Respiratory impairments in patients suffering from Fabry disease - A cross-sectional study

BackgroundThe inherited X-linked disorder, Fabry disease, is caused by deficient lysosomal enzyme alpha-galactosidase A, with progressive accumulation of globotriaosylceramide in multiple organs including the upper and lower airways. ObjectivesTo assess pulmonary function at the time of the first pulmonary function test (PFT) performed among the National Danish Fabry cohort and define the prevalence of affected lung function variables. Materials and MethodA cross-sectional retrospective cohort study of 86 adult patients enrolled in one or both international patient registry databases for Fabry disease, Fabry Registry or FollowME with at least one PFT. The Mainz Severity Score Index (MSSI) was calculated to determine the disease severity. Lung function variables were examined by multivariate regression adjusted for important variables for developing airway illness. ResultsSeventeen patients (20%) showed obstructive airflow limitation and 7 (8%) a restrictive lung deficiency. Smoking status (p = .016) and MSSI (p < .001) were associated with increasing obstructive airway limitation. ConclusionThe prevalence of affected lung function among the National Danish Fabry cohort was 28%. Patients with classic gene variants frequently developed a decrease in lung function regardless of their smoking status, with significant relationship with disease severity.