Table 1 Pilot cohort to assess the stability of serum CC-16 as a biomarker for COPD
COPD subjects(n = 195)Smoker controls(n = 36)Non-smoker controls(n = 36)p Value†
Age64.5 (6.0)60.8 (7.7)59.7 (8.8)0.002
Male (%)141 (72)24 (67)14 (39)0.492
Smoking history (pack-years)45.8 (27.2)29.8 (16.5)1 (0)<0.001
FEV1 (l)1.2 (0.5)3.2 (0.6)3.1 (0.7)<0.001
FEV1 (% pred)43.9 (16.9)108.9 (11.8)115.8 (12.0)<0.001
FEV1/FVC0.40 (0.12)0.80 (0.06)0.80 (0.05)<0.001
CT scans (n)*1782932
% Low attenuation area (<−950 HU)22.6 (13.5)4.5 (4.4)5.4 (5.5)<0.001
Baseline CC-16 (ng/ml), median (IQR)5.9 (3.9)6.3 (2.3)7.5 (4.3)0.117
Number of CC-16 results at 3 months1823534
3 month CC-16 (ng/ml), median (IQR)5.7 (3.6)6.6 (3.3)8.2 (4.3)0.046
  • All values are number or mean and standard deviation (in brackets) unless otherwise stated.

  • The lung function measurements were performed following the administration of 180 μg salbutamol. All the smoking controls and individuals with COPD were former smokers.

  • *CT scans is the number of CT scans available for qualitative analysis to assess the percentage of the lungs with a density of less than −950 HU.

  • †p values for difference between COPD subjects and smoker controls. All the parameters measured were significantly different between individuals with COPD and non-smoker controls (p⩽0.005).

  • CC-16, Clara cell secretory protein-16; COPD, chronic obstructive pulmonary disease; FEV1, forced expiratory volume in 1 s; FVC, forced vital capacity; IQR, interquartile range.