Evidence map›Paper›PMID 22142332›Full record

Trial reportJournal of gastroenterology and hepatology2012

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

Maryam Alavi, Jason Grebely, Gail V Matthews, Kathy Petoumenos, Barbara Yeung, Carolyn Day, Andrew R Lloyd, Ingrid Van Beek, John M Kaldor, Margaret Hellard and 3 more

Open access · greenAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Journal of gastroenterology and hepatology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
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  11. Role of Inflammation in Suicide: From Mechanisms to Treatment.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2017
    Review
  12. Article
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  17. Review
  18. Evidence for a dysregulated immune system in the etiology of psychiatric disorders.Journal of neuroimmune pharmacology : the official journal of the Society on NeuroImmune Pharmacology · 2013
    Review
  19. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Maryam AlaviThe Kirby Institute for Infection and Immunity in Society, University of New South Wales, Sydney, Australia. msalehialavi@kirby.unsw.edu.au
Jason Grebely
Gail V Matthews
Kathy Petoumenos
Barbara Yeung
Carolyn Day
Andrew R Lloyd
Ingrid Van Beek
John M Kaldor
Margaret Hellard
Gregory J Dore
Paul S Haber
ATAHC Study Group
UNSW Sydney · AUUniversity of Sydney · AUBurnet Institute · AU

Funding

Treatment of recently acquired hepatitis C virus infectionR01DA015999 · NIDA · UNIVERSITY OF NEW SOUTH WALES · PI DORE, GREGORY JOHN · 2003 to 2014
$3.7M
NIDA NIH HHS R01 DA015999NIDA NIH HHS R01 DA15999-01
6 · The paper itself

Abstract

BACKGROUND AND

aimPegylated 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.

methodsParticipants with HCV received PEG-IFN-α-2a (180 µg/week) for 24 weeks; 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.

resultsOf 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).

conclusionsAlthough 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.

Indexed as

AdultAntiviral AgentsCoinfectionDepressionDrug Therapy, CombinationDrug UsersEmploymentFemaleHepatitis CHIV SeropositivityHumansInterferon-alphaLogistic ModelsMaleMental HealthPolyethylene GlycolsAntiviral AgentsInterferon-alphapeginterferon alfa-2aPolyethylene GlycolsRecombinant ProteinsRibavirin

Identifiers

PMID22142332
PMCPMC3331928
OpenAlexW1838542666

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.