Evidence map›Paper›PMID 40064403›Full record

ArticleJournal of the American Society of Echocardiography : official publication of the American Society of Echocardiography2025

Clinical Risk Predictors for Abnormal Left Ventricular and Atrial Function in Lupus Erythematosus.

Matteo Morello, Bethany Gholson, Weiting Huang, William Lain, Maxwell Malter, Antonio Abbate, Brittany N Weber, Jonathan R Lindner

Abstract read
In one paragraph

Article in Journal of the American Society of Echocardiography : official publication of the American Society of Echocardiography, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

8 authors.

Matteo MorelloCardiovascular Division and Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, Virginia.
Bethany GholsonCardiovascular Division and Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, Virginia.
Weiting HuangCardiovascular Division and Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, Virginia.
William LainCardiovascular Division and Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, Virginia.
Maxwell MalterCardiovascular Division and Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, Virginia.
Antonio AbbateCardiovascular Division and Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, Virginia.
Brittany N WeberHeart and Vascular Center and Division of Preventive Cardiology, Brigham and Women's Hospital, Boston, Massachusetts.
Jonathan R LindnerCardiovascular Division and Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, Virginia. Electronic address: jlindner@virginia.edu.

Funding

Augmentation of Tissue Perfusion with Ultrasound-mediated CavitationR01HL130046 · NHLBI · UNIVERSITY OF VIRGINIA · PI LINDNER, JONATHAN R · 2016 to 2023
$5.5M
Advanced Non-invasive Imaging in the Investigation of Aortic Stenosis PathobiologyR01HL165422 · NHLBI · UNIVERSITY OF VIRGINIA · PI Jonathan R Lindner · 2022 to 2026
$3.5M
Ultrasound Cavitation for Facilitated Cardiac Transduction of AAVR01HL171377 · NHLBI · UNIVERSITY OF VIRGINIA · PI Brent A French, Jonathan R Lindner · 2024 to 2026
$2.1M
Biodefense Short-Term Training for Minority StudentT35AI060528 · NIAID · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI HALME, ADRIAN J, PETRI, WILLIAM A · 2004 to 2024
$1.3M
Advanced CV imaging and immunophenotyping to study coronary vascular health in psoriasisK23HL159276 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI WEBER, BRITTANY NICOLE · 2021 to 2025
$962k
NHLBI NIH HHS K23 HL159276NHLBI NIH HHS R01 HL130046NHLBI NIH HHS R01 HL165422NHLBI NIH HHS R01 HL171377NIAID NIH HHS T35 AI060528
6 · The paper itself

Abstract

backgroundIn systemic lupus erythematosus (SLE), ventricular dysfunction can occur from primary immune injury or secondarily from SLE-related comorbidities. The aim of this study was to determine clinical predictors of reduced left ventricular (LV) systolic and diastolic function in an effort to understand potentially mitigating strategies.

methodsThe authors retrospectively studied 76 patients with SLE who underwent comprehensive transthoracic echocardiography within 3 months of an appointment with a rheumatologist to correlate clinical, laboratory, and echocardiographic features. All key echocardiographic measurements were reviewed and remeasured, when appropriate, by an expert blinded to other study data. Abnormal LV systolic function was defined as a global longitudinal strain threshold of -18.0%. Hierarchical cluster analysis was used to define feature interaction.

resultsThe mean age of the population was 49 ± 15 years, and 83% were women. Reduced GLS was found in 24% of the population, of whom 44% had LV ejection fractions <50%. Previously documented heart failure symptoms were more prevalent in the reduced GLS cohort (50% vs 12%, P = .002). Those with reduced GLS had clinical features indicating greater SLE severity over time, including reduced renal function and prior pericardial involvement. GLS was strongly associated with right ventricular free wall strain (r = 0.67, P < .01) and degree of LV diastolic dysfunction. Worsening grades of diastolic dysfunction, like GLS, were associated with renal disease and pericardial involvement. Patients with SLE with reduced GLS and diastolic function also had abnormal left atrial reservoir strain (LASr). Hierarchical cluster analysis segregated populations with reduced GLS, reduced LASr, pericardial and renal involvement, and an additional feature of C-reactive protein known to be associated with chronic disease activity.

conclusionsReduced GLS is common in patients with SLE and is associated with heart failure symptoms and markers of increased disease activity over time, particularly pericardial involvement, suggesting common immune mechanisms. The associations of GLS with right ventricular function, diastolic dysfunction, and impairment in LASr suggests a common mechanistic basis involving immune injury.

Indexed as

EchocardiographyLupus Erythematosus, SystemicVentricular Dysfunction, LeftAdultFemaleHumansMaleMiddle AgedReproducibility of ResultsRetrospective StudiesRisk AssessmentRisk FactorsStroke VolumeEchocardiographyLeft atrial strainLeft ventricular strainSystemic lupus erythematosus

Identifiers

PMID40064403
PMCPMC12208098

What Socratic holds

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LicenceTDM
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 Socratic graph.