Antidepressants are effective in treating interferon-α/ribavirin (IFN-α/RBV)-associated depression during or after treatment of chronic hepatitis C (CHC). Whether antidepressant prophylaxis is necessary in this population remains under debate.
Comprehensive searches were performed in Medline, Embase, Cochrane Controlled Trials Register and PubMed. Reference lists were searched manually. The methodology was in accordance with the 2009 PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analysis) Statement.
We identified six randomized, double-blind, placebo-controlled trials involving 522 CHC patients treated with pegylated (PEG)-IFN-α plus RBV. The antidepressants used were escitalopram, citalopram, and paroxetine, which are selective serotonin reuptake inhibitors (SSRIs). The rates of depression (17.9% vs. 31.0%, P = 0.0005), and rescue therapy (27.4% vs. 42.7%, P<0.0001) in the SSRI group were significantly lower than those in the placebo group. The rate of sustained virological response (SVR) (56.8% vs. 50.0%, P = 0.60) and drug discontinuation (18.7% vs. 21.1%, P = 0.63) in the SSRI group did not differ significantly to those in the placebo group. In terms of safety, the incidence of muscle and joint pain (40.8% vs. 52.4%, P = 0.03) and respiratory problems (29.3% vs. 40.1%, P = 0.03) were lower, but the incidence of dizziness was significantly higher (22.3% vs. 10.2%, P = 0.001) in the SSRI group.
Citation: Hou X-J, Xu J-H, Wang J, Yu Y-Y (2013) Can Antidepressants Prevent Pegylated Interferon-α/Ribavirin-Associated Depression in Patients with Chronic Hepatitis C: Meta-Analysis of Randomized, Double-Blind, Placebo-Controlled Trials? PLoS ONE 8(10): e76799. https://doi.org/10.1371/journal.pone.0076799
Editor: Ming-Lung Yu, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Taiwan
Received: April 17, 2013; Accepted: August 28, 2013; Published: October 30, 2013
Copyright: © 2013 Hou et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: The authors have no support or funding to report.
Competing interests: The authors have declared that no competing interests exist.
Globally, hepatitis C virus (HCV) has become one of the leading causes of chronic liver diseases and affects >170 million people , . The severity of the disease associated with HCV infection varies from asymptomatic chronic infection to all types of end-stage liver diseases, including cirrhosis and hepatocellular carcinoma . To date, combination of pegylated interferon-α (PEG-IFN-α) plus ribavirin (RBV) is considered to be the most effective treatment for chronic hepatitis C (CHC). It is recommended in the American Association for the Study of Liver Diseases (AASLD) practical guidelines .
However, IFN-α-based therapy is associated with an approximately 70% incidence of mild to moderate depressive syndromes – and 20–40% incidence of major depression in HCV patients . IFN-associated depression can lead to deterioration in quality of life, and has become a major contribution to treatment withdrawal, non-compliance, dose reduction of IFN/RBV, and even attempted suicide –; all of which can result in treatment failure –. Furthermore, depressive symptoms are closely related to poor virological response , . Therefore, there is urgency in preventing the occurrence of depression in IFN-α-based therapy.
Although some studies have reported that antidepressants are effective in treating IFN-α/RBV-associated depression during or after treatment of CHC –, whether antidepressant prophylaxis is necessary in this population remains a subject for debate –.
Consequently, the aim of this meta-analysis was to evaluate the efficacy and safety of pretreatment with antidepressants to prevent IFN-α/RBV-associated depression in patients with CHC treated with antiviral therapy in randomized, double-blind, placebo-controlled trials.
Materials and Methods
Two authors performed a literature search on Medline (1966 to March 2013), PubMed (updated to March 2013), Embase (1980 to March 2013), and Cochrane Controlled Trials Register (Cochrane Library Issue 1, 2013) using the keywords “hepatitis C AND interferon AND depression”. A manual search of publications and manual review of major journals in internal medicine, gastroenterology, hepatology, and infectious diseases (2000–2012) were also performed. This meta-analysis was conducted and reported according to the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analysis) Statement issued in 2009 .
