Table 3.
Exophiala dermatitidis positive N = 31 | Exophiala dermatitidis negative N = 1281 | ||
---|---|---|---|
n (%) | n (%) | P-valueb | |
Demographic factors | |||
Age, years (mean, SD) | 28 (13) | 21 (14) | 0.005 |
Sex, female | 21 (68) | 607 (47) | 0.025 |
BMI, (mean, SD) | 22 (3) | 20 (4) | 0.003 |
Genotype, severe CFTR mutationsa | 27 (87) | 1005 (78) | 0.246 |
Disease characteristics | |||
CF-related diabetes | 6 (19) | 256 (21) | 1.000 |
ABPA | 4 (13) | 116 (9) | 0.529 |
Lung function, FEV1 (mean, SD) | 65 (19) | 71 (25) | 0.167 |
Microorganisms | |||
Pseudomonas aeruginosa | 11 (37) | 420 (36) | 0.950 |
Stenotrophomonas maltophilia | 3 (10) | 98 (8) | 0.733 |
Staphylococcus aureus | 10 (33) | 404 (34) | 0.926 |
Burkholderia cepacia | 1 (3) | 22 (2) | 0.442 |
Non-tuberculous mycobacteria | 1 (3) | 17 (1) | 0.364 |
Aspergillus spp. | 15 (50) | 314 (27) | 0.005 |
Medications | |||
Inhalation corticosteroids | 15 (48) | 330 (31) | 0.044 |
Azithromycin | 18 (58) | 512 (47) | 0.208 |
Inhalation antibiotics | 14 (45) | 483 (40) | 0.551 |
Severe mutations was defined as 2 CFTR mutations from class I-III.
T-test for continuous variables, Chi-2 for binary variables and Fisher's exact for binary variables with less than 10 cases.
BMI: body mass index, CFTR: Cystic fibrosis transmembrane conductance regulator, CF: Cystic fibrosis, ABPA: allergic bronchopulmonary aspergillosis, FEV1: forced expiratory volume in 1 second.