Incidence of HIV and hepatitis C virus among people who inject drugs, and associations with age and sex or gender: a global systematic review and meta-analysis

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22 Scopus citations

Abstract

Background: Measuring the incidence of HIV and hepatitis C virus (HCV) infection among people who inject drugs (PWID) is key to track progress towards elimination. We aimed to summarise global data on HIV and primary HCV incidence among PWID and associations with age and sex or gender. Methods: In this systematic review and meta-analysis, we updated an existing database of HIV and HCV incidence studies among PWID by searching MEDLINE, Embase, and PsycINFO, capturing studies published between Jan 1, 2000, and Dec 12, 2022, with no language or study design restrictions. We contacted authors of identified studies for unpublished or updated data. We included studies that estimated incidence by longitudinally re-testing people at risk of infection or by using assays for recent infection. We pooled incidence and relative risk (RR; young [generally defined as ≤25 years] vs older PWID; women vs men) estimates using random-effects meta-analysis and assessed risk of bias with a modified Newcastle–Ottawa scale. This study is registered with PROSPERO, CRD42020220884. Findings: Our updated search identified 9493 publications, of which 211 were eligible for full-text review. An additional 377 full-text records from our existing database and five records identified through cross-referencing were assessed. Including 28 unpublished records, 125 records met the inclusion criteria. We identified 64 estimates of HIV incidence (30 from high-income countries [HICs] and 34 from low-income or middle-income countries [LMICs]) and 66 estimates of HCV incidence (52 from HICs and 14 from LMICs). 41 (64%) of 64 HIV and 42 (64%) of 66 HCV estimates were from single cities rather than being multi-city or nationwide. Estimates were measured over 1987–2021 for HIV and 1992–2021 for HCV. Pooled HIV incidence was 1·7 per 100 person-years (95% CI 1·3–2·3; I2=98·4%) and pooled HCV incidence was 12·1 per 100 person-years (10·0–14·6; I2=97·2%). Young PWID had a greater risk of HIV (RR 1·5, 95% CI 1·2–1·8; I2=66·9%) and HCV (1·5, 1·3–1·8; I2=70·6%) acquisition than older PWID. Women had a greater risk of HIV (RR 1·4, 95% CI 1·1–1·6; I2=55·3%) and HCV (1·2, 1·1–1·3; I2=43·3%) acquisition than men. For both HIV and HCV, the median risk-of-bias score was 6 (IQR 6–7), indicating moderate risk. Interpretation: Although sparse, available HIV and HCV incidence estimates offer insights into global levels of HIV and HCV transmission among PWID. Intensified efforts are needed to keep track of the HIV and HCV epidemics among PWID and to expand access to age-appropriate and gender-appropriate prevention services that serve young PWID and women who inject drugs. Funding: Canadian Institutes of Health Research, Fonds de recherche du Québec–Santé, Canadian Network on Hepatitis C, UK National Institute for Health and Care Research, and WHO.

Original languageEnglish
Pages (from-to)533-552
Number of pages20
JournalThe Lancet Gastroenterology and Hepatology
Volume8
Issue number6
DOIs
StatePublished - Jun 2023

Bibliographical note

Publisher Copyright:
© 2023 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY 4.0 license

Funding

PV, HF, and JS acknowledge support from the US NIDA (grant numbers R01 AI147490, R01 DA033679, R01 DA037773, R21 DA046809, and R01 DA047952). PV, ZW, HF, JS, and MH are supported by the National Institute for Health and Care Research (NIHR) Health Protection Research Units in Behavioural Science and Evaluation at the University of Bristol in partnership with the UK Health Security Agency (UKHSA). MH, PV, NEP, and HF also acknowledge support from the NIHR-funded EPIToPe project. KH and KD acknowledge support from the NIDA (U01DA038886). MA acknowledges funding from the Public Health Agency of Canada and the Ministère de la santé et des services sociaux du Québec. AT acknowledges support from the Wellcome Trust. JA reports grant support through the NIH. JB holds the Canada Research Chair in Addiction Medicine and acknowledges support from the CIHR (grant numbers 175233 and 139149), FRQ-S (grant number 52905), and the NIH (R01 grant). NEP acknowledges support from Public Health Scotland. LM is supported by Australian National Health and Medical Research Council Research Fellowship GNT1154839. Acknowledgments for the members of the HIV and HCV Incidence Review Collaborative Group are provided in the appendix (p 53) .

FundersFunder number
UK Health Security Agency
NIHR-funded
Public Health Scotland
UKHSA
US NIDAR01 AI147490, R01 DA037773, R01 DA047952, R21 DA046809, R01 DA033679
National Institutes of Health (NIH)
National Institute on Drug AbuseU01DA038886
National Institute on Drug Abuse
Wellcome Trust
Public Health Agency of Canada
Ministère de la Santé et des Services sociaux
Canadian Institutes of Health Research139149, 175233
Canadian Institutes of Health Research
Fonds de Recherche du Québec-Santé52905
Fonds de Recherche du Québec-Santé
National Institute for Health and Care Research
University Hospitals Bristol NHS Foundation Trust and the University of Bristol
Australian National Health and Medical Research CouncilGNT1154839
Australian National Health and Medical Research Council
Canada Excellence Research Chairs, Government of Canada

    ASJC Scopus subject areas

    • Hepatology
    • Gastroenterology

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