Abstract
Sensitive polymerase chain reaction assays to measure hepatitis B virus (HBV) DNA became only available the last decade. Hence, the long-term outcome of Caucasian patients in Western Europe with hepatitis B e antigen (HBeAg)-negative chronic infection, especially with a baseline HBV DNA level > 2000 IU/mL, is still unclear. Out of a cohort of 1936 chronic HBV patients, 413 Caucasian individuals were identified with HBeAg-negative chronic infection, defined as persistently normal alanine aminotransferase (ALT) levels and HBV DNA levels 2 x upper limit of normal due to non-HBV-related causes. The cumulative probability of spontaneously developing CAH after 10 years was almost exclusively seen in patients with baseline HBV DNA level > 2000 IU/mL (11.7% vs 1.2%; P <.001). Advanced liver disease developed significantly more in patients with baseline HBV DNA level > 2000 IU/mL (5.2% vs 1.5%; P = .018) and occurred especially in patients with obesity (16.7% vs 4.2%; P = .049). The incidence of hepatocellular carcinoma was 0.0%. Caucasian patients with HBeAg-negative chronic infection and baseline HBV DNA level 2000 IU/mL are at risk to develop advanced liver disease.
Original language | English |
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Pages (from-to) | 3373-3380 |
Number of pages | 8 |
Journal | Journal of Medical Virology |
Volume | 92 |
Issue number | 12 |
Early online date | 12 May 2020 |
DOIs | |
Publication status | Published - Dec 2020 |
Keywords
- alanine aminotransferase
- Caucasian race
- chronic hepatitis B
- HBeAg-negative chronic infection
- HBV DNA
- inactive HBV carrier
- PERSISTENTLY NORMAL ALT
- HBV DNA LEVELS
- NATURAL-HISTORY
- FOLLOW-UP
- VIRUS-INFECTION
- CARRIERS
- REACTIVATION
- MANAGEMENT
- RISK