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. 2015 May 15;191(10):1116–1125. doi: 10.1164/rccm.201408-1440OC

Table 2.

Pulmonary Function of TEA Clusters in YCAAD Cohort

  Control Subjects (n = 12) Cluster 1 (n = 34) Cluster 2 (n = 19) Cluster 3 (n = 47) P Value
FEV1, % of predicted value
 Pre–β2-agonist use 96 ± 11 73 ± 24 76 ± 22 86 ± 22 0.006
 Post–β2-agonist use 98 ± 14 80 ± 24 81 ± 20 91 ± 22 0.493
FVC, % of predicted value
 Pre–β2-agonist use 86 ± 22 85 ± 22 86 ± 18 96 ± 19 0.09
 Post–β2-agonist use 91 ± 20 90 ± 20 88 ± 18 97 ± 18 0.28
FEV1/FVC
 Pre–β2-agonist use 0.77 ± 0.62 0.67 ± 0.13 0.70 ± 0.11 0.72 ± 0.10 0.13
 Post–β2-agonist use 0.79 ± 0.50 0.70 ± 0.13 0.72 ± 0.12 0.80 ± 0.10 0.06
BDR, % 2 ± 6.2 12 ± 12 9 ± 13 6 ± 7 0.03
FeNO, ppb 20 ± 9.7 53 ± 43 52 ± 42 38 ± 27 0.04

Definition of abbreviations: BDR = bronchodilator response; FeNO = exhaled nitric oxide; TEA = transcriptomic endotypes of asthma; YCAAD = Yale Center for Asthma and Airway Diseases.

Data are means ± SD. P values for comparisons among TEA clusters were determined using Kruskal-Wallis or Cochran-Armitage test. The false discovery rate estimated by the permutation-based method is 5.6%.