M. Karetzky et M. Mcdonough, EXERCISE AND RESTING PULMONARY-FUNCTION IN SARCOIDOSIS, Sarcoidosis vasculitis and diffuse lung diseases, 13(1), 1996, pp. 43-49
Patients with sarcoidosis frequently complain of exercise intolerance
but reports of the value of static tests of pulmonary function in pred
icting disability have been contradictory. We studied 32 patients with
sarcoidosis and dyspnea, correlating x-ray stages, spirometry and lun
g volume measurements with graded exercise testing. Patients demonstra
ted a reduction in maximum workload (Wmax) when compared to an age mat
ched group of 7 normal subjects (p<0.05). While ventilation (VEmax) at
Wmax was lower in patients, when adjusted for workload (V/E/watt) the
re was relative hyperventilation (p<0.05). Exercise induced arterial d
esaturation (PaO2 decrease) was significantly related to resting DLCO%
predicted (r=0.74, p<0.05). When patients were separated into subgrou
ps of> < DLCO 55% predicted, the lower diffusing capacity group had a
lower Wmax and greater fall in exercise PaO2. Chest radiograph staging
and the vital capacity proved to be poor predictors of exercise capac
ity though maximum impairment was associated with advanced x-ray chang
es and greater decreases in vital capacity. In conclusion, the magnitu
de of functional impairment may vary widely from apparent histopatholo
gic involvement as reflected by chest x-ray and lung volumes. Actual e
xercise testing is necessary to accurately characterize and quantitate
the impairment in patients with sarcoidosis complaining of dyspnea.