Antiviral therapy reduces portal pressure in patients with cirrhosis due to HBeAg-negative chronic hepatitis B and significant portal hypertension

J Hepatol. 2009 Sep;51(3):468-74. doi: 10.1016/j.jhep.2009.05.031. Epub 2009 Jul 3.

Abstract

Background/aims: Lamivudine improves liver histology in patients with chronic hepatitis B (CHB), but its effects on portal pressure remain unknown. We evaluated the effect of lamivudine monotherapy on hepatic venous pressure gradient (HVPG) in CHB-related cirrhosis with significant portal hypertension.

Methods: We studied 19 patients with cirrhosis due to HBeAg-negative CHB and HVPG >or=10 mm Hg treated with oral lamivudine (100mg daily). Liver biochemistry, Child-Pugh and MELD score were determined every 3 months, alpha-fetoprotein and HBV DNA every 6 months and HVPG at baseline and at 12 months after lamivudine initiation. Diuretics, beta-blockers, antibiotics and/or endoscopic therapy were used for routine indications.

Results: At 12 months, a significant reduction was observed in ALT (p=0.001), HBV DNA (p=0.002), Child-Pugh (p=0.012) and MELD score (p=0.006). Four patients developed virological breakthrough during treatment. At 12 months, HVPG decreased in all but one patient [baseline: 14.4+/-3.9 and 12 months: 12.4+/-3.3 mm Hg (p=0.007)]. HVPG decreased >20% or below the 12 mm Hg threshold in 10 of 13 patients with baseline HVPG >or=12 mm Hg. HVPG increased in a patient with hepatic flare after virological breakthrough.

Conclusion: In conclusion, in patients with cirrhosis due to HBeAg-negative CHB, lamivudine monotherapy reduces HVPG, especially when virological suppression and biochemical remission is achieved.

MeSH terms

  • Administration, Oral
  • Adult
  • Aged
  • Alanine Transaminase / metabolism
  • Antiviral Agents / administration & dosage
  • Antiviral Agents / pharmacology
  • Antiviral Agents / therapeutic use
  • Biomarkers
  • DNA, Viral / blood
  • Female
  • Follow-Up Studies
  • Hepatitis B e Antigens / metabolism*
  • Hepatitis B, Chronic / complications*
  • Hepatitis B, Chronic / immunology*
  • Hepatitis B, Chronic / physiopathology
  • Humans
  • Hypertension, Portal / complications*
  • Hypertension, Portal / drug therapy
  • Hypertension, Portal / physiopathology
  • Lamivudine / administration & dosage
  • Lamivudine / pharmacology*
  • Lamivudine / therapeutic use
  • Liver / metabolism
  • Liver Cirrhosis / drug therapy
  • Liver Cirrhosis / etiology*
  • Liver Cirrhosis / physiopathology*
  • Male
  • Middle Aged
  • Portal Pressure / drug effects*
  • Portal Pressure / physiology
  • Prognosis
  • Prospective Studies
  • Treatment Outcome
  • alpha-Fetoproteins / metabolism

Substances

  • Antiviral Agents
  • Biomarkers
  • DNA, Viral
  • Hepatitis B e Antigens
  • alpha-Fetoproteins
  • Lamivudine
  • Alanine Transaminase