.
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