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. 2021 Apr 17;13(4):1344. doi: 10.3390/nu13041344

Table 1.

Baseline characteristics of the study population receiving dietary supplementation of selenium and coenzyme Q10 combined or placebo during four years.

Active Treatment Group
n = 106
Placebo Group
n = 107
p-Value
Age years, mean (SD) 77.0 (3.7) 77.0 (3.3) 0.36
Gender, Males/Females 43/64 46/61
History
Diabetes, n (%) 25 (23.6) 21 (19.6) 0.51
Smoking, n (%) 9 (8.5) 12 (11.2) 0.50
Hypertension, n (%) 75 (70.8) 75 (70.1) 0.92
IHD, n (%) 18 (17.0) 22 (20.6) 0.50
NYHA class I, n (%) 54 (50.9) 57 (53.3) 0.73
NYHA class II, n (%) 33 (31.1) 26 (24.3) 0.27
NYHA class III, n (%) 19 (17.9) 23 (21.5) 0.51
NYHA class IV, n (%) 0 0
Medications
ACEI/ARB, n (%) 18 (17.0) 20 (18.7) 0.74
Beta blockers, n (%) 32 (30.2) 24 (22.4) 0.20
Diuretics, n (%) 29 (27.4) 32 (29.9) 0.68
Statins, n (%) 20 (18.9) 20 (18.7) 0.97
Examinations
EF < 40%, n (%) 2 (1.9) 7 (6.5) 0.20
s-selenium pre-intervention µg/L, mean (SD) 67.6 (14.8) 66.3 (15.8) 0.98

Note: ACEI: ACE- inhibitors; ARB: Angiotension receptor blockers; EF: Ejection fraction; IHD: Ischemic heart disease; NYHA: New York Heart Association functional class; SD: Standard Deviation. Note: Values are means ± SDs or frequency (percent). Note: Student’s unpaired two-sided t-test was used for continuous variables and the chi-square test was used for analysis of one discrete variable.