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Primary antiphospholipid syndrome as a cause of impaired left ventricular diastolic function: experience from a
Aleksandra Djokovic1, Ljudmila Stojanovich2, Natasa Stanisavljevic3
1University of Belgrade, Faculty of Medicine, Belgrade; and Department of Cardiology, University Hospital Center Bezanijska Kosa, Belgrade, Serbia. drsaska@yahoo.com.
Insights
Patients with antiphospholipid syndrome (APS) show higher rates of left ventricular diastolic dysfunction (LVDD). Thrombosis in APS is a key predictor of LVDD, highlighting the need for managing cardiovascular risk factors.
Area of Science:
- Cardiology
- Rheumatology
- Internal Medicine
Background:
- Antiphospholipid syndrome (APS) can cause cardiovascular issues through acquired thrombophilia and accelerated atherosclerosis.
- Assessing left ventricular diastolic performance offers early insight into myocardial involvement in primary APS (PAPS).
Purpose of the Study:
- To evaluate left ventricular diastolic function in patients with primary antiphospholipid syndrome (PAPS).
- To identify early signs of myocardial involvement in PAPS.
Main Methods:
- Analyzed 101 PAPS patients and 90 healthy controls.
- Assessed anticardiolipin antibodies (aCL IgG/IgM), anti-ß2 glycoprotein-I (anti-ß2GPI IgG/IgM), and lupus anticoagulant (LAC).
- Defined left ventricular diastolic dysfunction (LVDD) based on echocardiographic parameters (e.g., E´ velocity, E/E´ ratio, LAVI, TRV).
Main Results:
- LVDD was significantly more prevalent in PAPS patients (24.8%) than controls (2.2%).
- LVDD in PAPS was linked to age, BMI, hyperlipidemia, thromboses, and LAC positivity.
- PAPS patients exhibited higher LAVI and isovolumic relaxation time, with lower lateral E´ velocity and E/E´ ratio compared to controls.
- Multivariate analysis identified thromboses as an independent predictor of LVDD in PAPS.
Conclusions:
- Thrombotic PAPS patients face an elevated risk of developing LVDD.
- Aggressive management of atherosclerotic risk factors and appropriate therapies are vital for preserving left ventricular diastolic function in PAPS.
Objectives:
Cardiovascular manifestations, encountered in antiphospholipid syndrome, may develop as a consequence of acquired thrombophilia mediated by antiphospholipid antibodies and accelerated atherosclerosis as well. Our study aims to assess the impairment of the left ventricular diastolic performance, as early evidence of myocardial involvement in primary antiphospholipid syndrome (PAPS).
Methods:
We analysed 101 PAPS patients, with the average age of 47.70±13.14y. Anticardiolipin antibodies (aCL IgG/IgM), anti-ß2 glycoprotein-I (anti-ß2GPI IgG/IgM), and lupus anticoagulant (LAC) were determined. Abnormal cut-off values used for left ventricular diastolic dysfunction (LVDD) were septal E ́<7 cm/sec, lateral E ́ <10 cm/sec, average E/E ́ ratio >14, LA volume index (LAVI) >34 mL/m2, and peak tricuspid regurgitation velocity >2.8 m/sec. LVDD was present if more than half parameters were with abnormal values. The results were compared to 90 healthy, age and sex-matched controls.
Results:
LVDD was significantly more prevalent in PAPS patients compared to healthy controls (24.8% vs. 2.2%, p=0.001). In PAPS patients, it was signi cantly related to age, body mass index, hyperlipidaemia, thromboses and LAC positivity (p=0.0001, p=0.008, p=0.039, p=0.001, p=0.047 respectively). Patients with PAPS had higher LAVI (29.76±6.40 ml/m2 vs. 26.62±7.8 ml/m2, p=0.012), higher isovolumic relaxation time, lower lateral É velocity and lower E/É ratio compared to controls (p=0.0001, p=0.020, p=0.038, respectively). In multivariate analysis, thromboses in PAPS were significant, and independent predictors of LVDD.
Conclusions:
Thrombotic PAPS patients are at higher risk of LVDD development. Strong action against standard atherosclerotic risk factors and adequate therapy regimes seems to be crucial to preserve good diastolic performance of the left ventricle in PAPS.
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