Coronary plaque in people with HIV vs non-HIV asymptomatic community and symptomatic higher-risk populationsCardiovascular Imaging Research Center, Massachusetts General Hospital & Harvard Medical School, MA, Boston, United States; Faculty of Medicine, Department of Radiology, Medical Center-University of Freiburg, University of Freiburg, Freiburg im Breisgau, Germany.
Cardiovascular Imaging Research Center, Massachusetts General Hospital & Harvard Medical School, MA, Boston, United States.
Cardiovascular Imaging Research Center, Massachusetts General Hospital & Harvard Medical School, MA, Boston, United States.
Metabolism Unit, Massachusetts General Hospital & Harvard Medical School, MA, Boston, United States.
Department of Medicine, Icahn School of Medicine at Mount Sinai, NY, New York, United States.
Department of Medicine, University of California at Los Angeles, CA, Los Angeles, United States.
Metabolism Unit, Massachusetts General Hospital & Harvard Medical School, MA, Boston, United States.
Metabolism Unit, Massachusetts General Hospital & Harvard Medical School, MA, Boston, United States.
Duke Clinical Research Institute, Duke University School of Medicine, NC, Durham, United States.
Division of Infectious Diseases, University of Alabama at Birmingham, AL, Birmingham, United States.
Division of Clinical Epidemiology, Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
Faculty of Medicine and Health Sciences, Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden; Center of Medical Image Science and Visualization, Linköping University, Linköping, Sweden.
Department of Translational Medicine, Lund University, Malmö, Sweden; Department of Infectious Diseases, Växjö Central Hospital, Växjö, Sweden.
Division of Cardiovascular Medicine, Department of Clinical Sciences, Danderyd Hospital, Karolinska Institute, Stockholm, Sweden.
Cooper University Hospital, NJ, Camden, United States.
Division of Infectious Diseases, University of Southern California Keck School of Medicine, CA, Los Angeles, United States.
Section of Infectious Disease, Tulane School of Medicine, LA, New Orleans, United States.
Division of Infectious Diseases, University of Cincinnati, OH, Cincinnati, United States.
Division of Infectious Diseases, The Ohio State University Wexner Medical Center, OH, Columbus, United States.
Metabolism Unit, Massachusetts General Hospital & Harvard Medical School, MA, Boston, United States.
Cardiovascular Imaging Research Center, Massachusetts General Hospital & Harvard Medical School, MA, Boston, United States; Innovative Imaging Consulting LLC, MA, Boston, United States.
Center for Biostatistics in AIDS Research, Harvard T.H. Chan School of Public Health, MA, Boston, United States.
Metabolism Unit, Massachusetts General Hospital & Harvard Medical School, MA, Boston, United States.
Duke Clinical Research Institute, Duke University School of Medicine, NC, Durham, United States.
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2024 (English)In: JACC: Advances, E-ISSN 2772-963X, Vol. 3, no 6, article id 100968Article in journal (Refereed) Published
Abstract [en]
Background: People with HIV (PWH) have a high burden of coronary plaques; however, the comparison to people without known HIV (PwoH) needs clarification.
Objectives: The purpose of this study was to determine coronary plaque burden/phenotype in PWH vs PwoH.
Methods: Nonstatin using participants from 3 contemporary populations without known coronary plaques with coronary CT were compared: the REPRIEVE (Randomized Trial to Prevent Vascular Events in HIV) studying PWH without cardiovascular symptoms at low-to-moderate risk (n = 755); the SCAPIS (Swedish Cardiopulmonary Bioimage Study) of asymptomatic community PwoH at low-to-intermediate cardiovascular risk (n = 23,558); and the PROMISE (Prospective Multicenter Imaging Study for Evaluation of Chest Pain) of stable chest pain PwoH (n = 2,291). The coronary plaque prevalence on coronary CT was compared, and comparisons were stratified by 10-year atherosclerotic cardiovascular disease (ASCVD) risk, age, and coronary artery calcium (CAC) presence.
Results: Compared to SCAPIS and PROMISE PwoH, REPRIEVE PWH were younger (50.8 ± 5.8 vs 57.3 ± 4.3 and 60.0 ± 8.0 years; P < 0.001) and had lower ASCVD risk (5.0% ± 3.2% vs 6.0% ± 5.3% and 13.5% ± 11.0%; P < 0.001). More PWH had plaque compared to the asymptomatic cohort (48.5% vs 40.3%; P < 0.001). When stratified by ASCVD risk, PWH had more plaque compared to SCAPIS and a similar prevalence of plaque compared to PROMISE. CAC = 0 was more prevalent in PWH (REPRIEVE 65.2%; SCAPIS 61.6%; PROMISE 49.6%); among CAC = 0, plaque was more prevalent in PWH compared to the PwoH cohorts (REPRIEVE 20.8%; SCAPIS 5.4%; PROMISE 12.3%, P < 0.001).
Conclusions: Asymptomatic PWH in REPRIEVE had more plaque than asymptomatic PwoH in SCAPIS but had similar prevalence to a higher-risk stable chest pain cohort in PROMISE. In PWH, CAC = 0 does not reliably exclude plaque.
Place, publisher, year, edition, pages
Elsevier, 2024. Vol. 3, no 6, article id 100968
Keywords [en]
asymptomatic community cohort, cardiovascular disease, coronary CT angiography, coronary plaque, people with HIV, stable chest pain
National Category
Cardiology and Cardiovascular Disease General Practice
Identifiers
URN: urn:nbn:se:umu:diva-228064DOI: 10.1016/j.jacadv.2024.100968Scopus ID: 2-s2.0-85191779675OAI: oai:DiVA.org:umu-228064DiVA, id: diva2:1887006
Projects
SCAPIS
Funder
NIH (National Institutes of Health), U01HL123336NIH (National Institutes of Health), U01HL123339Swedish Heart Lung FoundationKnut and Alice Wallenberg FoundationVinnova2024-08-062024-08-062025-02-10Bibliographically approved