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Significant prevalence of histologic disease in patients with chronic hepatitis B and mildly elevated serum alanine aminotransferase levels

Authors :
Mindie H. Nguyen
Huy A. Nguyen
Philip S.Y. Tsang
Nghiem B. Ha
Huy N. Trinh
Ruel T. Garcia
Emmet B. Keeffe
Jeanine T. Phan
Khanh K. Nguyen
Source :
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association. 6(5)
Publication Year :
2008

Abstract

Background & Aims: Serum ALT remains the most accessible test available to clinicians for monitoring chronic hepatitis B virus infection, but appropriate action when ALT levels are only mildly elevated is ambiguous in standard guidelines. Methods: A retrospective study was conducted to investigate the prevalence of significant histology in a patient population with mildly elevated serum ALT levels. A total of 193 consecutive patients were selected and divided into 2 groups according to HBeAg status. Patients were further divided into cohorts on the basis of their highest ALT elevation during follow-up and whether it was 1–1.5 times the upper limit of normal (ULN), 1.5–2 times the ULN, or greater than twice the ULN. The ULN that was used is 30 U/L for men and 19 U/L for women. Results: In all cohorts there was a substantial fraction of patients with histologic disease as evaluated by liver biopsy. HBeAg-negative patients were older, had lower viral load, and had a higher prevalence of disease. After adjustments for age, HBeAg status and HBV DNA viral load were not predictors of significant histology. Age >35 years, male gender, and increasing ALT levels were predictors for significant histology on multivariate analysis. Conclusions: A substantial proportion of patients with mildly elevated ALT levels have significant histologic disease. The prevalence increased with the higher ALT levels and age.

Details

ISSN :
15427714
Volume :
6
Issue :
5
Database :
OpenAIRE
Journal :
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association
Accession number :
edsair.doi.dedup.....72fe8887f6257a8c784d982c95be614e