Division of Gastroenterology and Hepatology, Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Snyder Institute for Chronic Diseases, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Hepatol Commun. 2023 Feb 14;7(3):e0062. doi: 10.1097/HC9.0000000000000062. eCollection 2023 Mar 1.
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.
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.
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).
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.
慢性病毒性肝炎患者中常见抑郁症。我们评估了重型抑郁障碍(MDD)和抗抑郁药的使用对乙型肝炎病毒(HBV)和丙型肝炎病毒(HCV)患者生存的影响。
我们使用英国最大的医疗数据库——健康改善网络数据库,于 1986 年至 2017 年期间,确定了 1401 例 HBV 和 1635 例 HCV 患者的发病情况。我们的主要复合结局是失代偿性肝硬化或死亡的发生。在多变量 Cox 比例风险模型中评估 MDD 和每类抗抑郁药的情况。模型根据年龄、性别和临床合并症进行了调整。
HCV 患者的 MDD 患病率高于 HBV 患者(分别为 23.5%和 9.0%,p<0.001)。同样,HCV 患者使用抗抑郁药的可能性也高于 HBV 患者(59.6%和 27.1%,p>0.001)。MDD 不是失代偿性肝硬化无进展生存或死亡率的独立预测因素。然而,三环和四环抗抑郁药(TCAs)的使用与 HBV 和 HCV 队列的失代偿性肝硬化无进展生存率降低相关(调整后的 HR:1.80,95%CI,1.00-3.26 和 1.56,95%CI,1.13-2.14)。HBV 队列中的 TCAs 和 HCV 队列中的选择性 5-羟色胺再摄取抑制剂与总生存率降低相关(调整后的 HR:2.18,95%CI,1.16-4.10;1.48,95%CI,1.02-2.16)。
尽管在病毒性肝炎患者中很常见,但 MDD 并未影响 HBV 或 HCV 队列的疾病进展或生存。TCAs 的使用与失代偿性肝硬化无进展生存率降低相关。因此,应进一步研究其在病毒性肝炎患者中的应用。