Evidence map›Paper›PMID 41703097›Full record

ArticleClinical and experimental medicine2026

Subclinical cardiac dysfunction in idiopathic inflammatory myopathies: the role of global longitudinal strain.

Simone Romano, Andrea Sartorio, Chiara Dal Pont, Francesca Segatta, Marta Piazzola, Marco Vicardi, Mattia Cominacini, Federico Aldegheri, Riccardo Bixio, Ombretta Viapiana

Erratum issuedAbstract read
In one paragraph

Article in Clinical and experimental medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Simone RomanoDepartment of Internal Medicine, Section of Internal Medicine C, University of Verona, Piazzale Scuro 37134, Verona, Italy. simone.romano@univr.it.ORCID http://orcid.org/0000-0002-8623-235X
Andrea SartorioDepartment of Internal Medicine, Section of Internal Medicine C, University of Verona, Piazzale Scuro 37134, Verona, Italy.
Chiara Dal PontDepartment of Internal Medicine, Section of Internal Medicine C, University of Verona, Piazzale Scuro 37134, Verona, Italy.
Francesca SegattaDepartment of Internal Medicine, Section of Internal Medicine C, University of Verona, Piazzale Scuro 37134, Verona, Italy.
Marta PiazzolaDepartment of Internal Medicine, Section of Internal Medicine C, University of Verona, Piazzale Scuro 37134, Verona, Italy.
Marco VicardiDepartment of Internal Medicine, Section of Internal Medicine C, University of Verona, Piazzale Scuro 37134, Verona, Italy.
Mattia CominaciniDepartment of Internal Medicine, Section of Internal Medicine C, University of Verona, Piazzale Scuro 37134, Verona, Italy.
Federico AldegheriRheumatology Unit, University of Verona, Verona, Italy.
Riccardo BixioRheumatology Unit, University of Verona, Verona, Italy.
Ombretta ViapianaRheumatology Unit, University of Verona, Verona, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autoimmune diseases are characterized by systemic inflammation that can affect multiple tissues. In idiopathic inflammatory myopathies (IIM), skeletal muscle is primarily involved; however, subclinical cardiac dysfunction may also occur. While left ventricular ejection fraction (EF) is commonly used to assess cardiac function, global longitudinal strain (GLS) has proven more sensitive in detecting early myocardial impairment. This study aimed to evaluate left ventricular GLS (LV GLS) in patients with IIM and no known cardiovascular disease, assessing both the prevalence of reduced GLS values and their associations with clinical and laboratory parameters. We enrolled 37 outpatients from the Department of Internal Medicine at the University Hospital of Verona, who underwent comprehensive clinical and echocardiographic assessment. The mean GLS value observed (- 17.9% ± 2.2%) was below the normal reference range (- 18.2% to - 21.2%) defined by the echocardiographic system. When compared with 37 healthy controls, IIM patients showed significantly impaired GLS despite preserved EF in both groups (- 17.88 ± 2.23% vs. - 19.88 ± 1.72%, p < 0.001). This difference remained significant after adjusting for age and sex (β = +2.25%, p < 0.001). In linear regression models, GLS was independently associated with arthritis (β = 2.165, p = 0.007), lymphocyte count (β = 0.001, p = 0.025), CK levels (β = 0.000, p = 0.024), and age (β = 0.032, p = 0.020). Patients with arthritis showed significantly worse GLS values compared to those without arthritis, despite similar EF. In multivariate analysis, arthritis remained independently associated with impaired GLS and lower CK levels. Overall, our findings suggest that patients with IIM exhibit a global reduction in left ventricular longitudinal function, detectable by GLS, even in the absence of overt cardiac disease. This impairment appears particularly evident in patients presenting with arthritis and is independent of age-related effects. Longitudinal studies are warranted to investigate the progression of GLS alterations and their potential role in guiding therapeutic strategies.

Indexed as

Global Longitudinal StrainMyositisVentricular Dysfunction, LeftAdultAgedEchocardiographyFemaleHumansMaleMiddle AgedArthritisEchocardiographyGlobal longitudinal strainIdiopathic inflammatory myopathies

Identifiers

PMID41703097
PMCPMC12932386

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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.