Evidence map›Paper›PMID 29020200›Full record

Observational studyClinical infectious diseases : an official publication of the Infectious Diseases Society of America2018

The Effect of Female Sex on Hepatitis C Incidence Among People Who Inject Drugs: Results From the International Multicohort InC3 Collaborative.

Aryan Esmaeili, Ali Mirzazadeh, Meghan D Morris, Behzad Hajarizadeh, Henry S Sacks, Lisa Maher, Jason Grebely, Arthur Y Kim, Georg Lauer, Andrea L Cox and 9 more

Open access · bronzeAbstract readObservational Study
In one paragraph

Observational study in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
2.2field-weighted citation impact, top 12% 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

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 33 citations in OpenAlex.

  1. Pooled it
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  14. Review
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  16. Article
  17. Sex Discrepancies in the Protective Effect of Opioid Agonist Therapy on Incident Hepatitis C Infection.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2020
    Article
  18. Article
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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

19 authors at 9 institutions in 4 countries.

Aryan EsmaeiliThomas C. Chalmers Clinical Trials Unit, Icahn School of Medicine at Mount Sinai, New York, New York.
Ali MirzazadehDepartment of Epidemiology and Biostatistics, University of California, San Francisco.
Meghan D MorrisDepartment of Epidemiology and Biostatistics, University of California, San Francisco.
Behzad HajarizadehKirby Institute, University of New South Wales, Sydney, Australia.
Henry S SacksThomas C. Chalmers Clinical Trials Unit, Icahn School of Medicine at Mount Sinai, New York, New York.
Lisa MaherKirby Institute, University of New South Wales, Sydney, Australia.
Jason GrebelyKirby Institute, University of New South Wales, Sydney, Australia.
Arthur Y KimHarvard Medical School, Boston, Massachusetts.
Georg LauerHarvard Medical School, Boston, Massachusetts.
Andrea L CoxDepartment of Medicine, Johns Hopkins University, Baltimore, Maryland.
Margaret HellardBurnet Institute, Melbourne, Victoria, Australia.
Paul DietzeBurnet Institute, Melbourne, Victoria, Australia.
Julie BruneauCentre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Université de Montréal, Québec, Canada.
Naglaa H ShoukryCentre de Recherche du Centre Hospitalier de l'Université de Montréal (CRCHUM), Université de Montréal, Québec, Canada.
Gregory J DoreKirby Institute, University of New South Wales, Sydney, Australia.
Andrew R LloydSchool of Medical Sciences, University of New South Wales, Sydney, Australia.
Maria PrinsThe Public Health Service of Amsterdam (GGD Amsterdam), The Netherlands.
Kimberly PageDivision of Epidemiology, Biostatistics and Preventive Medicine, Department of Internal Medicine, University of New Mexico Health Sciences Center, Albuquerque.
InC3 Collaborative
UNSW Sydney · AUBurnet Institute · AUCentre Hospitalier de l’Université de Montréal · CAHarvard University · USIcahn School of Medicine at Mount Sinai · USUniversity of California, San Francisco · USGGD Amsterdam · NLJohns Hopkins University · USUniversity of New Mexico · US

Funding

Tracking and EvaluationU54GM104944 · NIGMS · UNIVERSITY OF NEVADA LAS VEGAS · PI MARCHAND, GWEN · 2013 to 2023
$39.6M
UNM HSC Clinical and Translational Science CenterUL1TR001449 · NCATS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI CAMPEN, MATTHEW J, PANDHI, NANCY · 2015 to 2024
$36.9M
Acute Hepatitis C Infection in Young InjectorsR01DA016017 · NIDA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI PAGE, KIMBERLY · 2002 to 2018
$14.0M
The role of NK cells during acute HCV infection and antiviral therapyU19AI066345 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI LAUER, GEORG MICHAEL · 2005 to 2014
$8.5M
Scientific CoreU19AI088791 · NIAID · JOHNS HOPKINS UNIVERSITY · PI COX, ANDREA L · 2010 to 2020
$8.2M
International Collaborative of prospective studies of HIV and Hepatitis in IDUR01DA031056 · NIDA · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI PAGE, KIMBERLY · 2011 to 2015
$2.2M
NCATS NIH HHS UL1 TR001449NIAID NIH HHS U19 AI066345NIAID NIH HHS U19 AI088791NIDA NIH HHS R01 DA016017NIDA NIH HHS R01 DA031056NIGMS NIH HHS U54 GM104944
6 · The paper itself

Abstract

Background: The objective of this study was to assess differences in hepatitis C virus (HCV) incidence by sex in people who inject drugs (PWID), using a large international multicohort set of pooled biological and behavioral data from prospective observational studies of incident human immunodeficiency virus (HIV) and HCV infections in high-risk cohorts (the InC3 Collaborative). Methods: HCV infection date was estimated based on a hierarchy of successive serological (anti-HCV), virological (HCV RNA), and clinical (symptoms and/or liver function tests) data. We used a Cox proportional hazards model to calculate the crude and adjusted female to male (F:M) hazard ratio (HR) for HCV incidence using biological sex as the main exposure. Results: A total of 1868 PWID were observed over 3994 person-years of observation (PYO). Unadjusted F:M HR was 1.38 (95% confidence interval [CI], 1.15-1.65) and remained significant after adjusting for behavioral and demographic risk factors (1.39 [95% CI, 1.12-1.72]). Although syringe and equipment sharing were associated with the highest HCV incidence rate in women (41.62 and 36.83 PYO, respectively), we found no sex differences attributed to these risk factors. Conclusions: Our findings indicate that women who inject drugs may be at greater risk of HCV acquisition than men, independent of demographic characteristics and risk behaviors. Multiple factors, including biological (hormonal), social network, and differential access to prevention services, may contribute to increased HCV susceptibility in women who inject drugs.

Indexed as

Sex FactorsAdultFemaleHepatitis CHumansIncidenceMaleProspective StudiesRisk FactorsSubstance Abuse, Intravenoushepatitis C virusincidencepeople who inject drugssexsurvival analysis

Identifiers

PMID29020200
PMCPMC5850635
OpenAlexW2753283012

What OpenQuestion holds

Textmetadata
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.