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. 2021 Mar 7;10(3):585. doi: 10.3390/cells10030585

Table 1.

Demographics of study patients.

HC (n = 200) Sar (n = 215) HP (n = 30) (E)GPA (n = 11) IPF (n = 68)
Age a 46.6 ± 9.2 48.2 ± 11.8 59.6 ± 9.5 54.7 ± 13.9 69.5 ± 8.9
Sex (male) 92 (46) 117 (54) 15 (50) 7 (64) 60 (88)
Ethnicity (White) 190 (89) 30 (100) 11 (100) 67 (99)
Smoker (Never) 105 (49) 13 (43) 4 (36) 16 (24)
Immunosuppressive medication 0 101 (47) 12 (40) 6 (55) 0
CRP (mg/L) 2.0 IQR 4.0 2.0 IQR 4.0 2.0 IQR 23.0 3.5 IQR 5.0
FVC % predicted 94.3 ± 20.3 78.5 ± 21.7 90.0 ± 21.2 80.1 ± 20.1
FEV1 % predicted 84.9 ± 21.5 81.2 ± 22.0 86.2 ± 20.1 82.9 ± 18.3
DLCO % predicted 73.5 ± 17.4 46.8 ± 13.8 58.9 ± 20.2 41.5 ± 11.4
Scadding stage NA NA NA
0 44 (21)
I 45 (21)
II 50 (23)
III 32 (15)
IV 40 (19)
Unknown 4 (2)

Values are shown as absolute numbers with percentages in brackets; a Age, FVC % predicted, FEV1 % predicted and DLCO % predicted are shown as mean ± std. CRP, is shown as median IQR.; Medication consisted of immunosuppressive medication including prednisone, methotrexate, azathioprine, infliximab, leflunomide, adalumimab, hydroxychloroquine and cellcept.; CRP was available from 207 sarcoidosis patients, 27 HP patients, 9 (E)GPA patients and 68 IPF patients.; FVC was available from 166 sarcoidosis patients, 27 HP patients, 11 (E)GPA patients and 59 IPF patients; FEV1 was available from 174 sarcoidosis patients, 26 HP patients, 11 (E)GPA patients and 60 IPF patents; DLCO was available from 160 sarcoidosis patients, 25 HP patients, 7 (E)GPA patients and 55 IPF patients; HC: healthy control, Sar: sarcoidosis, HP: hypersensitivity pneumonitis, (E)GPA: (eosinophilic) granulomatosis with polyangiitis ((E)GPA), IPF: idiopathic pulmonary fibrosis, CRP: C-reactive protein, FVC: Forced vital capacity, FEV1: Forced expiratory volume in 1 s, DLCO: Diffusing capacity.