Evidence map›Paper›PMID 25042607›Full record

ArticleHepatology (Baltimore, Md.)2014

Phylogenetic clustering of hepatitis C virus among people who inject drugs in Vancouver, Canada.

B Jacka, T Applegate, M Krajden, A Olmstead, P R Harrigan, Bdl Marshall, K DeBeck, M-J Milloy, F Lamoury, O G Pybus and 10 more

Abstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
–field-weighted citation impact
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

43 citing papers in PubMed.

  1. Observational
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
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  8. Article
  9. Article
  10. Article
  11. Identification of Genetically Related HCV Infections Among Self-Described Injecting Partnerships.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2022
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Correlates of hepatitis C viral clustering among people who inject drugs in Baltimore.Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2020
    Article
  20. Article
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

20 authors.

B JackaViral Hepatitis Clinical Research Program, The Kirby Institute, UNSW Australia, Sydney NSW, Australia.
T ApplegateViral Hepatitis Clinical Research Program, The Kirby Institute, UNSW Australia, Sydney NSW, Australia.
M KrajdenBC Centre for Disease Control, Vancouver BC.
A OlmsteadBC Centre for Disease Control, Vancouver BC.
P R HarriganBC Centre for Excellence in HIV/AIDS, St Paul's Hospital, Vancouver BC.
Bdl MarshallDepartment of Epidemiology, Brown University, Providence, RI, USA.
K DeBeckBC Centre for Excellence in HIV/AIDS, St Paul's Hospital, Vancouver BC.
M-J MilloyBC Centre for Excellence in HIV/AIDS, St Paul's Hospital, Vancouver BC.
F LamouryViral Hepatitis Clinical Research Program, The Kirby Institute, UNSW Australia, Sydney NSW, Australia.
O G PybusDepartment of Zoology, University of Oxford.
V D LimaBC Centre for Excellence in HIV/AIDS, St Paul's Hospital, Vancouver BC.
G MagiorkinisDepartment of Zoology, University of Oxford.
V MontoyaBC Centre for Disease Control, Vancouver BC.
J MontanerBC Centre for Excellence in HIV/AIDS, St Paul's Hospital, Vancouver BC.
J JoyBC Centre for Excellence in HIV/AIDS, St Paul's Hospital, Vancouver BC.
C WoodsBC Centre for Excellence in HIV/AIDS, St Paul's Hospital, Vancouver BC.
S DobrerBC Centre for Excellence in HIV/AIDS, St Paul's Hospital, Vancouver BC.
G J DoreViral Hepatitis Clinical Research Program, The Kirby Institute, UNSW Australia, Sydney NSW, Australia.
A F Poon *BC Centre for Excellence in HIV/AIDS, St Paul's Hospital, Vancouver BC.
J Grebely *Viral Hepatitis Clinical Research Program, The Kirby Institute, UNSW Australia, Sydney NSW, Australia.

Funding

SYRINGE ACCESS AND RISK FACTORS ON HIV TRANSMISSIONR01DA011591 · NIDA · UNIVERSITY OF BRITISH COLUMBIA · PI KERR, THOMAS · 1998 to 2014
$5.9M
Seek and Treat for Optimal Outcomes and Prevention in HIV & AIDS in IDUDP1DA026182 · NIDA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI MONTANER, JULIO SERGIO GONZALEZ · 2008 to 2013
$3.9M
Modeling different strategies to reduce the public health impact of the HCV/HIV eR03DA033851 · NIDA · UNIVERSITY OF BRITISH COLUMBIA · PI LIMA, VIVIANE DIAS · 2012 to 2013
$55k
CIHR 125948-1CIHR 129971-1CIHR HES-115697CIHR HHP-67262CIHR MOP-125948CIHR RAA-79918Medical Research Council MR/K010565/1NIDA NIH HHS DP1 DA026182NIDA NIH HHS R01 DA011591NIDA NIH HHS R01DA011591NIDA NIH HHS R03 DA033851NIDA NIH HHS R03DA033851-01
6 · The paper itself

Abstract

unlabelledLittle is known about factors associated with hepatitis C virus (HCV) transmission among people who inject drugs (PWID). Phylogenetic clustering and associated factors were evaluated among PWID in Vancouver, Canada. Data were derived from the Vancouver Injection Drug Users Study. Participants who were HCV antibody-positive at enrolment and those with HCV antibody seroconversion during follow-up (1996 to 2012) were tested for HCV RNA and sequenced (Core-E2 region). Phylogenetic trees were inferred using maximum likelihood analysis and clusters were identified using ClusterPicker (90% bootstrap threshold, 0.05 genetic distance threshold). Factors associated with clustering were assessed using logistic regression. Among 655 eligible participants, HCV genotype prevalence was: G1a: 48% (n=313), G1b: 6% (n=41), G2a: 3% (n=20), G2b: 7% (n=46), G3a: 33% (n=213), G4a: <1% (n=4), G6a: 1% (n=8), G6e: <1% (n=1), and unclassifiable: 1% (n=9). The mean age was 36 years, 162 (25%) were female, and 164 (25%) were HIV+. Among 501 participants with HCV G1a and G3a, 31% (n=156) were in a pair/cluster. Factors independently associated with phylogenetic clustering included: age <40 (versus age≥40, adjusted odds ratio [AOR]=1.64; 95% confidence interval [CI] 1.03, 2.63), human immunodeficiency virus (HIV) infection (AOR=1.82; 95% CI 1.18, 2.81), HCV seroconversion (AOR=3.05; 95% CI 1.40, 6.66), and recent syringe borrowing (AOR 1.59; 95% CI 1.07, 2.36).

conclusionIn this sample of PWID, one-third demonstrated phylogenetic clustering. Factors independently associated with phylogenetic clustering included younger age, recent HCV seroconversion, prevalent HIV infection, and recent syringe borrowing. Strategies to enhance the delivery of prevention and/or treatment strategies to those with HIV and recent HCV seroconversion should be explored, given an increased likelihood of HCV transmission in these subpopulations.

Indexed as

Drug UsersPhylogenyAdultBritish ColumbiaCluster AnalysisFemaleHepacivirusHepatitis CHumansMaleProspective Studies

Identifiers

PMID25042607
PMCPMC4211947

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Registered trials

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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.