Key result
Rheumatoid arthritis with normal LVEF is linked to diminished GLS indicating subclinical myocardial dysfunction.
Why the study?
Traditional echocardiography often overlooks early myocardial failure in rheumatoid arthritis, prompting investigation into whether speckle tracking echocardiography can identify subclinical left ventricular systolic dysfunction in patients with normal left ventricular function.
Does speckle tracking echocardiography identify subclinical myocardial dysfunction in rheumatoid arthritis patients with normal left ventricular function compared to healthy controls?
Cross-Sectional (n=72)
Single-blind
No
Does speckle tracking echocardiography identify subclinical myocardial dysfunction in rheumatoid arthritis patients with normal left ventricular function compared to healthy controls?
Absolute Event Rate: -18.99% vs -20.42%
p-value: p=0.015
Speckle tracking echocardiography can detect subclinical left ventricular systolic dysfunction in a significant proportion of rheumatoid arthritis patients with normal ejection fractions, with anemia serving as a strong independent predictor.
Speckle tracking may identify subclinical LV dysfunction in RA with preserved EF; hypothesis-generating and should not yet change practice.
Background: Rheumatoid arthritis (RA) is a chronic inflammatory condition recognized for elevating cardiovascular morbidity and mortality, even in the absence of overt cardiovascular symptoms. Traditional echocardiogram frequently overlooks early myocardial failure, necessitating more sensitive imaging modalities, such as speckle tracking echocardiography (STE), to effectively diagnose subclinical left ventricular systolic dysfunction (LVSD). Timely identification of cardiac involvement is essential for reducing long-term cardiovascular risks in people with rheumatoid arthritis. Objectives: This study sought to (i) determine if STE can identify subclinical myocardial dysfunction in RA Patients with normal left ventricular function as assessed by transthoracic echocardiography and (ii) identify clinical and biological factors linked to this extra-articular manifestation. Methods: A total of 36 RA patients and 36 matching healthy controls were included. All subjects underwent standard transthoracic echocardiogram and speckle tracking STE to evaluate left ventricular function. Global longitudinal strain (GLS) was employed to identify subclinical left ventricular systolic dysfunction, with a GLS threshold of ≤ - 18% signifying LVSD. Clinical and biochemical variables, such as hemoglobin concentrations, diabetes mellitus, and disease activity (DAS28-CRP), were evaluated to determine their correlation with compromised myocardial strain. Results: = 0.016), although diabetes mellitus and age exhibited associations with myocardial strain in univariate analysis. No substantial correlations were identified between GLS and disease activity (DAS28-CRP) or immunological markers (RF, anti-CCP). Conclusion: STE identified subclinical LVSD in a significant number of RA patients with normal LVEF, emphasizing its effectiveness in early cardiovascular risk assessment. Hemoglobin levels were a crucial predictor of subclinical LVSD, highlighting the necessity of thorough cardiovascular risk evaluations in RA, especially for individuals with anemia or other concomitant conditions. Incorporating STE into standard assessments may facilitate early interventions and enhance long-term cardiovascular outcomes for patients with RA.
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Dhahri et al. (2025) conducted a cross-sectional in Rheumatoid arthritis with normal left ventricular function (n=72). Rheumatoid arthritis vs. Healthy controls was evaluated on Global longitudinal strain (GLS) (p=0.015). Rheumatoid arthritis patients with normal left ventricular ejection fraction had significantly diminished global longitudinal strain compared to healthy controls (-18.99% vs -20.42%, p=0.015), indicating subclinical myocardial dysfunction.
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