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. 2020 Nov 26;9(12):3828. doi: 10.3390/jcm9123828

Table 1.

Demographic characteristics of the study cohort.

Variable Without PH With PH Severe PH p-Value
(n = 188) (n = 96) (n = 56)
Age 55.8 ± 15.6 60.2 ± 14.3 59.3 ± 14.3 0.042
Male sex 93 (49.5) 36 (37.5) 25 (44.6) 0.158
Ever smoker 46 (24.4) 17 (17.7) 17 (30.3) 0.187
Follow-up duration, months 42.7 ± 38.5 40.8 ± 37.8 41.7 ± 37.5 0.921
BMI, kg/m2 28.9 ± 6.3 30.1 ± 6.6 30.4 ± 8.4 0.202
Underlying disease
IPF 59 (31.3) 34 (35.4) 22 (39.2) 0.508
CTD-ILD 70 (37.2) 39 (40.6) 20 (35.7) 0.798
Rheumatoid arthritis 13 (6.9) 4 (4.1) 1 (1.7) 0.272
SLE 5 (2.6) 3 (3.1) 1 (1.7) 0.884
Systemic sclerosis 8 (4.2) 9 (9.3) 0 0.030
Primary Sjogren’s syndrome 10 (5.3) 13 (13.5) 7 (12.5) 0.039
Polymyositis 3 (1.5) 0 1 (1.7) 0.448
MCTD 11 (5.8) 2 (2.0) 2 (3.5) 0.324
UCTD 20 (10.6) 8 (8.3) 8 (14.2) 0.516
Sarcoidosis 26 (13.8) 11 (11.4) 11 (19.6) 0.371
Chronic Hypersensitivity Pneumonitis 14 (7.4) 5 (5.2) 1 (1.7) 0.272
Idiopathic NSIP 4 (2.1) 4 (4.1) 2 (3.5) 0.601
Others
Organizing Pneumonia 4 (2.1) 2 (2.0) 0 0.547
Unclassifiable fibrosis 6 (3.1) 0 0 0.085
RBILD 3 (1.5) 1 (1.0) 0 0.617
DIP 2 (1.0) 0 0 0.443

Data are presented as the means ± standard deviations or numbers (percentages). PH: pulmonary hypertension; BMI: body mass index; IPF: idiopathic pulmonary fibrosis; CTD: connective tissue disease; ILD: interstitial lung disease; SLE: systemic lupus erythematosus; MCMCTD: mixed connective tissue disease; UCTD: undifferentiated connective tissue disease; NSIP: nonspecific interstitial pneumonia; RBILD: respiratory bronchiolitis interstitial lung disease; DIP: desquamative interstitial pneumonia.