Inclusion criteria were: (1) study population with CHC; (2) antiviral regime was IFN-<alpha>/RBV combination therapy; (3) studies that reported data for outcomes at the end of treatment and follow-up period; (4) studies with full text; and (5) English studies. Exclusion criteria were: (1) non-randomized controlled trials (RCTs); (2) non-prophylaxis studies with pretreatment with antidepressants before antiviral therapy; (3) studies about human immunodeficiency virus, hepatitis B virus or other virus co-infections; and (4) studies about organ transplantation.
Two investigators independently evaluated each study, each of whom was blinded to the other. Any discrepancy was resolved through discussion. Extracted information included study characteristics (first author, study location, and year); patient baseline characteristics (sex, risk factors, baseline HCV RNA, HCV genotype, body mass index, and percentage with fibrosis and cirrhosis); and antidepressant and antiviral regimens. Outcomes included: total number of patients; number of patients with IFN-associated depression at the end of treatment; number of patients with sustained virological response (SVR) at the end of follow-up (defined as undetectable HCV RNA at the end of follow-up); total number of patients with treatment discontinuation; number of patients with serious adverse events; number of patients with dose reduction due to adverse events; and number of patients who received antidepressant rescue treatment.
Quality of methodology
Assessment of the methodological quality of the trials was based on the Jadad composite scale , which evaluated randomization, concealment and reporting of patient withdrawal and dropout rates, with ≥3 scores defined as high quality, and ≤2 as low quality. Heterogeneity was assessed for each analysis. The methodological quality was assessed independently by two of the authors.
The statistical analyses were conducted and Forest plots were generated using RevMan 5.2.3 (Nordic Cochrane Center, Rigshospitalet, Copenhagen, Denmark). The primary endpoints were the rate of incidence of depression and the rate of SVR. The secondary endpoints were the rate of drug discontinuation or withdrawal, rate of antidepressant rescue treatment, and the rate of adverse events. For the calculation of risk ratios (RRs), patients assigned to prophylactic antidepressant treatment were compared with those assigned to placebo in the same trial. The RRs were calculated along with their respective 95% confidence intervals (CIs) and presented for each individual study. Statistical heterogeneity between trials was evaluated by the χ2 and I2 tests, with significance being set at P<0.10. In the absence of significant heterogeneity (P>0.10), the fixed-effect method was used to combine the results. When heterogeneity was confirmed (P≤0.10), the random-effect method was used, and sensitivity analyses and meta-regressions were performed with study characteristics to evaluate potential sources of heterogeneity. Stratified analyses were performed using the variables found to be statistically significant in the meta-regressions. Any potential publication bias was evaluated by inspecting funnel plots and the Begg–Mazumdar test .
Of the 871 articles found after initial searching, six studies involving 522 patients met the inclusion criteria –. A flow chart summarizing the search and screening process is presented in Figure 1. Placebo-controlled design and intention-to-treat analysis were conducted in all trials. The antidepressants used in the present meta-analysis were escitalopram, citalopram, and paroxetine, all of which are selective serotonin reuptake inhibitors (SSRIs). The antiviral therapies administrated in all studies were PEG-IFN-α/RBV, with exception of IFN-α/RBV in some patients in two studies. The baseline patient characteristics and depression scoring system are listed in Table 1. Study design and antidepressant and antiviral regimens are listed in Table 2.
Rate of depression
All six trials provided data about the rate of PEG-IFN-α/RBV-associated depression. The SSRI group included 252 patients with a rate of depression of 17.9%, while the placebo group included 261 patients with a rate of depression of 31.0%. The test for heterogeneity of the data obtained a P value of 0.27, thus the hypothesis of homogeneity was achieved. An estimated RR of 0.58 (95% CI: 0.43–0.79) was obtained after the data were pooled, and a significant effect on the rate of depression was found for the prophylaxis of SSRIs to prevent PEG-IFN-α/RBV-associated depression in patients with CHC (P = 0.0005) (Figure 2). The subgroup analyses of different SSRIs for the rate of depression are shown in Table 3.
