Table 2

Patient characteristics of the three clusters identified in the final model

Patient characteristicsCluster 1
eosinophils >2.4%
(N=1777)
Cluster 2
Eosinophils ≤2.4%, pack-years ≤46
(N=891)
Cluster 3
eosinophils ≤2.4%, pack-years >46
(N=587)
p Value
Age, years65 (58–70)62 (55–69)65 (60–71)<0.0001
Female693 (39.0)480 (53.9)212 (36.1)<0.0001
Hispanic or Latino298 (16.8)192 (21.5)94 (16.0)0.0041
Current smoker714 (40.2)443 (49.7)282 (48.0)<0.0001
Number of pack-years40 (28–58)30 (20–39)61 (51–80)<0.0001
History of
 Cardiovascular disease1108 (62.4)519 (58.2)382 (65.1)0.0219
 Cardiac disorders306 (17.2)113 (12.7)107 (18.2)0.0036
 Coronary artery disease186 (10.5)65 (7.3)73 (12.4)0.0031
 Myocardial infarction104 (5.9)26 (2.9)35 (6.0)0.0027
 Eye disorders225 (12.7)87 (9.8)95 (16.2)0.0012
 Metabolism disorders729 (41.0)321 (36.0)244 (41.6)0.0277
Medication use
 Antithrombotic agents486 (27.3)178 (20.0)167 (28.4)<0.0001
 Antihypertensives87 (4.9)27 (3.0)35 (6.0)0.0195
 Lipid-modifying agents517 (29.1)187 (21.0)177 (30.2)<0.0001
 Anti-inflammatory and antirheumatic products643 (36.2)242 (27.2)209 (35.6)<0.0001
 Antihistamines for systemic use216 (12.2)73 (8.2)54 (9.2)0.0036
Exacerbations treated with steroid/antibiotics in the 12 months before screening visit
 0129 (7.3)67 (7.5)54 (9.2)0.47
 11104 (62.4)547 (61.4)341 (58.1).
 2363 (20.4)194 (21.8)136 (23.2).
 ≥3181 (10.2)83 (9.3)56 (9.5).
Number of hospitalised exacerbations in the 12 months before screening visit
 01428 (80.4)696 (78.1)469 (79.9)0.1044
 1291 (16.4)152 (17.1)104 (17.7).
 ≥258 (3.3)43 (4.8)14 (2.4).
COPD type
 Bronchitis1156 (65.4)634 (71.2)366 (62.8)0.0012
 Emphysema1021 (57.8)426 (47.9)362 (62.1)<0.0001
Baseline WBC, GI/L6.90 (5.80–8.10)7.20 (6.10–8.60)7.40 (6.20–8.90)<0.0001
Baseline lymphocytes, %27.30 (22.30–33.00)25.80 (21.10–31.30)25.30 (19.70–30.10)<0.0001
Baseline eosinophils, GI/L0.28 (0.21–0.39)0.11 (0.07–0.14)0.11 (0.07–0.15)<0.0001
Baseline eosinophils, %4.00 (3.10–5.60)1.50 (1.00–2.00)1.50 (1.00–2.00)<0.0001
Baseline eosinophils ≥2%1700 (100)233 (26.2)158 (26.9)<0.0001
Baseline neutrophils, %61.10 (55.10–66.70)66.40 (60.60–71.50)67.10 (62.10–72.70)<0.0001
Baseline neutrophils, GI/L4.19 (3.37–5.11)4.81 (3.81–5.98)4.99 (3.85–6.27)<0.0001
Baseline haemoglobin, G/L145.0 (136.0–153.0)145.0 (136.0–154.0)147.0 (138.0–156.0)0.0025
Baseline urea/BUN, mmol/L5.50 (4.50–7.00)5.20 (4.20–6.50)5.45 (4.50–6.50)0.0024
Lung function at screening
 Pre-bronchodilator FEV1, L1.10 (0.81–1.41)1.12 (0.81–1.42)1.02 (0.75–1.40)0.0457
 Pre-bronchodilator % predicted FEV139.90 (30.00–50.00)41.70 (31.10–51.60)38.00 (28.20–50.30)0.0015
 Post-bronchodilator FEV1, L1.24 (0.96–1.57)1.22 (0.94–1.55)1.17 (0.89–1.57)0.0603
 Post-bronchodilator % predicted FEV145.70 (35.45–56.00)46.50 (36.50–56.70)44.00 (32.60–54.95)0.0160
 Post-bronchodilator FEV1/FVC45.10 (36.80–53.90)46.80 (37.80–55.40)43.20 (35.35–52.50)0.0002
Reversibility at screening
 Reversibility, %13.00 (5.10–23.20)10.80 (3.20–19.40)12.70 (5.20–22.70)<0.0001
 Reversibility, mL140.00 (50.00–230.0)120.00 (30.00–200.0)130.00 (50.00–220.0)<0.0001
 Reversibility subgroup (≥12% and ≥200 mL increase)578 (33.0)224 (25.5)170 (29.2)0.0004
Lung function at baseline
 Post-bronchodilator FEV1, L1.17 (0.86–1.53)1.17 (0.88–1.49)1.10 (0.82–1.48)0.0222
 Post-bronchodilator % predicted FEV142.70 (32.00–53.95)44.10 (33.50–53.80)41.20 (29.85–52.65)0.0075
  • Data are n (%) or median (IQR) unless otherwise stated. Data presented include characteristics statistically significantly different (p<0.05) between clusters or imbalanced by treatment (p<0.05) within clusters (see online supplementary table S1).

  • BUN, blood urea nitrogen; COPD, chronic obstructive pulmonary disease; FEV1, forced expiratory volume in 1 s; FVC, forced vital capacity; WBC, white cell count.