4.3 Article

Clinical Course of Hepatitis B Viral Infection in Patients Undergoing Anti-Tumor Necrosis Factor a Therapy for Inflammatory Bowel Disease

Journal

GUT AND LIVER
Volume 16, Issue 3, Pages 396-403

Publisher

EDITORIAL OFFICE GUT & LIVER
DOI: 10.5009/gnl210081

Keywords

Hepatitis B virus; Reactivation; Inflammatory bowel disease; Anti-tumor necrosis factor alpha

Funding

  1. Asian Organization for Crohn's and Colitis

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This study investigated the clinical course and liver dysfunction risks in HBV-infected IBD patients undergoing anti-TNF-alpha therapy. The results showed that liver dysfunction due to HBV reactivation was more common in patients with chronic HBV infection. Antiviral prophylaxis significantly reduced the risk of liver dysfunction in patients with chronic HBV infection.
Background/Aims: Little is known about the clinical course of hepatitis B virus (HBV)-infected patients undergoing anti-tumor necrosis factor a (TNF-alpha) therapy for inflammatory bowel disease (IBD). We aimed to investigate the clinical course of HBV infection and IBD and to analyze liver dysfunction risks in patients undergoing anti-TNF-alpha therapy. Methods: This retrospective multinational study involved multiple centers in Korea, China, Taiwan, and Japan. We enrolled IBD patients with chronic or resolved HBV infection, who received anti-TNF-alpha therapy. The patients' medical records were reviewed, and data were collected using a web-based case report form. Results: Overall, 191 patients (77 ulcerative colitis and 114 Crohn's disease) were included, 28.3% of whom received prophylactic antivirals. During a median follow-up duration of 32.4 months, 7.3% of patients experienced liver dysfunction due to HBV reactivation. Among patients with chronic HBV infection, the proportion experiencing liver dysfunction was significantly higher in the non-prophylaxis group (26% vs 8%, p=0.02). Liver dysfunction occurred in one patient with resolved HBV infection. Antiviral prophylaxis was independently associated with an 84% reduction in liver dysfunction risk in patients with chronic HBV infection (odds ratio, 0.16; 95% confidence interval, 0.04 to 0.66; p=0.01). The clinical course of IBD was not associated with liver dysfunction or the administration of antiviral prophylaxis. Conclusions: Liver dysfunction due to HBV reactivation can occur in HBV-infected IBD patients treated with anti-TNF-alpha agents. Careful monitoring is needed in these patients, and antivirals should be administered, especially to those with chronic HBV infection. (Gut Liver 2022;16:396403)

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