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a Department of
Pathophysiology, University of Athens, School of Medicine, Athens,
Greece, b Clinical and Molecular Epidemiology Unit,
Department of Hygiene and Epidemiology, University of Ioannina School
of Medicine, Ioannina, Greece, c Department of Cardiology, Laikon General
Hospital, Athens, Greece
Correspondence to: Professor H M Moutsopoulos, Department of Pathophysiology, Medical School, National University of Athens, 75 M Asias St, 115 27 Athens, Greece hmoutsop{at}dh.uoa.gr
Accepted for publication 5 June 2000
OBJECTIVE
To evaluate
the prevalence of diastolic dysfunction in patients
with anticardiolipin antibodies (aCL) and to examine whether the
antiphospholipid syndrome (APS) is associated with diastolic dysfunction independently of valvular abnormalities and systolic dysfunction.
METHODS
Pulsed,
continuous, colour Doppler echocardiography was performed in 179 subjects, of whom 15 were excluded from the analysis because of
systolic dysfunction or severe valvular disease. The remaining 164 subjects included 29 patients with primary APS, 26 patients with
secondary APS (APS in the presence of systemic lupus erythematosus
(SLE)), and 30 patients with SLE and aCL but without APS; 43 patients
with SLE without aCL and 36 normal volunteers served as control groups.
RESULTS
The groups
compared differed significantly in all measures of right ventricular
function. There was a gradation of increasing diastolic function
impairment as manifested by prolonged deceleration time (DT) and
isovolumic relaxation time (IVRT) across the groups of patients with
SLE without aCL, SLE with aCL, secondary APS, and primary APS.
Differences in left ventricular diastolic function measures were less
prominent. In regression analysis, DT increased by 19.6 ms (p=0.002) in
the presence of primary APS and by 20.1 ms (p=0.038) in the presence of
pulmonary hypertension. The titre of IgG aCL was the strongest
predictor of a prolonged IVRT.
CONCLUSION
Diastolic
dysfunction, in particular of the right ventricle
that is, independent
of valvular disease and systolic dysfunction, is a prominent feature of
APS and may be related to the pathogenesis of the syndrome.
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