Evidence map›Paper›PMID 27105648›Full record

ArticleHeart (British Cardiac Society)2016

Short-term and long-term cardiovascular risk, metabolic syndrome and HIV in Tanzania.

Justin R Kingery, Yona Alfred, Luke R Smart, Emily Nash, Jim Todd, Mostafa R Naguib, Jennifer A Downs, Samuel Kalluvya, Johannes B Kataraihya, Robert N Peck

Abstract readComparative Study
In one paragraph

Article in Heart (British Cardiac Society), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 4 pooled it
–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

28 citing papers in PubMed, 4 syntheses or guidelines pooled it.

  1. Pooled it
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  8. Observational
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  15. Circulating Hydrogen Sulfide (HJournal of clinical medicine · 2021
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Justin R KingeryDepartment of Internal Medicine, Catholic University of Health and Allied Sciences, Mwanza, Tanzania Department of Internal Medicine, Bugando Medical Centre, Mwanza, Tanzania Division of Hospital Medicine, Department of Internal Medicine, Weill Cornell Medical College, New York City, New York, USA Department of Internal Medicine, Center for Global Health, Weill Cornell Medical College, New York City, New York, USA.
Yona AlfredDepartment of Internal Medicine, Catholic University of Health and Allied Sciences, Mwanza, Tanzania Department of Internal Medicine, Bugando Medical Centre, Mwanza, Tanzania.
Luke R SmartDepartment of Internal Medicine, Catholic University of Health and Allied Sciences, Mwanza, Tanzania Department of Internal Medicine, Bugando Medical Centre, Mwanza, Tanzania Department of Internal Medicine, Center for Global Health, Weill Cornell Medical College, New York City, New York, USA.
Emily NashDepartment of Internal Medicine, Center for Global Health, Weill Cornell Medical College, New York City, New York, USA.
Jim ToddPopulation Health Department, London School of Hygiene & Tropical Medicine, London, UK.
Mostafa R NaguibDepartment of Medicine, Weill Cornell Medical College-Qatar, Doha, Qatar.
Jennifer A DownsDepartment of Internal Medicine, Catholic University of Health and Allied Sciences, Mwanza, Tanzania Department of Internal Medicine, Bugando Medical Centre, Mwanza, Tanzania Department of Internal Medicine, Center for Global Health, Weill Cornell Medical College, New York City, New York, USA.
Samuel KalluvyaDepartment of Internal Medicine, Catholic University of Health and Allied Sciences, Mwanza, Tanzania Department of Internal Medicine, Bugando Medical Centre, Mwanza, Tanzania.
Johannes B KataraihyaDepartment of Internal Medicine, Catholic University of Health and Allied Sciences, Mwanza, Tanzania Department of Internal Medicine, Bugando Medical Centre, Mwanza, Tanzania.
Robert N PeckDepartment of Internal Medicine, Catholic University of Health and Allied Sciences, Mwanza, Tanzania Department of Internal Medicine, Bugando Medical Centre, Mwanza, Tanzania Division of Hospital Medicine, Department of Internal Medicine, Weill Cornell Medical College, New York City, New York, USA Department of Internal Medicine, Center for Global Health, Weill Cornell Medical College, New York City, New York, USA.

Funding

TUBERCULOSIS INTERNATIONAL TRAINING AND RESEARCH PROGRAMD43TW000018 · FIC · WEILL MEDICAL COLL OF CORNELL UNIV · PI JOHNSON, WARREN DOUGLAS · 1988 to 2012
$16.1M
Vanderbilt-Emory-Cornell-Duke Consortium for Global Health Fellows (VECDor)R25TW009337 · FIC · VANDERBILT UNIVERSITY MEDICAL CENTER · PI HEIMBURGER, DOUGLAS CORBETT, VERMUND, STEN H. · 2012 to 2016
$6.3M
Global Health Research Training in HIV and TuberculosisK24AI098627 · NIAID · WEILL MEDICAL COLL OF CORNELL UNIV · PI FITZGERALD, DANIEL W · 2012 to 2022
$1.8M
Hypertension in HIV-Infected Tanzanians: Time Course and PathogenesisK01TW010281 · FIC · WEILL MEDICAL COLL OF CORNELL UNIV · PI PECK, ROBERT N · 2015 to 2019
$689k
FIC NIH HHS D43 TW000018FIC NIH HHS K01 TW010281FIC NIH HHS R25 TW009337NIAID NIH HHS K24 AI098627
6 · The paper itself

Abstract

objectiveTo compare short-term and long-term cardiovascular disease (CVD) risk scores and prevalence of metabolic syndrome in HIV-infected adults receiving and not receiving antiretroviral therapy (ART) to HIV-negative controls.

methodsA cross-sectional study including 151 HIV-infected, ART-naive, 150 HIV-infected on ART and 153 HIV-negative adults. Traditional cardiovascular risk factors were determined by standard investigations. The primary outcome was American College of Cardiology/American Heart Association Atherosclerotic CVD (ASCVD) Risk Estimator lifetime CVD risk score. Secondary outcomes were ASCVD 10-year risk, Framingham risk scores, statin indication and metabolic syndrome.

resultsCompared with HIV-negative controls, more HIV-infected adults on ART were classified as high lifetime CVD risk (34.7% vs 17.0%, p<0.001) although 10-year risk scores were similar, a trend which was similar across multiple CVD risk models. In addition, HIV-infected adults on ART had a higher prevalence of metabolic syndrome versus HIV-negative controls (21.3% vs 7.8%, p=0.008), with two common clusters of risk factors. More than one-quarter (28.7%) of HIV-infected Tanzanian adults on ART meet criteria for statin initiation.

conclusionsHIV-infected ART-treated individuals have high lifetime cardiovascular risk, and this risk seems to develop rapidly in the first 3-4 years of ART as does the development of clusters of metabolic syndrome criteria. These data identify a new subgroup of low short-term/high-lifetime risk HIV-infected individuals on ART who do not currently meet criteria for CVD risk factor modification but require further study.

Indexed as

AdultCardiovascular DiseasesCase-Control StudiesCross-Sectional StudiesFemaleHIV InfectionsHumansHydroxymethylglutaryl-CoA Reductase InhibitorsMaleMetabolic SyndromeMiddle AgedPrevalencePrognosisRisk AssessmentRisk FactorsTanzaniaHydroxymethylglutaryl-CoA Reductase Inhibitors

Identifiers

PMID27105648
PMCPMC4945369

What OpenQuestion holds

Texttitle and abstract
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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.