Evidence mapPaperPMID 41378479Full record

Observational studyJournal of the American Heart Association2025

Baseline ECG and Cardiovascular Outcomes in People With HIV: Insights From REPRIEVE.

Aya Awwad, Christopher de Filippi, Heather Ribaudo, Markella V Zanni, Carl J Fichtenbaum, Carlos D Malvestutto, Judith A Aberg, Marissa R Diggs, Sarah M Chu, Alex B Lu and 11 more

Abstract readObservational Study
In one paragraph

Observational study in Journal of the American Heart Association, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

21 authors.

Aya AwwadMetabolism Unit Massachusetts General Hospital and Harvard Medical School Boston MA USA.ORCID 0000-0003-4452-3498
Christopher de FilippiInova Schar Heart and Vascular Falls Church VA USA.ORCID 0000-0002-0660-4943
Heather RibaudoCenter for Biostatistics in AIDS Research, Harvard T.H. Chan School of Public Health Boston MA USA.ORCID 0000-0002-0394-3990
Markella V ZanniMetabolism Unit Massachusetts General Hospital and Harvard Medical School Boston MA USA.ORCID 0000-0002-4711-3956
Carl J FichtenbaumDivision of Infectious Diseases University of Cincinnati College of Medicine Cincinnati OH USA.ORCID 0000-0002-6778-7253
Carlos D MalvestuttoDivision of Infectious Diseases Ohio State University Medical Center Columbus OH USA.ORCID 0000-0003-3156-2965
Judith A AbergDivision of Infectious Diseases Icahn School of Medicine at Mount Sinai New York NY USA.ORCID 0000-0001-8162-0284
Marissa R DiggsMetabolism Unit Massachusetts General Hospital and Harvard Medical School Boston MA USA.
Sarah M ChuMetabolism Unit Massachusetts General Hospital and Harvard Medical School Boston MA USA.
Alex B LuMetabolism Unit Massachusetts General Hospital and Harvard Medical School Boston MA USA.
Craig A SponsellerKowa Pharmaceuticals America, Inc. Montgomery AL USA.
Shashwatee BagchiDivision of Infectious Diseases Washington University School of Medicine St. Louis MO USA.ORCID 0000-0002-8043-8605
Celestine WanjallaDivision of Infectious Diseases Vanderbilt University Medical Center Nashville TN USA.ORCID 0000-0001-9159-5414
Graham SmithMaple Leaf Medical Clinic Toronto ON Canada.
Kara W ChewDivision of Infectious Diseases, Department of Medicine David Geffen School of Medicine at University of California, Los Angeles Los Angeles CA USA.ORCID 0000-0003-4865-4348
Judith S CurrierDivision of Infectious Diseases, Department of Medicine David Geffen School of Medicine at University of California, Los Angeles Los Angeles CA USA.ORCID 0000-0003-4279-4737
Sophia ZhaoMetabolism Unit Massachusetts General Hospital and Harvard Medical School Boston MA USA.ORCID 0009-0002-5828-0706
Michael T LuCardiovascular Imaging Research Center Massachusetts General Hospital and Harvard Medical School Boston MA USA.ORCID 0000-0003-4696-9610
Pamela S DouglasDepartment of Medicine and Duke Clinical Research Institute Duke University Durham NC USA.ORCID 0000-0001-9876-4049
Steven K GrinspoonMetabolism Unit Massachusetts General Hospital and Harvard Medical School Boston MA USA.
Gerald S BloomfieldDepartment of Medicine and Duke Clinical Research Institute Duke University Durham NC USA.ORCID 0000-0002-7176-1611

Funding

Statistical and Data Management Center (SDMC), AIDS Clinical Trials Group (ACTG)UM1AI068634 · NIAID · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · 2021 to 2025
$81.6M
UCLA AIDS Prevention and Treatment Clinical Trials UnitUM1AI069424 · NIAID · UNIVERSITY OF CALIFORNIA LOS ANGELES · 2021 to 2025
$22.2M
ROLE OF DIETARY CONSTITUENTS ON GENE EXPRESSION IN INTESTINAL EPITHELIUMP30DK040561 · MASSACHUSETTS GENERAL HOSPITAL · 1994 to 2025
$6.0M
NIAID NIH HHS UM1 AI068634NIAID NIH HHS UM1 AI069424NIDDK NIH HHS P30 DK040561
6 · The paper itself

Abstract

backgroundWith antiretroviral therapy, people with HIV (PWH) have an increased burden of cardiovascular disease. The REPRIEVE (Randomized Trial to Prevent Vascular Events in HIV) trial demonstrated that pitavastatin reduces major adverse cardiovascular events (MACEs) among PWH at low to moderate traditional atherosclerotic risk. Electrocardiographic abnormalities are common in PWH, but little is known about their association with MACEs. We sought to examine whether baseline electrocardiographic abnormalities are associated with increased MACE risk among a global primary cardiovascular disease prevention cohort of PWH in REPRIEVE.

methodsIn this observational analysis, entry electrocardiographic abnormalities were adjudicated and classified as major or minor abnormalities. Multivariable cause-specific Cox proportional hazards models assessed the association of electrocardiographic abnormalities with MACEs while stratifying for treatment effect. The model improvement with the addition of the ECG to a model with the pooled cohort equations risk score was examined.

resultsAmong 7719 participants (median age, 50 years; 69% men), 49% had ≥1 electrocardiographic abnormality, with 3% classified as major. Over a median of 5.6 years, a major electrocardiographic abnormality was associated with a 2.42-fold (95% CI, 1.49-3.91) higher hazard of incident MACEs, whereas minor abnormalities were not. Specific abnormalities associated with MACEs were chamber enlargement and infarct/ischemia pattern. No significant subgroup- or treatment-related interaction was observed. Adding electrocardiographic findings to traditional risk factors increased the C-statistic modestly (+0.01).

conclusionsAmong PWH in REPRIEVE, electrocardiographic abnormalities were common, but major electrocardiographic abnormalities were rare. Though major abnormalities were associated with increased hazard of MACEs, routine electrocardiographic screening is unlikely to improve the prediction of future cardiovascular events in this primary prevention population with low to moderate cardiovascular risk.

Indexed as

Cardiovascular DiseasesElectrocardiographyHIV InfectionsAdultAnti-HIV AgentsFemaleHeart Disease Risk FactorsHumansMaleMiddle AgedMulticenter Studies as TopicRandomized Controlled Trials as TopicRisk AssessmentRisk FactorsAnti-HIV AgentsECGHIVrisk stratificationscreening

Identifiers

PMID41378479
PMCPMC12826942

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.