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Table 1 Patient demographics

From: CFTR regulates B cell activation and lymphoid follicle development

 

Cystic fibrosis (n = 27)

Controls (n = 10)

p value

Age (yr)

15.9 ± 0.98

15.3 ± 0.65

0.71

Sex (M/F)

15/12

5/5

0.77

Race or ethnic group (no.)

  Caucasian

25

  

  Hispanic

1

  

  Native American

1

  

Body-mass index (kg/m2)

18.1 ± 2.2

  

Prebronchodilator FEV1 (% of predicted value)

33.0 ± 0.04

  

Pancreatic insufficiency (no.)

27/27

  

Airway colonization with:

 Pseudomonas aeruginosa

19/25

  

 Methicillin-resistant Staphylococcus aureus

8/25

  

 Methicillin-sensitive Staphylocccus aureus

9/25

  

 Burkholderia cepacia complex

6/25

  

 Stenotrophomonas maltophilia

7/25

  

 Escherichia coli

3/25

  

 Enterobacter species

1/25

  

 Klebsiella species

1/25

  

 Other Staphylococcus species

1/25

  

CFTR genotype

  Homozygous F508del-CFTR

14

  

  Heterozygous F508del-CFTR

4

  

  Heterozygous other

1

  

  Unknown

8

  

Pancreatic insufficiency (no.)

27/27

  

CF-related diabetes mellitus (no.)

13/27

  

CF-related liver disease (no.)

5/27

  

Non-tuberculous mycobacteria lung infection (no.)

1/21

  

Allergic bronchopulmonary aspergillosis (no.)

4/27

  

Immunoglobulin E (mg/dL)

278 ± 107.5

  
  1. Plus-minus values indicate ± SEM
  2. CF cystic fibrosis, CFTR cystic fibrosis transmembrane conductance regulator, F508del-CFTR delta 508 CFTR mutation, FEV1 forced expiratory volume in 1 s