Drs. Rajeev Saggar and Dinesh Khanna contributed equally to this work.
Exercise-induced pulmonary hypertension associated with systemic sclerosis: Four distinct entities
Version of Record online: 30 NOV 2010
Copyright © 2010 by the American College of Rheumatology
Arthritis & Rheumatism
Volume 62, Issue 12, pages 3741–3750, December 2010
How to Cite
Saggar, R., Khanna, D., Furst, D. E., Shapiro, S., Maranian, P., Belperio, J. A., Chauhan, N., Clements, P., Gorn, A., Weigt, S. S., Ross, D., Lynch, J. P. and Saggar, R. (2010), Exercise-induced pulmonary hypertension associated with systemic sclerosis: Four distinct entities. Arthritis & Rheumatism, 62: 3741–3750. doi: 10.1002/art.27695
- Issue online: 30 NOV 2010
- Version of Record online: 30 NOV 2010
- Accepted manuscript online: 18 AUG 2010 02:37PM EST
- Manuscript Accepted: 29 JUL 2010
- Manuscript Received: 20 JAN 2010
- NIH (National Institute of Arthritis and Musculoskeletal and Skin Diseases). Grant Number: K23-AR-053858-03
- Scleroderma Foundation (New Investigator Award)
Exercise-induced pulmonary hypertension (PH) may represent an early but clinically relevant phase in the spectrum of pulmonary vascular disease. There are limited data on the prevalence of exercise-induced PH determined by right heart catheterization in scleroderma spectrum disorders. We undertook this study to describe the hemodynamic response to exercise in a homogeneous population of patients with scleroderma spectrum disorders at risk of developing pulmonary vascular disease.
Patients with normal resting hemodynamics underwent supine lower extremity exercise testing. A classification and regression tree (CART) analysis was used to assess combinations of variables collected during resting right heart catheterization that best predicted abnormal exercise physiology, applicable to each individual subject.
Fifty-seven patients who had normal resting hemodynamics underwent subsequent exercise right heart catheterization. Four distinct hemodynamic groups were identified during exercise: a normal group, an exercise-induced pulmonary venous hypertension (ePVH) group, an exercise out of proportion PH (eoPH) group, and an exercise-induced PH (ePH) group. The eoPH and ePVH groups had higher pulmonary capillary wedge pressure (PCWP) than the ePH group (P < 0.05). The normal and ePH groups had exercise PCWP ≤18 mm Hg, which was lower than that in the ePVH and eoPH groups (P < 0.05). During submaximal exercise, the transpulmonary gradient and pulmonary vascular resistance (PVR) were elevated in the ePH and eoPH groups as compared with the normal and ePVH groups (P < 0.05). CART analysis suggested that resting mean pulmonary artery pressure (mPAP) ≥14 mm Hg and PVR ≥160 dynes/seconds/cm−5 were associated with eoPH and ePH (positive predictive value 89% for mPAP 14–20 mm Hg and 100% for mPAP >20 mm Hg).
We characterized the exercise hemodynamic response in at-risk patients with scleroderma spectrum disorders who did not have resting PH. Four distinct hemodynamic groups were identified during exercise. These groups may have potentially different prognoses and treatment options.