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Value of Speckle Tracking Echocardiography for Early Detection of Left Ventricular Dysfunction in Patients with Systemic Lupus Erythematosus

Journal of Cardiovascular Echography • 2020
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Publication Information
Authors Shereen Ibrahim Farag, Reda Biomy Bastawisy, Mohamed Ahmed Hamouda, Wael Anwer Hassib, Hala Ahmed Wahdan
Keywords Speckle tracking echocardiography, systemic lupus erythematosus, ventricular function
Journal Journal of Cardiovascular Echography
Publisher Not Available
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publication.type International
Paper Link Not Available
Supplementary Materials Not Available
Abstract
Background: Cardiac dysfunction due to systemic lupus erythematosus (SLE) may be subclinical, but those patients are at high risk for
developing clinical heart failure. Aim: The aim of this study is to assess the role of speckle tracking echocardiography (STE) in the early detection
of systolic dysfunction in SLE patients. Patients and Methods: This was a case–control study. Participants were subdivided into two groups:
Group 1 included 50 SLE patients and Group 2 included 50 healthy controls. Clinical evaluation, echocardiography, tissue Doppler, and STE
were performed. Results: Global longitudinal strain (GLS) was significantly reduced in SLE group (−18.95 ± 2.02 vs. −21.4 ± 2.1, P < 0.001).
However, there was no significant difference in left ventricular ejection fraction between both groups (P = 0.801). There was a significant positive
correlation between the disease duration and age (r = 0.480, P < 0.001), pulmonary artery systolic pressure (PASP) (r = 0.628, P < 0.001),
and GLS (%) (r = 0.417, P = 0.012). There was also a significant positive correlation between the disease activity index and GLS (%)
(r = 0.7, P < 0.001) and PASP (r = 0.522, P < 0.001). Conclusion: SLE group had GLS % lower than the control group, and this was statistically
significant, denoting early systolic dysfunction. Longer duration and high SLE activity index significantly affect GLS. GLS is an excellent
noninvasive tool for early detection of subclinical left ventricular systolic dysfunction in SLE patients.