Rate of SVR
Four trials reported data on the effect of antidepressants on SVR. The SSRI group included 176 patients with a rate of SVR of 56.8%, while the placebo group included 184 patients with a rate of SVR of 50.0%. The test for the heterogeneity of the data obtained a P value of 0.08, thus the random model was used. An estimated RR of 1.10 (95% CI: 0.78–1.55) was obtained after the data were pooled. Antidepressant prophylaxis had no significant effect on the rate of SVR in patients with CHC (P = 0.60) (Figure 3). The subgroup analyses of different SSRIs for the rate of SVR are shown in Table 3.
Rate of drug discontinuation
All of the trials reported data on drug discontinuation. The SSRI group included 257 patients with a rate of discontinuation of 18.7%, while the placebo group included 265 patients with a rate of discontinuation of 21.1%. The test for heterogeneity of the data obtained a P value of 0.27, thus the hypothesis of homogeneity was achieved. An estimated RR of 0.92 (95% CI: 0.66–1.29) was obtained after the data were pooled. Antidepressant prophylaxis had no significant effect on the rate of discontinuation in patients with CHC (P = 0.63) (Figure 4). The subgroup analyses of different SSRIs for the rate of discontinuation are shown in Table 3.
Rate of rescue therapy
Four trials reported data on the number of patients receiving rescue therapy. The SSRI group included 215 patients with a rate of rescue therapy of 27.4%, while the placebo group included 213 patients with a rate of rescue therapy of 42.7%. The test for heterogeneity of the data obtained a P value of 0.13, thus the hypothesis of homogeneity was achieved. An estimated RR of 0.63 (95% CI: 0.51–0.78) was obtained after the data were pooled, and a significant effect on the rate of rescue therapy was found (P<0.0001) (Figure 5). The subgroup analyses of different SSRIs for the rate of rescue therapy are shown in Table 3.
Data for adverse events were extracted from three trials and subjected to meta-analysis (Table 4). The rate of muscle and joint pain in the SSRI group was significantly lower than that in the placebo group (40.8% vs. 52.4%, P = 0.03). The rate of respiratory problems in the SSRI group was significantly lower than that in the placebo group (29.3% vs. 40.1%, P = 0.03) (Figure 6). The rate of respiratory problems in the escitalopram group was also significantly lower than that in the placebo group (29.5% vs. 44.2%, P = 0.008) (Table 4). However, the rate of dizziness in the SSRI group was significantly higher than that in the placebo group (22.3% vs. 10.2%, P = 0.001) (Figure 6). The rate of dizziness in the escitalopram group was also significantly higher than that in the placebo group (19.2% vs. 9.7%, P = 0.02) (Table 4).
We performed this meta-analysis of randomized double-blind placebo-controlled clinical trials to evaluate the efficacy and safety of prophylactic antidepressants to prevent PEG-IFN-α/RBV-associated depression in patients with CHC. The results reveal that preemptive and concomitant therapy with SSRIs can significantly reduce the incidence of PEG-IFN-α/RBV-associated depression in patients with CHC. SSRI interventions were safe, did not negatively decrease SVR, and did not influence the rate of drug discontinuation or withdrawal.
Interferon-α/RBV-associated depression is characteristic of a serotonergic deficiency and changes in the serotonin signaling pathway, which requires the prophylactic administration of SSRIs , because these drugs increase serotonin and have been widely used over the past decade, with a good safety profile .
The pooled rate of depression in the placebo group was 31.0%, which fell within the 20–40% incidence of depression in patients treated with IFN-α/RBV . Compared with placebo, prophylactic antidepressants can significantly reduce the incidence of PEG-IFN-α/RBV-associated depression, by up to 18.7% in CHC patients without a history of severe mental disease. Although standard INF-α was used in some CHC patients in two studies , , the results from the other four trials showed that antidepressants markedly decreased the incidence of depression to 17.2% during PEG-IFN-α-based antiviral therapy. Furthermore, both current types of PEG-IFN-α, that is, PEG-IFN-α2a and 2b, were administrated in all six trials, so the type of IFN-α may be ignored when prophylactic SSRIs are used in patients with CHC. Escitalopram and paroxetine share the same mechanism of action to treat depression, although the former is superior to the latter for prophylactic intervention according to the present study. Escitalopram was developed after citalopram and is considered safer and more effective for treating major depression. However, a previous meta-analysis showed that escitalopram was not superior to citalopram in short-to-medium term treatment of major depressive disorder . The rate of depression was 10.5% when citalopram was used , which was lower than 17.9%—the pooled rate of depression in three trials when escitalopram was used , , . However, the sample size in the trial on citalopram was only 39 patients, which was 10% of the pooled sample in the three trials of escitalopram. Clinically, clinicians should pay more attention to the results of meta-analyses.
