TABLE 2

Comparison of clinical characteristics and different clusters’ PEF measurements

Cluster 1 (n=12)Cluster 2 (n=20)Cluster 3 (n=12)Unclustered (n=61)p-value
Subjects n12201261
Male sex8 (67)11 (55)8 (67)43 (70)0.86
Age years13.8 (8–17)12.2 (5–16)11.8 (7–16)12.4 (6–17)0.49
BMI20 (15–30)20 (15–32)19.5 (14–27)20 (14–39)0.73
BMI centile67.5 (9–99)68 (19–97)65 (6–98)72 (0–100)0.71
Ethnicity: white/other %67/3360/4067/3348/520.46
Comorbidity5 (42)2 (10)2 (17)10 (16)0.14
Median age of symptom onset months15.5 (1–84)18.0 (1–132)9.5 (1–72)12 (1–120)0.53
Hospitalisations n0 (0–3)0 (0–5)0 (0–5)0 (0–15)0.97
Atopic subjects10 (83)15 (75)11 (92)56 (92)0.23
LTRA5 (42)12 (60)5 (42)39 (64)0.32
Maintenance OCS2 (17)1 (5)1 (8)4 (7)0.64
Omalizumab001 (8)3 (5)0.57
FEV1 % pred (BL)71.1± 18.4294.1± 17.8892.3± 11.6885.2±18.560.0057#
FEV1 % pred (FU)83.9±15.3197.3±17.61102.3±10.2389.9±15.210.0085

Data are presented as n (%), median (range) or mean±sd, unless otherwise stated. BL: baseline; FU: follow-up; BMI: body mass index; LTRA: leukotriene receptor antagonists; ICS: inhaled corticosteroids; OCS: oral corticosteroids; FVC: forced vital capacity; FEV1: forced expiratory volume in 1 s. #: Bonferroni post-test (Holm–Sidak's multiple comparisons test): significant difference between cluster 1 versus 3, cluster 1 versus 2, cluster 1 versus unclustered; : Bonferroni post-test (Holm–Sidak's multiple comparisons test) FU: only cluster 1 versus 3. Comorbidities were migraine, focal epilepsy and delayed puberty. Bold text indicates statistical significance (p<0.05).