Abstract
Background: Reduced exercise tolerance is a clear hallmark of cystic fibrosis (CF) and also an important prognostic factor. To date, it is not well established whether six-minute walk test (6MWT) and cardiopulmonary exercise test (CPET) provide similar sensitivity results in the assessment of exercise tolerance in adults with CF. Objective: The aim of the study was to compare 6MWT and CPET in the evaluation of exercise tolerance in CF adults with mild to moderate lung impairment. Methods: 30 stable CF adults (20 males, 10 females; age 32.9±8.8 years; FEV 1 70.2±19.1% predicted, BMI 22.6±2.7 kg/m 2 ) and 15 age-sex-BMI matched healthy controls (HC) were recruited. All participants underwent 6MWT and incremental CPET on cycle-ergometer: maximal distance at 6MWT (6MWD) and peak oxygen uptake (V9O 2 peak ) at CPET were measured, together with other physiologic variables. Lower limits of normal values (LLN) were calculated from the 5 th percentile of HC results’ distributions. Results: 6MWD was similar between CF patients and HC (656.3±65.5 vs 719.6±100.9 m, p =ns). By contrast, V9O 2 peak was significantly lower in CF patients, both as normalized for body weight (28.7±5.0 vs 38.1±4.2 ml/min/kg, p p 2 peak was found in 66.7% of them. 14 of 19 (73.7%) CF patients with normal 6MWD showed reduced exercise tolerance if assessed by V9O 2 peak . Conclusions: Despite of the advantage of being an easy test to perform, 6MWT is not as accurate and sensitive as CPET in detecting exercise intolerance in CF adults.
Published Version
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