With respect to the effect of SSRIs on the SVR, the results varied among the trials, although the trials were of similar design , , , . The pooled SVR rate in the setting of prophylactic SSRIs did not differ significantly compared with that in the placebo group. Subgroup analysis also reached a similar conclusion. Consequently, prophylactic SSRIs have little effect on the SVR in patients with CHC when they are treated with antiviral therapy. However, we suggest that escitalopram should be used because of the higher SVR rate and its increased use for intervention in depression.
IFN-α/RBV-associated depression was an important reason for discontinuing antiviral therapy , . Consequently, successful treatment of CHC needs prevention of depression. The pooled rate of drug discontinuation differed significantly between the SSRI and placebo groups after subgroup analyses, which was consistent with the results from each trial individually. These results suggest that prophylactic SSRIs have little effect on drug discontinuation during treatment of CHC with the currently available antiviral therapy.
The lower rates of rescue therapy, muscle and joint pain and respiratory problems in the SSRI group indicated the better safety and tolerability of SSRIs. These results suggest that prophylactic SSRIs reduce the occurrence of these two adverse events associated with PEG-IFN-α/RBV combination therapy in patients with CHC. However, the pooled rate of dizziness was higher in the SSRI group than the placebo group, which was consistent with the results of each separate trial. This reminds clinicians to pay more attention to the occurrence of this adverse event when prophylactic SSRIs are administrated to patients with CHC. Therefore, prophylactic SSRIs did not worsen most adverse events apart from dizziness. Moreover, adverse events (e.g. diarrhea, headache, and sleep disturbance) were not increased as a result of concurrent administration of antiviral therapy and SSRIs. Although it was reported that citalopram could be safely used during IFN treatment in patients with CHC , there were risks of using SSRIs during IFN treatment, because CHC may alter the pharmacokinetics of SSRIs. Therefore, SSRI dose may require adjustment to optimize the treatment .
We need to emphasize that according to our clinical experience and inclusion criteria, the optimal candidates for SSRI prophylaxis are CHC patients with concurrent subsyndromal depression symptoms (such as insomnia and anxiety) or a history of past major depressive disorders and eligibility for PEG-IFN-α/RBV treatment.
There were several limitations to our study. First, only six eligible RCTs were included, and we were limited by data availability. Second, sample sizes in most of the trials were small and included <50 subjects. Third, the possibility of omission of unpublished or ongoing studies still exist, although publication bias was not found according to the funnel plots and the Begg–Mazumdar test. Fourth, possible variation in the definition of depression and severity of depression were present in the studies included in our analysis, although the criteria for diagnosis and severity of depression were similar in all studies. These defects may weaken our results. Further analysis of increased numbers of multicenter RCTs with larger sample sizes are warranted to evaluate comprehensively the true value of prophylactic SSRIs to prevent PEG-IFN-α/RBV-associated depression during antiviral therapy in patients with CHC.
Despite these limitations, our meta-analysis of double-blind, placebo-controlled RCTs shows that prophylactic SSRIs can significantly reduce the incidence of PEG-IFN-α/RBV-associated depression in patients with CHC, with good safety and tolerability and without reduction of SVR.
PRISMA 2009 Flow Diagram.
PRISMA 2009 Checklist.
Conceived and designed the experiments: XJH YYY. Performed the experiments: XJH JHX. Analyzed the data: XJH JW. Contributed reagents/materials/analysis tools: JHX JW. Wrote the paper: XJH YYY.
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