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Antiviral Therapy Reduces Dyslipidemia and Cardiovascular Risk in Chronic Hepatitis B: TDF as the Most Effective
Hyuk Kim1, Jae-Young Kim2, Hyun Bin Choi1
1Department of Internal Medicine, Division of Gastroenterology and Hepatology, Soonchunhyang University Bucheon Hospital, Bucheon-si, Korea.
Insights
Antiviral therapy for chronic hepatitis B (CHB) significantly reduces the risk of dyslipidemia and major adverse cardiovascular events (MACE). Tenofovir disoproxil fumarate (TDF) offers the most substantial protection, highlighting extrahepatic benefits beyond viral suppression.
Area of Science:
- Hepatology
- Cardiology
- Metabolic Syndrome
Background:
- Chronic hepatitis B (CHB) necessitates long-term antiviral treatment.
- The impact of CHB antiviral therapy on metabolic and cardiovascular health is not fully understood.
Purpose of the Study:
- To investigate the effects of antiviral therapy on dyslipidemia and major adverse cardiovascular events (MACE) in CHB patients.
- To assess the specific benefits of tenofovir disoproxil fumarate (TDF).
Main Methods:
- Nationwide retrospective cohort study using Korean Health Insurance Review and Assessment data.
- Propensity score matching of 48,606 treated CHB patients with untreated controls.
- Analysis of incidence rates and hazard ratios for dyslipidemia and MACE.
Main Results:
- Antiviral therapy significantly lowered incidence rates of dyslipidemia (IRR: 0.80) and MACE (IRR: 0.78).
- Tenofovir disoproxil fumarate (TDF) demonstrated the strongest protective effects (aHR: 0.52 for dyslipidemia, 0.58 for MACE).
- Protective effects were more pronounced in non-diabetic patients.
Conclusions:
- Antiviral therapy for CHB offers significant extrahepatic benefits, including reduced risk of dyslipidemia and MACE.
- TDF is particularly effective in mitigating these risks.
- These findings support the use of antiviral therapy in comprehensive long-term CHB management.
Abstract:
Chronic hepatitis B (CHB) requires long-term antiviral therapy, but its broader effects on metabolic and cardiovascular outcomes remain underexplored. This nationwide retrospective cohort study aimed to evaluate the impact of antiviral therapy on dyslipidemia and major adverse cardiovascular events (MACE) in CHB patients. Using the Korean Health Insurance Review and Assessment database, we identified 441 191 patients, of whom 48 606 received antiviral treatment and were matched 1:1 with untreated controls by propensity score. Antiviral therapy was associated with significantly lower incidence rates of both dyslipidemia (14.63 vs. 18.20 per 100 000 person-years; IRR: 0.80, 95% CI: 0.76-0.85) and MACE (2.15 vs. 3.08 per 100 000 person-years; IRR: 0.78, 95% CI: 0.67-0.91). Tenofovir disoproxil fumarate (TDF) showed the strongest protective effects against both outcomes, with adjusted hazard ratios of 0.52 for dyslipidemia and 0.58 for MACE. Stratified analysis revealed that the protective effects of antiviral therapy against dyslipidemia and MACE were primarily observed in nondiabetic patients, while only a nonsignificant trend toward risk reduction was noted in diabetic patients. These findings suggest that antiviral therapy, particularly TDF, provides extrahepatic benefits, supporting its role in the long-term management of CHB beyond virologic suppression.
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