Antiviral therapy response in patients with chronic hepatitis B and fatty liver: A systematic review and meta‐analysis

Author:

Rui Fajuan12,Garcia Elizabeth3,Hu Xinyu4,Ni Wenjing12,Xue Qi5,Xu Yayun4,Xu Xiaoming12,Shi Junping6,Nguyen Mindie H.78ORCID,Cheung Ramsey C.9,Li Jie12

Affiliation:

1. Department of Infectious Diseases Nanjing Drum Tower Hospital Clinical College of Nanjing University of Chinese Medicine Nanjing Jiangsu China

2. Department of Infectious Disease, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School Nanjing University Nanjing Jiangsu China

3. Stanford University Stanford, Palo Alto California USA

4. Department of Infectious Disease, Shandong Provincial Hospital Shandong University Ji'nan Shandong China

5. Department of Infectious Disease Shandong Provincial Hospital Affiliated to Shandong First Medical University Ji'nan Shandong China

6. Department of Infectious Diseases The Affiliated Hospital of Hangzhou Normal University Hangzhou Zhejiang China

7. Division of Gastroenterology and Hepatology Stanford University Medical Center Palo Alto California USA

8. Department of Epidemiology and Population Health Stanford University School of Medicine Palo Alto California USA

9. Department of Epidemiology and Population Health Veterans Affairs Medical Center Palo Alto California USA

Abstract

AbstractThe impact of concurrent fatty liver (FL) on response to antiviral therapy in chronic hepatitis B (CHB) patients has not been well characterized. We aimed to systematically review and analyse antiviral treatment response in CHB patients with and without FL. We searched PubMed, Embase, Web of Science and the Cochrane Library databases from inception to 31 May 2023 for relevant studies. Biochemical response (BR), complete viral suppression (CVS) and hepatitis B e antigen (HBeAg) seroconversion in CHB patients with FL (CHB‐FL) and without FL (non‐FL CHB) were compared. In an initial pool of 2101 citations, a total of 10 studies involving 2108 patients were included. After 12 weeks of treatment, CHB‐FL patients as compared with non‐FL CHB patients had lower BR rate (48.37% [108/227] vs. 72.98% [126/174], p = .04) but similar trend for CVS (36.86% [80/227] vs. 68.81% [114/174], p = .05) and similar rates of HBeAg seroconversion (6.59% [7/103] vs. 7.40% [7/110], p = .89). However, at week 48, there were no statistically significant differences between CHB‐FL and non‐FL CHB patients in any of the outcomes, including BR (60.03% [213/471] vs. 69.37% [314/717], p = .67), CVS (65.63% [459/746] vs. 73.81% [743/1132], p = .27) and HBeAg seroconversion (10.01% [30/275] vs. 14.06% [65/453], p = .58) with similar findings for week 96. BR rate was lower in CHB‐FL patients after 12 weeks of antiviral treatment. However, after a longer follow‐up of either 48 or 96 weeks, no statistically significant differences were observed in BR, CVS or HBeAg seroconversion rates between CHB patients with and without FL.

Publisher

Wiley

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