Evidence map›Paper›PMID 34372666›Full record

ArticleCirculation. Heart failure2021

Long-Term Trajectories of Left Ventricular Ejection Fraction in Patients With Chronic Inflammatory Diseases and Heart Failure: An Analysis of Electronic Health Records.

Adovich S Rivera, Arjun Sinha, Faraz S Ahmad, Edward Thorp, Jane E Wilcox, Donald M Lloyd-Jones, Matthew J Feinstein

Open access · bronzeAbstract read
In one paragraph

Article in Circulation. Heart failure, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.3field-weighted citation impact, top 19% 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

11 citing papers in PubMed, 12 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

7 authors at 1 institution in 1 country.

Adovich S RiveraInstitute for Public Health and Medicine (A.S.R.), Northwestern University Feinberg School of Medicine, Chicago, IL.
Arjun SinhaDivision of Cardiology, Department of Medicine (A.S., F.S.A., J.E.W., D.M.L.-J., M.J.F.), Northwestern University Feinberg School of Medicine, Chicago, IL.
Faraz S AhmadDivision of Cardiology, Department of Medicine (A.S., F.S.A., J.E.W., D.M.L.-J., M.J.F.), Northwestern University Feinberg School of Medicine, Chicago, IL.
Edward ThorpDepartment of Pathology (E.T.), Northwestern University Feinberg School of Medicine, Chicago, IL.
Jane E WilcoxDivision of Cardiology, Department of Medicine (A.S., F.S.A., J.E.W., D.M.L.-J., M.J.F.), Northwestern University Feinberg School of Medicine, Chicago, IL.
Donald M Lloyd-JonesDivision of Cardiology, Department of Medicine (A.S., F.S.A., J.E.W., D.M.L.-J., M.J.F.), Northwestern University Feinberg School of Medicine, Chicago, IL.
Matthew J FeinsteinDivision of Cardiology, Department of Medicine (A.S., F.S.A., J.E.W., D.M.L.-J., M.J.F.), Northwestern University Feinberg School of Medicine, Chicago, IL.
Northwestern University · US

Funding

Northwestern University Clinical and Translational Science Institute (NUCATS)UL1TR001422 · NCATS · NORTHWESTERN UNIVERSITY AT CHICAGO · PI D'AQUILA, RICHARD · 2015 to 2023
$56.8M
Virology and Immunology Technology CoreP30AI117943 · NIAID · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Michael E Newcomb · 2015 to 2026
$38.4M
Efferocytosis-Directed Inflammation Resolution and Repair in the Hypoxic HeartR01HL122309 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI THORP, EDWARD BENJAMIN · 2014 to 2024
$5.0M
Myocardial Vulnerability to Ischemia-Induced Dysfunction and Heart Failure: The Impact of HIV/SIV, ART, and Targeted ImmunotherapyR01HL154862 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI FEINSTEIN, MATTHEW JOEL, VASILE PANDREA, IVONA · 2020 to 2023
$3.1M
Immunologic, Inflammatory, and Clinical contributors to HIV-Related Heart Failure with Preserved Ejection Fraction (HFpEF)R01HL156792 · NHLBI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI FEINSTEIN, MATTHEW JOEL · 2021 to 2024
$2.9M
AHRQ HHS K12 HS026385NCATS NIH HHS UL1 TR001422NHLBI NIH HHS R01 HL122309NHLBI NIH HHS R01 HL154862NHLBI NIH HHS R01 HL156792NIAID NIH HHS P30 AI117943
6 · The paper itself

Abstract

backgroundImmune regulation and inflammation play a role in the pathogenesis and progression of acute and chronic heart failure (HF). Although the clinical course of acute, severe inflammatory cardiomyopathy is well described, the effects of chronic systemic inflammation on cardiovascular function over time are less clear. To investigate this question, we compared trajectories over time in left ventricular ejection fraction for patients with HF with different chronic inflammatory diseases (CIDs): HIV, systemic lupus erythematosus, systemic sclerosis, rheumatoid arthritis, inflammatory bowel disease, and/or psoriasis.

methodsUsing a database of patients receiving care in a large metropolitan health care system since January 1, 2000, we analyzed serial, clinically indicated echocardiograms from patients with HF with CIDs and frequency-matched patients with HF without CIDs. We included patients with ≥3 serial echocardiograms (N=974; median 6.1 years between first and most recent echo). We assessed left ventricular ejection fraction trajectories over time using latent trajectory models, then investigated differences in left ventricular ejection fraction trajectories for specific CID subtypes compared with controls.

resultsOverall, the majority of patients studied (N=687; 70.5%) had left ventricular ejection fraction trajectories consistent with HF with preserved or midrange EF, whereas 255 (26.2%) had HF with reduced EF and 32 (3.3%) had HF with recovered EF. Compared with non-CID controls with HF, patients with rheumatoid arthritis, inflammatory bowel disease, and systemic lupus erythematosus were significantly more likely than controls to have HF with preserved or midrange EF whereas patients with HIV were significantly more likely to have HF with reduced EF.

conclusionsAmong patients with HF with CIDs, distinct left ventricular ejection fraction trajectory patterns associate with different specific individual CIDs. This highlights the heterogeneity of HF subtypes and changes over time across different CIDs.

Indexed as

Electronic Health RecordsAdultAgedChronic DiseaseEchocardiographyFemaleHeart FailureHumansMaleMiddle AgedRisk FactorsStroke VolumeVentricular Function, Leftautoimmune diseasescardiomyopathyheart failureinflammationpsoriasis

Identifiers

PMID34372666
PMCPMC8373674
OpenAlexW3192557299

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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.