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Table 1 Patients’ characteristics and comparison between patients with bronchial hyperresponsiveness who responded (CVA patients) and not responded (non-CVA patients) to anti-asthmatic therapy

From: Does bronchial hyperresponsiveness predict a diagnosis of cough variant asthma in adults with chronic cough: a cohort study

 

All patients (N = 49)

Non-CVA (6; 12.2%)

CVA (43; 87.8%)

P value

Age (years)

60.0 (54.0–68.0)

54.5 (45.0–56.0)

61.0 (55.0–69.0)

0.0961

Gender (N female, %)

40 (81.6%)

5 (83.3%)

35 (81.4%)

0.6540

Cough duration (months)

48.0 (24.0–120.0)

84.0 (36.0–204.0)

48.0 (24.0–120.0)

0.5190

Smoking status (N ex-smokers, %)

12 (24.5%)

0 (0%)

31 (27.9%)

0.3260

Blood eosinophil count (cells/μL)

197.4 (128.3–303.7)

235.3 (157.5–405.0)

189.0 (120.7–284.2)

0.2578

BMI (kg/m2)

30.2 (25.8–33.1)

28.6 (26.8–31.4)

30.2 (24.7–33.2)

0.9878

FEV1 (% predicted)

86.0 (80.0–100.0)

92.5 (85.0–101.0)

86.0 (80.0–100.0)

0.4453

FeNO (ppb)

17.5 (12.2–27.0)

13.5 (10.9–24.5)

17.9 (13.7–27.1)

0.2891

PC20 (mg/mL)

2.0 (0.8–4.4)

2.2 (0.7–3.2)

2.0 (0.8–5.0)

0.6583

PC20 < 1 mg/mL (N patients, %)

14 (28.6%)

2 (33.3%)

12 (27.9%)

0.5590

PC20 < 4 mg/mL (N patients, %)

35 (71.4%)

5 (83.3%)

30 (69.8%)

0.4410

Sputum neutrophil percentage (%)

43.0 (34.0–52.0)

62.0 (49.0–62.0)

41.5 (31.5–51.5)

0.0291

Sputum eosinophil percentage (%)

1.0 (0.0–4.0)

0.0 (0.0–3.0)

1.0 (0.0–4.0)

0.5999

Atopy (N patients, %)

23 (46.7%)

2 (33.3%)

21 (48.8%)

0.7820

UACS (N patients, %)

38 (77.6%)

5 (83.3%)

33 (76.7%)

0.8730

GER (N patients, %)

27 (55.1%)

6 (100%)

21 (48.8%)

0.0183

Initial LCQ (points)

10.4 (8.4–13.1)

9.9 (9.1–10.9)

10.7 (8.3–13.8)

0.6148

Change in LCQ due to treatment (points)

4.8 (2.2–6.2)

1.8 (0.2–3.6)

4.9 (3.1–6.5)

0.0153

Initial VAS (mm)

69.0 (43.5–80.0)

57.5 (40.0–80.0)

69.0 (49.0–80.0)

0.4729

Change in VAS due to treatment (mm)

38.0 (27.0–56.0)

8.0 (− 15.0 to 35.0)

41.0 (27.0–58.0)

0.0188

Initial capsaicin threshold C2 (μmol/L)

5.9 (2.0–15.7)

1.5 (1.0–6.4)

7.8 (3.4–15.7)

0.0338

Initial capsaicin threshold C5 (μmol/L)

7.8 (3.9–15.7)

5.9 (2.4–19.5)

7.8 (3.9–15.7)

0.4994

Final capsaicin threshold C2 (μmol/L)

3.9 (2.0–15.7)

1.0 (0.5–1.0)

5.9 (3.9–15.7)

0.0073

Final capsaicin threshold C5 (μmol/L)

7.8 (3.9–15.7)

1.0 (1.0–3.9)

11.7 (3.9–15.7)

0.0219

Change in the capsaicin threshold C2 after treatment (μmol/L)a

0 (− 1.5 to 3.9)

− 0.5 (− 6.9 to 0)

0 (0–3.9)

0.1248

Change in the capsaicin threshold C5 after treatment (μmol/L)a

0 (0–7.8)

− 6.8 (− 30.2 to 0)

0 (0–11.8)

0.0466

  1. Data are presented as median and interquartile range or numbers and percentages. Statistical analysis included Mann–Whitney U or χ2 test
  2. CVA cough variant asthma, BMI body mass index, PC20 provocative concentration of methacholine causing 20% fall in FEV1, FeNO fractional exhaled nitric oxide, UACS upper airway cough syndrome, GER gastroesophageal reflux, C2 the lowest capsaicin concentrations of capsaicin evoking two coughs, C5 the lowest capsaicin concentrations of capsaicin evoking five coughs, LCQ Leicester Cough Questionnaire, VAS visual analogue scale
  3. aDifference between final and baseline C2/C5 threshold