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Statins associate with better clinical outcomes in chronic hepatitis B patients with HBsAg seroclearance
Ka Shing Cheung1,2, Lung Yi Mak1, Lok Ka Lam1
1Department of Medicine, Queen Mary Hospital, The University of Hong Kong, Hong Kong, China.
Insights
Long-term outcomes for chronic hepatitis B (CHB) patients after HBsAg seroclearance are generally favorable. However, statin use was associated with significantly reduced risks of cirrhosis, hepatocellular carcinoma (HCC), and all-cause mortality.
Area of Science:
- Hepatology
- Clinical Medicine
- Virology
Background:
- Chronic hepatitis B (CHB) is a significant global health concern.
- Hepatitis B surface antigen (HBsAg) seroclearance marks a milestone in CHB management.
- Long-term outcomes post-HBsAg seroclearance require detailed characterization.
Purpose of the Study:
- To elucidate long-term clinical outcomes in CHB patients following HBsAg seroclearance.
- To identify factors influencing disease progression and adverse events.
- To investigate the potential benefits of statin therapy in this patient cohort.
Main Methods:
- Retrospective cohort study of CHB patients with HBsAg seroclearance (1986-2017).
- Primary outcomes: cirrhosis and hepatocellular carcinoma (HCC). Secondary outcomes: hepatic decompensation, liver-related death/transplantation, and all-cause mortality.
- Multivariable Cox regression and propensity score matching (PSM) were employed to analyze outcomes, including the effect of statin use.
Main Results:
- Statins significantly reduced the risk of cirrhosis/HCC (aHR: 0.44) and all-cause mortality (aHR: 0.21).
- Statin users experienced no hepatic decompensation or liver-related death/transplantation.
- Factors associated with increased cirrhosis/HCC risk included older age, diabetes, elevated creatinine, GGT, and AFP levels.
Conclusions:
- CHB patients achieving HBsAg seroclearance exhibit favorable long-term survival.
- Despite favorable outcomes, liver-related adverse events can still occur.
- Further research into the beneficial effects of statins in CHB patients post-seroclearance is warranted.
Introduction:
We aimed to describe long-term clinical outcomes in chronic hepatitis B (CHB) patients after HBsAg seroclearance, and identify factors that modify disease outcomes.
Methods:
CHB patients with HBsAg seroclearance occurring between 1986 and 2017 were recruited. Primary outcome was cirrhosis/hepatocellular carcinoma (HCC), and secondary outcomes were hepatic decompensation, liver-related death/transplantation, and all-cause mortality. Multivariable Cox model included demographics, prior antivirals, comorbidities, drugs (statins, metformin, proton-pump inhibitors, non-selective beta-blockers), and laboratory parameters (platelet, liver function test, prothrombin time, alpha-fetoprotein [AFP], anti-HBs). Statin users were propensity score matched (PSM) with non-users (1:2 ratio) for survival analysis of all outcomes.
Results:
Of 913 patients with HBsAg seroclearance (male: 613 [67.1%]; median age: 53.4 years [18.5-87.0]), 129 (14.1%) were statin users. During median follow-up of 7.7 years (up to 29.1 years), 64/833 (7.7%) developed cirrhosis, 25/905 (2.8%) developed HCC, 3/913 (0.3%) underwent transplantation, and 76/913 (8.3%) died. Statins were associated with lower cirrhosis/HCC risk (adjusted hazard ratio [aHR]: 0.44; 95% CI 0.20-0.96; aHR for every 1-year increase in use: 0.85; 95% CI 0.75-0.97). Statin users had no hepatic decompensation or liver-related death/transplantation (vs 18/778 [2.3%] and 18/784 [2.3%] cases in statin non-users, respectively). Statins were also associated with lower all-cause mortality risk (aHR: 0.21; 95% CI 0.08-0.53). PSM yields consistent results for beneficial effects of statins (log-rank p < 0.05 for all outcomes). Other factors for cirrhosis/HCC included increasing age (aHR: 1.06), diabetes (aHR: 2.03), higher creatinine (aHR: 1.008), GGT > 50U/L (aHR: 3.25), and AFP > 9 ng/mL (aHR: 10.14).
Conclusion:
Patients with HBsAg seroclearance have favorable long-term survival. However, liver-related adverse outcomes still develop, necessitating further investigations on beneficial effects of statins.
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