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Table 1 Sample characteristics stratified by clusters

From: Lung clearance index to characterize clinical phenotypes of children and adolescents with cystic fibrosis

 

Total

Cluster #1

Cluster #2

P-value

Subjects, nr

125

78

47

 

Age, years

11.4 (2.8)

11.1 (3)

11.8 (2.3)

0.156

Sex, female

61 (48.8)

36 (46.2)

25 (53.2)

0.466

BMI Z score

− 0.57 (0.88)

− 0.68 (0.78)

− 0.37 (1.00)

0.073

Pancreatic insufficiency

74 (59.2)

74 (94.9)

< 0.001

CFRD

1 (0.8)

1 (1.3)

1.000

CFTR genotype

< 0.001

 F508del/other

50 (40.0)

32 (41.0)

18 (38.3)

 

 F508del/F508del

31 (24.8)

30 (38.5)

1 (2.1)

 

 Other/other

44 (35.2)

16 (20.5)

28 (59.6)

 

Pseudomonas aeruginosa, free

76 (65)

41 (52.6)

35 (85.4)

< 0.001

FEV1% predicted

100.4 (17.4)

95.3 (18.0)

109.0 (12.4)

< 0.001

FEV1 Z score

0.05 (1.48)

− 0.38 (1.52)

0.79 (1.08)

< 0.001

FVC % predicted

107.4 (14.7)

104.4 (16.0)

112.4 (10.7)

0.002

FVC Z score

0.61 (1.23)

0.35 (1.34)

1.03 (0.90)

0.001

LCI

10.07 (2.98)

11.33 (2.91)

7.97 (1.57)

< 0.001

LCI Z score, median (IQR)

5.22 (7.89)

8.32 (8.44)

0.98 (2.98)

< 0.001

Sacin*VT

0.138 (0.109)

0.161 (0.116)

0.1 (0.084)

0.001

Scond*VT

0.066 (0.030)

0.078 (0.024)

0.045 (0.028)

< 0.001

Pulmonary exacerbationsa, median (IQR)

2 (0–3)

3 (1–4)

0 (0–1)

< 0.001

Hospitalizationa

< 0.001

 1

15 (12.0)

15 (19.2)

 

2

4 (3.2)

4 (5.1)

 
  1. Values are expressed as absolute number (percentage) or mean (sd), where not differently expressed
  2. CFTR cystic fibrosis transmembrane conductance regulator
  3. aReference time period is 12 months preceding first MBWN2 test