Evidence map›Paper›PMID 36688465›Full record

ArticleClinical infectious diseases : an official publication of the Infectious Diseases Society of America2023

Leukocyte Count and Coronary Artery Disease Events in People With Human Immunodeficiency Virus: A Longitudinal Study.

Emma F Avery, Julia N Kleynhans, Bruno Ledergerber, Isabella C Schoepf, Christian W Thorball, Neeltje A Kootstra, Peter Reiss, Lene Ryom, Dominique L Braun, Maria C Thurnheer and 10 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical infectious diseases : an official publication of the Infectious Diseases Society of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

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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

20 authors at 12 institutions in 3 countries.

Emma F AveryUniversity Department of Medicine and Infectious Diseases Service, Kantonsspital Baselland, University of Basel, Bruderholz, Switzerland.
Julia N KleynhansUniversity Department of Medicine and Infectious Diseases Service, Kantonsspital Baselland, University of Basel, Bruderholz, Switzerland.
Bruno LedergerberDivision of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Isabella C SchoepfUniversity Department of Medicine and Infectious Diseases Service, Kantonsspital Baselland, University of Basel, Bruderholz, Switzerland.
Christian W ThorballPrecision Medicine Unit, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Neeltje A KootstraDepartment of Experimental Immunology, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
Peter ReissDepartment of Global Health and Division of Infectious Disease, Amsterdam University Medical Centers, University of Amsterdam, and Amsterdam Institute for Global Health and Development, Amsterdam, The Netherlands.
Lene RyomCentre of Excellence for Health, Immunity, and Infections, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark.
Dominique L BraunDivision of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Maria C ThurnheerDepartment of Infectious Diseases, Bern University Hospital, University of Bern, Bern, Switzerland.
Catia MarzoliniDivision of Infectious Diseases and Hospital Epidemiology, University Hospital Basel, Basel, Switzerland.
Marco SeneghiniDivision of Infectious Diseases, Kantonsspital St Gallen, St. Gallen, Switzerland.
Enos BernasconiDivision of Infectious Diseases, Ospedale Regionale Lugano, University of Geneva and Università della Svizzera italiana, Lugano, Switzerland.
Matthias CavassiniInfectious Diseases Service, Lausanne University Hospital, University of Lausanne, Lausanne, Switzerland.
Hélène BuvelotDivision of Infectious Disease, Geneva University Hospital, Geneva, Switzerland.
Roger D KouyosDivision of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Jacques FellayPrecision Medicine Unit, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Huldrych F GünthardDivision of Infectious Diseases and Hospital Epidemiology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
Philip E TarrUniversity Department of Medicine and Infectious Diseases Service, Kantonsspital Baselland, University of Basel, Bruderholz, Switzerland.ORCID 0000-0002-1488-5407
Swiss HIV Cohort Study
University of Basel · CHUniversity of Zurich · CHUniversity of Lausanne · CHÉcole Polytechnique Fédérale de Lausanne · CHOspedale regionale di Lugano · CHUniversity Hospital of Basel · CHUniversity Hospital of Geneva · CHUniversity of Bern · CHAmsterdam Institute for Global Health and Development · NLAmsterdam University Medical Centers · NLKantonsspital St. Gallen · CHUniversity of Copenhagen · DK

Funding

Swiss National Science Foundation 201369
6 · The paper itself

Abstract

backgroundPeople with human immunodeficiency virus (HIV; PWH) have increased cardiovascular risk. Higher leukocyte count has been associated with coronary artery disease (CAD) events in the general population. It is unknown whether the leukocyte-CAD association also applies to PWH.

methodsIn a case-control study nested within the Swiss HIV Cohort Study, we obtained uni- and multivariable odds ratios (OR) for CAD events, based on traditional and HIV-related CAD risk factors, leukocyte count, and confounders previously associated with leukocyte count.

resultsWe included 536 cases with a first CAD event (2000-2021; median age, 56 years; 87% male; 84% with suppressed HIV RNA) and 1464 event-free controls. Cases had higher latest leukocyte count before CAD event than controls (median [interquartile range], 6495 [5300-7995] vs 5900 [4910-7200]; P < .01), but leukocytosis (>11 000/µL) was uncommon (4.3% vs 2.1%; P = .01). In the highest versus lowest leukocyte quintile at latest time point before CAD event, participants had univariable CAD-OR = 2.27 (95% confidence interval, 1.63-3.15) and multivariable adjusted CAD-OR = 1.59 (1.09-2.30). For comparison, univariable CAD-OR for dyslipidemia, diabetes, and recent abacavir exposure were 1.58 (1.29-1.93), 2.19 (1.59-3.03), and 1.73 (1.37-2.17), respectively. Smoking and, to a lesser degree, alcohol and ethnicity attenuated the leukocyte-CAD association. Leukocytes measured up to 8 years before the event were significantly associated with CAD events.

conclusionsPWH in Switzerland with higher leukocyte counts have an independently increased risk of CAD events, to a degree similar to traditional and HIV-related risk factors.

Indexed as

Coronary Artery DiseaseHIV InfectionsCase-Control StudiesCohort StudiesFemaleHIVHumansLeukocyte CountLongitudinal StudiesMaleMiddle AgedRisk Factorscoronary artery diseaseHIV infectionleukocytesmultivariable analysiswhite blood cells

Identifiers

PMID36688465
PMCPMC10249993
OpenAlexW4317776833

What OpenQuestion holds

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LicenceCC BY
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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.