Evidence map›Paper›PMID 31377134›Full record

SynthesisThe lancet. Gastroenterology & hepatology2019

Global burden of atherosclerotic cardiovascular disease in people with hepatitis C virus infection: a systematic review, meta-analysis, and modelling study.

Kuan Ken Lee, Dominik Stelzle, Rong Bing, Mohamed Anwar, Fiona Strachan, Sophia Bashir, David E Newby, Jasmit S Shah, Michael H Chung, Gerald S Bloomfield and 9 more

Open access · hybridAbstract readMeta-AnalysisSystematic Review
In one paragraph

Synthesis in The lancet. Gastroenterology & hepatology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 5 pooled it
7.9field-weighted citation impact, top 2% 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

51 citing papers in PubMed, 5 syntheses or guidelines pooled it, 104 citations in OpenAlex.

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  4. A Comprehensive Survey of the Relationship betweenArchives of Iranian medicine · 2022
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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 10 institutions in 4 countries.

Kuan Ken LeeBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
Dominik StelzleDepartment of Neurology, Center for Global Health, Technical University of Munich, Munich, Germany.
Rong BingBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
Mohamed AnwarBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
Fiona StrachanBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
Sophia BashirBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
David E NewbyBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.
Jasmit S ShahDepartment of Medicine, Aga Khan University, Nairobi, Kenya.
Michael H ChungDepartment of Medicine, Aga Khan University, Nairobi, Kenya.
Gerald S BloomfieldDepartment of Medicine, Duke Clinical Research Institute and Duke Global Health Institute, Duke University, Durham, NC, USA.
Chris T LongeneckerDivision of Cardiology, University Hospitals Harrington Heart and Vascular Institute, School of Medicine, Case Western Reserve University, Cleveland, OH, USA.
Shashwatee BagchiDivision of Infectious Diseases and Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA.
Shyamasundaran KottililDivision of Infectious Diseases and Institute of Human Virology, University of Maryland School of Medicine, Baltimore, MD, USA.
Sarah BlachCenter for Disease Analysis Foundation, Lafayette, CO, USA.
Homie RazaviCenter for Disease Analysis Foundation, Lafayette, CO, USA.
Peter R MillsDepartment of Gastroenterology, Gartnavel General Hospital, NHS Greater Glasgow and Clyde, Glasgow, UK.
Nicholas L MillsBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK; Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK.
David A McAllisterInstitute of Health and Wellbeing, University of Glasgow, Glasgow, UK.
Anoop S V ShahBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK; Usher Institute of Population Health Sciences and Informatics, University of Edinburgh, Edinburgh, UK. Electronic address: anoop.shah@ed.ac.uk.
British Heart Foundation · GBUniversity of Edinburgh · GBAga Khan University Nairobi · KECenter for Disease Analysis · USUniversity of Maryland, Baltimore · USDuke University · USNHS Greater Glasgow and Clyde · GBTechnical University of Munich · DEUniversity Hospitals of Cleveland · USUniversity of Glasgow · GB

Funding

Elucidating Hepatitis C Infection as a Risk Factor for Coronary Heart Disease in HIV-Infected PatientsK23HL133358 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI BAGCHI, SHASHWATEE · 2017 to 2021
$955k
British Heart Foundation CH/09/002/26360British Heart Foundation FS/16/14/32023British Heart Foundation FS/18/25/33454British Heart Foundation FS/19/17/34172NHLBI NIH HHS K23 HL133358Wellcome Trust 201492/Z/16/Z
6 · The paper itself

Abstract

backgroundMore than 70 million people worldwide are estimated to have hepatitis C virus (HCV) infection. Emerging evidence indicates an association between HCV and atherosclerotic cardiovascular disease. We aimed to determine the association between HCV and cardiovascular disease, and estimate the national, regional, and global burden of cardiovascular disease attributable to HCV.

methodsFor this systematic review and meta-analysis, we searched MEDLINE, Embase, Ovid Global Health, and Web of Science databases from inception to May 9, 2018, without language restrictions, for longitudinal studies that evaluated the risk ratio (RR) of cardiovascular disease in people with HCV compared with those without HCV. Two investigators independently reviewed and extracted data from published reports. The main outcome was cardiovascular disease, defined as hospital admission with, or mortality from, acute myocardial infarction or stroke. We calculated the pooled RR of cardiovascular disease associated with HCV using a random-effects model. Additionally, we calculated the population attributable fraction and disability-adjusted life-years (DALYs) from HCV-associated cardiovascular disease at the national, regional, and global level. We also used age-stratified and sex-stratified HCV prevalence estimates and cardiovascular DALYs for 100 countries to estimate country-level burden associated with HCV. This study is registered with PROSPERO, number CRD42018091857.

findingsOur search identified 16 639 records, of which 36 studies were included for analysis, including 341 739 people with HCV. The pooled RR for cardiovascular disease was 1·28 (95% CI 1·18-1·39). Globally, 1·5 million (95% CI 0·9-2·1) DALYs per year were lost due to HCV-associated cardiovascular disease. Low-income and middle-income countries had the highest disease burden with south Asian, eastern European, north African, and Middle Eastern regions accounting for two-thirds of all HCV-associated cardiovascular DALYs.

interpretationHCV infection is associated with an increased risk of cardiovascular disease. The global burden of cardiovascular disease associated with HCV infection was responsible for 1·5 million DALYs, with the highest burden in low-income and middle-income countries.

fundingBritish Heart Foundation and Wellcome Trust.

Indexed as

AtherosclerosisGlobal Burden of DiseaseHepatitis C, ChronicHumansPrevalenceQuality-Adjusted Life YearsRisk Assessment

Identifiers

PMID31377134
PMCPMC6734111
OpenAlexW2965243229

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.