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Impact of depression and antidepressant use on clinical outcomes of hepatitis B and C: a population-based study
Abdel Aziz Shaheen1,2, Gilaad G Kaplan1,2, Keith A Sharkey2,3,4
1Division of Gastroenterology and Hepatology, Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Insights
Major depressive disorder (MDD) did not impact survival in patients with hepatitis B (HBV) or C (HCV). However, tricyclic and tetracyclic antidepressants (TCAs) were linked to poorer survival outcomes in these viral hepatitis patient groups.
Area of Science:
- Hepatology
- Psychiatry
- Clinical Epidemiology
Background:
- Depression is a common comorbidity in patients with chronic viral hepatitis B (HBV) and hepatitis C (HCV).
- The impact of major depressive disorder (MDD) and antidepressant use on outcomes in these patient populations requires further investigation.
Purpose of the Study:
- To evaluate the association between major depressive disorder (MDD) and antidepressant use with survival in patients diagnosed with HBV and HCV.
- To determine if MDD or specific antidepressant classes influence the risk of decompensated cirrhosis or mortality in viral hepatitis patients.
Main Methods:
- Utilized The Health Improvement Network (THIN) database, a large UK medical database, to identify incident HBV (n=1401) and HCV (n=1635) cases between 1986 and 2017.
- Assessed MDD and antidepressant use (including TCAs and SSRIs) using multivariate Cox proportional hazards models, adjusting for clinical comorbidities, age, and sex.
- Primary composite outcome included the development of decompensated cirrhosis or death.
Main Results:
- MDD prevalence was significantly higher in HCV patients (23.5%) compared to HBV patients (9.0%).
- Antidepressant use was also more frequent in HCV patients (59.6%) versus HBV patients (27.1%).
- MDD was not an independent predictor of survival or decompensated cirrhosis. However, tricyclic and tetracyclic antidepressant (TCA) use was associated with poorer decompensated cirrhosis-free survival in both HBV and HCV cohorts. TCAs in HBV and selective serotonin reuptake inhibitors (SSRIs) in HCV were linked to poorer overall survival.
Conclusions:
- Despite its prevalence, MDD did not significantly affect disease progression or survival in HBV or HCV patients.
- Tricyclic and tetracyclic antidepressant (TCA) use was associated with adverse survival outcomes, specifically reduced decompensated cirrhosis-free survival.
- Further research is warranted to investigate the impact of TCA use on outcomes in patients with viral hepatitis.
Background:
Depression is common in patients with chronic viral hepatitis. We evaluated the impact of major depressive disorder (MDD) and antidepressant use on survival among patients with HBV and HCV.
Methods:
We used The Health Improvement Network database, the largest medical database in the UK, to identify incident HBV (n=1401) and HCV (n=1635) in patients between 1986 and 2017. Our primary composite outcome was the development of decompensated cirrhosis or death. MDD and each class of antidepressants were assessed in multivariate Cox proportional hazards models. Models were adjusted for age, sex, and clinical comorbidities.
Results:
The prevalence of MDD among HCV patients was higher compared with HBV patients (23.5% vs. 9.0%, p<0.001, respectively). Similarly, HCV patients were more likely to use antidepressants (59.6%) compared with HBV patients (27.1%), p>0.001. MDD was not an independent predictor for decompensated cirrhosis-free survival or mortality. However, the use of tricyclic and tetracyclic antidepressants (TCAs) was associated with poor decompensated cirrhosis-free survival in HBV and HCV cohorts (adjusted HR: 1.80, 95% CI, 1.00-3.26 and 1.56, 95% CI, 1.13-2.14, respectively). Both TCAs in the HBV cohort and selective serotonin reuptake inhibitors among the HCV cohort were associated with poor overall survival (adjusted HR: 2.18, 95% CI, 1.16-4.10; 1.48, 95% CI, 1.02-2.16, respectively).
Conclusions:
Although prevalent among viral hepatitis patients, MDD did not affect disease progression or survival in either HBV or HCV cohorts. TCA use was associated with poor decompensated cirrhosis-free survival. Therefore, its use should be further studied among viral hepatitis patients.
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