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. 2016 Jan 14;2:91–96. doi: 10.1016/j.conctc.2015.12.008

Table 1.

Characteristics of participants at recruitment.

Simvastatin group Placebo group
N 9 9
Age, years 69.3 ± 7.2 66.4 ± 4.6
Male, n (%) 8 (88.9) 7 (77.8)
BMI, kg/m2 30.0 ± 4.7 28.5 ± 6.5
Smoking exposure, pack-years 50.0 ± 33.5 50.4 ± 14.0
GOLD A, n (%) 4 (44.4) 3 (33.3)
GOLD B, n (%) 1 (11.1) 1 (11.1)
GOLD C, n (%) 3 (33.3) 3 (33.3)
GOLD D, n (%) 1 (11.1) 2 (22.2)
Total cholesterol, mg/dL 183.6 ± 29.2 197.6 ± 27.9
Glycemia, mg/dL 106.3 ± 17.9 107.6 ± 18.7
Hemoglobin, g/dL 14.9 ± 1.1 14.2 ± 1.6
Comorbidities
Arterial hypertension, n (%)
Diabetes mellitus, n (%)
6 (66.7)
2 (22.2)
6 (66.7)
2 (22.2)
LA-β2, n (%) 8 (88.9) 7 (77.8)
LA Anticholinergic, n (%) 7 (77.8) 6 (66.7)
Inhaled corticosteroids, n (%) 6 (66.7) 7 (77.8)
SA-β2, n (%) 4 (44.4) 2 (22.2)
SA Anticholinergic, n (%) 1 (11.1) 2 (22.2)
ASA, n (%)
ACEI, n (%)
ARBs, n (%)
Diuretics, n (%)
2 (22.2)
2 (22.2)
2 (22.2)
2 (22.2)
2 (22.2)
3 (33.3)
2 (22.2)
2 (22.2)

N: number of patients; BMI: body mass index, LA: Long-acting, SA: short-acting, ASA: acetylsalicylic acid, ACEI: angiotensin converting enzyme inhibitor; ARBs angiotensin II receptor blocker.