Five-year follow-up study of the prevalence and progression of pulmonary hypertension in systemic lupus erythematosus

• Published in: The American heart journal Vol. 129; no. 3; pp. 510 - 515
• Main Authors: Winslow, Timothy M., Ossipov, Maxim A., Fazio, Gary P., Simonson, Jay S., Redberg, Rita F., Schiller, Nelson B.
• Format: Journal Article
• Language: English
• Published: New York, NY Mosby, Inc 1995; Elsevier
• Subjects: Adult; Aged; Biological and medical sciences; Disease Progression; Echocardiography, Doppler; Female; Follow-Up Studies; Humans; Hypertension, Pulmonary - diagnostic imaging; Hypertension, Pulmonary - etiology; Hypertension, Pulmonary - physiopathology; Lupus Erythematosus, Systemic - complications; Lupus Erythematosus, Systemic - physiopathology; Male; Medical sciences; Middle Aged; Pneumology; Prevalence; Pulmonary hypertension. Acute cor pulmonale. Pulmonary embolism. Pulmonary vascular diseases; Tricuspid Valve Insufficiency - complications; Tricuspid Valve Insufficiency - diagnostic imaging; Vascular Resistance; Immunopathology; Connective tissue disease; Skin disease; Prevalence; Respiratory disease; Cardiovascular disease; Autoimmune disease; Pulmonary hypertension; Follow up study; Systemic disease; Evolution; Lupus erythematosus; Disseminated
• ISSN: 0002-8703; 1097-6744
• DOI: 10.1016/0002-8703(95)90278-3

The purpose of this study was to determine the prevalence and progression of pulmonary hypertension over a 5-year follow-up period in 28 patients with systemic lupus erythematosus (SLE) who were originally enrolled in an echocardiographic study of pulmonary hypertension in 1985 and 1986. Twenty healthy volunteers without cardiac or pulmonary disease participated as normal controls. Each patient and control underwent a complete Doppler echocardiographic study. Doppler echocardiographic recordings of tricuspid insufficiency, with saline contrast enhancement when necessary, were used to calculate pulmonary artery systolic pressure according to the modified Bemoulli equation. Doppler echocardiographic measurement of cardiac output was performed at rest for each subject, and pulmonary resistance was calculated by dividing the pulmonary artery systolic pressure by the cardiac output. These results were compared to results of the original studies to detect serial changes in pulmonary pressure and pulmonary resistance; results were also compared to the group of normal controls. The prevalence of pulmonary hypertension increased from 14% of the first study to 43% at follow-up. A significant increase in mean systolic pulmonary artery pressure wa detected in the SLE patients during the follow-up period: 23.4 vs 27.5 mm Hg ( p < 0.005). In addition, a significantly higher pulmonary artery pressure was detected in the SLE patients compared with the normal controls ( p < 0.005). An increase in pulmonary resistance during the follow-up period was detected for the SLE group as a whole ( p < 0.001) and for the subgroup of patients with pulmonary hypertension at the second study (p < 0.001), implying that the mechanism for pulmonary hypertension is common in SLE, is gradually progressive over time, and is related to an increase in pulmonary resistance.