TY - JOUR
T1 - Effect of pegylated interferon-α-2a treatment on mental health during recent hepatitis C virus infection
AU - Alavi, Maryam
AU - Grebely, Jason
AU - Matthews, Gail V.
AU - Petoumenos, Kathy
AU - Yeung, Barbara
AU - Day, Carolyn
AU - Lloyd, Andrew R.
AU - Van Beek, Ingrid
AU - Kaldor, John M.
AU - Hellard, Margaret
AU - Dore, Gregory J.
AU - Haber, Paul S.
AU - Amin, Janaki
AU - Doab, Anna
AU - Carroll, Therese
AU - Ffrench, Rose
AU - Flynn, Jacqueline
AU - Goy, Kylie
AU - Nguyen, Oanh
AU - von Bibra, Sally
AU - White, Peter
AU - Li, Hui
AU - Oon, Alieen
AU - Cameron, Barbara
AU - Rawlinson, William
AU - Dolan, Kate
AU - Jacka, Brendan
AU - Pan, Yong
AU - Haber, Paul
AU - McCaughan, Geoff
AU - Madden, Annie
AU - Farrell, Geoff
AU - Crofts, Nick
AU - Sievert, William
AU - Baker, David
AU - Desmond, Paul
AU - Hellard, Margaret
AU - Shaw, David
AU - Sasadeusz, Joe
AU - Crawford, Darrell
AU - Phung, Nghi
AU - George, Jacob
AU - Bloch, Mark
AU - Hughes, Brian
AU - Mollison, Lindsay
AU - Roberts, Stuart
AU - ATAHC Study Group
PY - 2012/5/1
Y1 - 2012/5/1
N2 - 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-α-2a (180μg/week) for 24weeks; HCV/HIV received PEG-IFN with ribavirin. Depression was assessed using the Mini-International 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.
AB - 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-α-2a (180μg/week) for 24weeks; HCV/HIV received PEG-IFN with ribavirin. Depression was assessed using the Mini-International 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.
KW - Anxiety
KW - Depression
KW - Hepatitis C virus
KW - Injecting drug users
KW - Psychiatric
UR - http://www.scopus.com/inward/record.url?scp=84860233144&partnerID=8YFLogxK
U2 - 10.1111/j.1440-1746.2011.07035.x
DO - 10.1111/j.1440-1746.2011.07035.x
M3 - Article
C2 - 22142332
AN - SCOPUS:84860233144
SN - 0815-9319
VL - 27
SP - 957
EP - 965
JO - Journal of Gastroenterology and Hepatology (Australia)
JF - Journal of Gastroenterology and Hepatology (Australia)
IS - 5
ER -