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Table 1 Baseline characteristics of patients with IPF according to the number of comorbidities at enrolment

From: Comorbidity burden and survival in patients with idiopathic pulmonary fibrosis: the EMPIRE registry study

 

Total

(N = 3580)

Number of comorbidities at enrolment

P-value a

0

(n = 310)

1

(n = 581)

2

(n = 670)

3

(n = 667)

 ≥ 4

(n = 1352)

Sex, n (%)

       

 Female

1050 (29.3)

93 (30.0)

168 (28.9)

226 (33.7)

203 (30.4)

360 (26.6)

0.022

 Male

2530 (70.7)

217 (70.0)

413 (71.1)

444 (66.3)

464 (69.6)

992 (73.4)

 

Age at enrolment, years (median, 5th; 95th percentile)

69 (53;82)

64 (45;78)

67 (51;82)

69 (53;82)

69 (55;81)

71 (58;83)

 < 0.001

Time from diagnosis to enrolment, months (median, 5th; 95th percentile)

0.46 (0.0;63.3)

0.49 (0.00;73.67)

0.03 (0.00;46.43)

0.56 (0.00;71.84)

0.69 (0.00;66.85)

0.56 (0.00;61.90)

 < 0.001

Median BMI, kg/m2 (5; 95 percentile)

28.0 (21.5;35.9)

26.6 (21.3;32.8)

27.5 (21.0;35.4)

27.8 (21.4;35.9)

28.4 (21.5;36.0)

28.4 (21.9;36.5)

 < 0.001

Smoking, n (%)

       

 Never-smoker

1353 (38.0)

137 (45.5)

254 (44.3)

261 (39.0)

248 (37.3)

453 (33.5)

 < 0.001

 Current smoker

169 (4.7)

18 (6.0)

31 (5.4)

31 (4.6)

34 (5.1)

55 (4.1)

 

 Ex-smoker

2039 (57.3)

146 (48.5)

289 (50.3)

377 (56.4)

383 (57.6)

844 (62.4)

 

Dyspnoea (NYHA categories, %)

       

 I

361 (10.7)

51 (19.0)

70 (13.2)

70 (11.1)

75 (11.8)

95 (7.2)

 < 0.001

 II

1762 (52.1)

152 (56.5)

303 (57.0)

347 (54.8)

321 (50.5)

639 (48.7)

 

 III

1183 (35.0)

63 (23.4)

151 (28.4)

194 (30.6)

226 (35.5)

549 (41.8)

 

 IV

77 (2.3)

3 (1.1)

8 (1.5)

22 (3.5)

14 (2.2)

30 (2.3)

 

HRCT, n (%)

       

 UIP

2297 (64.2)

195 (62.9)

374 (64.4)

445 (66.4)

426 (63.9)

857 (63.4)

0.864

 Possible UIP

862 (24.1)

75 (24.2)

148 (25.5)

155 (23.1)

162 (24.3)

322 (23.8)

 

 Inconsistent with UIP

127 (3.5)

10 (3.2)

21 (3.6)

22 (3.3)

24 (3.6)

50 (3.7)

 

 Not performed

294 (8.2)

30 (9.7)

38 (6.5)

48 (7.2)

55 (8.2)

123 (9.1)

 

Histopathology, n (%)

       

 UIP

418 (11.7)

57 (18.4)

74 (12.7)

90 (13.4)

65 (9.7)

132 (9.8)

0.009

 Probable UIP

143 (4.0)

16 (5.2)

25 (4.3)

31 (4.6)

25 (3.7)

46 (3.4)

 

 Possible UIP

119 (3.3)

10 (3.2)

18 (3.1)

24 (3.6)

20 (3.0)

47 (3.5)

 

 Not UIP

118 (3.3)

14 (4.5)

24 (4.1)

19 (2.8)

22 (3.3)

39 (2.9)

 

 Not performed

2782 (77.7)

213 (68.7)

440 (75.7)

506 (75.5)

535 (80.2)

1088 (80.5)

 

Antifibrotic treatment, n (%)

       

 Pirfenidone

1098 (30.6)

72 (23.2)

150 (25.8)

183 (27.3)

220 (33.0)

473 (35.0)

 < 0.001

 Nintedanib

917 (25.6)

99 (31.9)

169 (29.1)

187 (27.9)

153 (22.9)

309 (22.9)

 

 Switch pirfenidone to nintedanib

165 (4.6)

11 (3.5)

20 (3.4)

40 (6.0)

36 (5.4)

58 (4.3)

 

 Switch nintedanib to pirfenidone

77 (2.1)

7 (2.3)

12 (2.1)

12 (1.8)

10 (1.5)

36 (2.7)

 

 No antifibrotic treatment

1323 (37.0)

121 (39.0)

230 (39.6)

248 (37.0)

248 (37.2)

476 (35.2)

 

Lung function parameters, median (5; 95 percentile)

       

 FVC, % predicted

77 (45;114)

73 (43;112)

77 (49;116)

79 (47;117)

78 (45;112)

75 (44;112)

0.000

 FEV1, % predicted

81 (48;114)

79 (47;113)

83 (53;122)

82 (49;116)

81 (49;112)

79 (46;110)

0.000

 TLC, % predicted

47.4 (22.2;81.5)

48.0 (23.0;84.0)

48.4 (23.4;82.5)

49.4 (22.7;84.8)

48.2 (25.7;80.6)

45.1 (21.1;77.9)

0.001

 6MWD, m

391 (165;558)

450 (240;605)

420 (165;572)

393 (170;543)

398 (150;568)

370 (150;525)

0.000

  1. 6MWD 6-min walking distance, BMI body mass index, EMPIRE European Multipartner IPF REgistry, FEV1 forced expiratory volume in 1 s, FVC forced vital capacity, HRCT high-resolution computed tomography, IPF idiopathic pulmonary fibrosis, ML maximum likelihood, NYHA New York Heart Association functional classification, TLC total lung capacity, UIP usual interstitial pneumonia
  2. aStatistical significance tested by Kruskal–Wallis test for continuous parameters and by ML chi-square for categorical variables