Genetic polymorphisms of interleukin‐1‐beta in association with sustained response to anti‐viral treatment in chronic hepatitis B in Chinese

Summary Background Interleukin‐1β is a pro‐inflammatory cytokine that may influence host defence against viral infection. Aim To investigate the impact of interleukin‐1β gene polymorphism on the response to anti‐viral treatment. Method Hepatitis B e antigen‐positive chronic hepatitis B patients who...

Full description

Saved in:
Bibliographic Details
Published inAlimentary pharmacology & therapeutics Vol. 23; no. 12; pp. 1703 - 1711
Main Authors CHAN, H. L.‐Y., TSE, A. M.‐L., ZHANG, M.‐D., WONG, V. W.‐S., CHIM, A. M.‐L., HUI, A. Y., SUNG, J. J.‐Y.
Format Journal Article
LanguageEnglish
Published Oxford, UK Blackwell Publishing Ltd 01.06.2006
Blackwell
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Summary Background Interleukin‐1β is a pro‐inflammatory cytokine that may influence host defence against viral infection. Aim To investigate the impact of interleukin‐1β gene polymorphism on the response to anti‐viral treatment. Method Hepatitis B e antigen‐positive chronic hepatitis B patients who have completed a randomized study of peginterferon alpha‐2b and lamivudine combination vs. lamivudine monotherapy were included. Sustained responders were patients who had persistent hepatitis B e antigen loss and less than two occasions with hepatitis B virus DNA >100 000 copies/mL at any time up to week 76 post‐treatment. Polymorphisms at interleukin‐1β‐511, ‐31 and ‐3954 and interleukin‐1 receptor antagonist (RN) were studied. Results Eighty‐eight patients were studied and 18 (20%) patients developed sustained response. Near complete linkage disequilibrium was observed between interleukin‐1β‐511 and ‐31 loci. After adjustment for the potential confounding effects of treatment allocation, hepatitis B virus genotype, pre‐treatment alanine aminotransferase and hepatitis B virus DNA levels, genotype C/T at interleukin‐1β‐511 was found to be associated with higher sustained response than genotype C/C (adjusted odds ratio 10.4, 95% CI 1.1, 96.9, P = 0.040). The proportion of sustained responders tend to be higher among patients with allele T at interleukin‐1β‐511 (83%) than those without (70%) (P = 0.058). Conclusion High interleukin‐1β production genotype at position ‐511 has a favourable response to anti‐viral treatments.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ObjectType-Article-2
ObjectType-News-1
ObjectType-Feature-3
ISSN:0269-2813
1365-2036
DOI:10.1111/j.1365-2036.2006.02948.x