Am. J. Respir. Crit. Care Med., Vol 153, No. 4, 04 1996, 1368-1376.
Lymphangioleiomyomatosis: the pathophysiology of diminished exercise capacity
RS Crausman, CA Jennings, RL Mortenson, LM Ackerson, CG Irvin and TE King Jr
Department of Medicine, National Jewish Center for Immunology and Respiratory Medicine, Denver, Colorado, USA.
Dyspnea with exertion is nearly always present in patients with pulmonary
lymphangioleiomyomatosis, but the mechanisms underlying exercise impairment
have not been well defined. Spirometry, lung volumes, lung mechanics, and
exercise physiology were performed on a cohort of 16 patients. We
determined the relative contribution of airflow limitation, gas exchange
abnormalities, and pulmonary vascular abnormalities to the exercise
performance achieved. The patients had normal TLC and Vtg, but RV was
elevated in 88% of the subjects. A moderate to severe obstructive pattern
was present in 69% of the subjects, and the DLCO was reduced, often
markedly, in 81% of the subjects. Exercise performance was limited (work
load, 68% +/- 6) with abnormalities of ventilatory function and gas
exchange present. Strong correlations between overall exercise performance
(percent predicted VO2max and maximal work load achieved) and indices of
airflow and vascular involvement were present. Poor exercise performance
was due primarily to ventilatory limitation. The etiology of this
ventilatory limitation appears twofold. First, subjects had a reduced
ventilatory ceiling because of airflow limitation. Second, subjects
demonstrated an excessive ventilatory response as a result of increased
dead-space ventilation thought to be due to disease-associated cystic
changes and associated pulmonary vascular dysfunction or destruction.
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Copyright © 1996 American Thoracic Society
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