Effect of pegylated interferon-α-2a treatment on mental health during recent hepatitis C virus infection

被引:42
作者
Alavi, Maryam [1 ]
Grebely, Jason [1 ]
Matthews, Gail V. [1 ]
Petoumenos, Kathy [1 ]
Yeung, Barbara [1 ]
Day, Carolyn [3 ]
Lloyd, Andrew R. [2 ]
Van Beek, Ingrid [5 ]
Kaldor, John M. [1 ]
Hellard, Margaret [6 ]
Dore, Gregory J. [1 ]
Haber, Paul S. [2 ,4 ]
机构
[1] Univ New S Wales, Kirby Inst Infect & Immun Soc, Sydney, NSW, Australia
[2] Univ New S Wales, Sch Med Sci, Sydney, NSW, Australia
[3] Univ Sydney, Drug Hlth Serv, Cent Clin Sch C39, Sydney, NSW 2006, Australia
[4] Univ Sydney, Cent Clin Sch, Sydney, NSW 2006, Australia
[5] Kirketon Rd Ctr, Sydney, NSW, Australia
[6] Burnet Inst, Melbourne, Vic, Australia
基金
英国医学研究理事会; 美国国家卫生研究院;
关键词
anxiety; depression; hepatitis C virus; injecting drug users; psychiatric; INJECTING DRUG-USERS; INDUCED DEPRESSION; RIBAVIRIN THERAPY; PLUS RIBAVIRIN; DSM-IV; ALPHA; SYMPTOMS; PEGINTERFERON; ELIGIBILITY; COMORBIDITY;
D O I
10.1111/j.1440-1746.2011.07035.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and Aim: Pegylated interferon (PEG-IFN) treatment for hepatitis C virus (HCV) infection has neuropsychiatric side effects. Data on the effect of HCV treatment on mental health among injecting drug users (IDUs) are limited. We assessed mental health during treatment of recently acquired HCV, within a predominantly IDU population. Methods: Participants with HCV received PEG-IFN-a-2a (180 mg/ week) for 24 weeks; HCV/ HIV received PEG-IFN with ribavirin. Depression was assessed using the MiniInternational Neuropsychiatric Interview (MINI). Logistic regression was used to identify factors associated with depression at enrolment and during treatment. Also, the effect of depression prior to and during treatment on sustained virological response (SVR) was assessed. Results: Of 163 participants, 111 received treatment (HCV, n = 74; HCV/ HIV, n = 37), with 76% ever reporting IDU. At enrolment, 16% had depression (n = 25). In adjusted analysis, depression at enrolment occurred less often in participants full-/part-time employed (adjusted odds ratio [AOR] 0.23; 95% confidence interval [CI]: 0.06, 0.82, P = 0.023) and more often in recent IDUs (AOR 3.04; 95% CI: 1.19, 7.72, P = 0.019). During treatment, 35% (n = 31) developed new-onset depression. In adjusted analysis, poorer social functioning (higher score) was associated with new-onset depression (score <= 9 vs score >= 17; OR 5.69; 95% CI: 1.61, 20.14, P = 0.007). SVR was similar among participants with and without depression at enrolment (60% vs 61%, P = 0.951) and in those with and without new-onset depression (74% vs 63%, P = 0.293). Conclusions: Although depression at enrolment and during treatment was common among participants with recent HCV, neither influenced SVR. Participants with poor social functioning may be most at risk of developing depression during HCV therapy.
引用
收藏
页码:957 / 965
页数:9
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