Myocardial left ventricular dysfunction in patients with systemic lupus erythematosus: new insights from tissue
Sebastian J Buss1, David Wolf, Grigorios Korosoglou
1Department of Cardiology, Angiology and Pulmology, University of Heidelberg, Im Neuenheimer Feld 410, 69120 Heidelberg, Germany. sebastian.buss@med.uni-heidelberg.de
Insights
Systemic lupus erythematosus (SLE) patients show impaired left ventricular (LV) function on advanced echocardiography, even without symptoms. New imaging techniques detect subclinical heart disease in SLE earlier than standard methods.
Area of Science:
- Cardiology
- Rheumatology
- Medical Imaging
Background:
- Systemic lupus erythematosus (SLE) significantly increases cardiovascular morbidity and mortality.
- Routine imaging often underestimates cardiovascular involvement in SLE patients.
- Early detection of cardiac dysfunction is crucial for managing SLE patients.
Purpose of the Study:
- To evaluate novel echocardiographic techniques, including tissue Doppler (TDI), strain rate (SRR), and strain (SRI) imaging.
- To detect subclinical left ventricular (LV) dysfunction in asymptomatic SLE patients.
- To compare the efficacy of new imaging modalities against standard echocardiography in SLE.
Main Methods:
- Sixty-seven SLE patients and 40 healthy controls underwent standard echocardiography, TDI, SRR, and SRI.
- Patients were assessed for symptoms of heart failure or angina.
- Disease activity was quantified using ECLAM and SLEDAI scores.
Main Results:
- Despite normal standard echocardiograms, SLE patients exhibited impaired LV systolic and diastolic function via TDI, SRR, and SRI compared to controls.
- Elevated SLE disease activity correlated with reduced LV longitudinal function measured by SRR and SRI.
- Newer imaging modalities revealed significant subclinical myocardial abnormalities in SLE patients.
Conclusions:
- Systemic lupus erythematosus is linked to significant subclinical impairment of LV longitudinal function.
- Advanced echocardiographic techniques like TDI, SRR, and SRI are superior to standard methods for detecting early cardiac involvement in SLE.
- These findings highlight the importance of advanced imaging for proactive cardiovascular risk management in SLE.
Objective:
Systemic lupus erythematosus (SLE) is associated with high cardiovascular morbidity and mortality. Cardiovascular involvement is frequently underestimated by routine imaging techniques. Our aim was to determine if new echocardiographic imaging modalities like tissue Doppler (TDI), strain rate (SRR), and strain (SRI) imaging detect abnormalities in left ventricular (LV) function in asymptomatic patients with SLE.
Methods:
Sixty-seven young patients with SLE (mean age 42 +/- 10 yrs) without typical symptoms or signs of heart failure or angina, and a matched healthy control group (n = 40), underwent standard transthoracic echocardiography, TDI, SRR, and SRI imaging of the LV as well as assessment of disease characteristics.
Results:
Despite findings within the normal range on routine standard 2-dimensional echocardiography, SLE was associated with significantly impaired systolic and diastolic myocardial velocities of the LV measured by TDI [mean global TDI: systolic (s): 2.9 +/- 0.9 vs 3.9 +/- 0.7 cm/s, p < 0.05; early (e): 4.3 +/- 1.5 vs 6.3 +/- 1.3 cm/s, p < 0.05; late (a): 2.9 +/- 0.8 vs 3.4 +/- 0.8 cm/s, p < 0.05; values +/- SD); SRR (s: -0.8 +/- 0.1 vs -1.1 +/- 0.1 s(-1); e: 1.1 +/- 0.2 vs 1.6 +/- 0.3 s(-1); a: 0.7 +/- 0.1 vs 1.0 +/- 0.2 s(-1); all p < 0.05); and SR (-15.11 +/- 2.2% vs -19.7 +/- 1.9%; p < 0.05) compared to the control group. Further, elevated disease activity, measured with the ECLAM and the SLEDAI score, resulted in significantly lower values for LV longitudinal function measured by SRR and SR, but not by TDI.
Conclusion:
SLE is associated with a significant impairment of systolic and diastolic LV longitudinal function in patients without cardiac symptoms. New imaging modalities provide earlier insight into cardiovascular involvement in SLE and seem to be superior to standard echocardiography to detect subclinical myocardial disease.
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