Diaphragmatic dysfunction and dyspnoea in amyotrophic lateral sclerosis

Amyotrophic lateral sclerosis (ALS) is a progressive disorder of unknown origin. Respiratory involvement is the principal cause of death, and dyspnoea is a major source of discomfort. In this study, diaphragm function is described and its relationship with dyspnoea examined in 48 ALS patients (32 male, age 26–80 yrs). The detailed neurological and respiratory evaluation (clinical examination, pulmonary function tests, static pressures, mouth twitch pressures (Pm,t), electromyographic responses to phrenic nerve stimulation and cortical magnetic stimulation were analysed after stratification according to dyspnoea. Dyspnoeic (group I) and nondyspnoeic (group II) patients were similar, bulbar signs being more frequent in group I. Vital capacity was lower in group I (mean±sd 67.9±22.7 versus 87.9±15.6% of the predicted value, p=0.0028), as were maximal static inspiratory pressure (41±24 versus 60±27% pred, p=0.0242) maximal static inspiratory pressure (18±11 versus 32±14% pred, p=0.0042), and Pm,t (3.71±2.5 versus 7.26±3.45 cmH2O, p=0.0011). Abdominal (Abd) paradox and respiratory pulse were frequent in group I (15 of 25 and 14 of 25) but absent or rare in group II (0 of 23 and four of 23) (p