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. 2020 Jun 30;2020:7262474. doi: 10.1155/2020/7262474

Table 1.

Baseline characteristics of the study population according to the treatment arms.

Resveratrol
(n = 30)
Placebo
(n = 30)
Age (year) 65.8 ± 1.9 67.5 ± 2.1
Male 22 (73%) 21 (70%)
Ejection fraction (%) 30.06 ± 1.04 31.70 ± 1.27
NT-proBNP (pg/ml) 2998 ± 507 3139 ± 446
Serum creatinine (μmol/l) 99.77 ± 4.42 104.47 ± 4.82
Sys. BP (mmHg) 132.47 ± 3.4 128.77 ± 3.8
Dias. BP (mmHg) 79.1 ± 2.33 80.13 ± 2.66
Heart rate (beat/min) 72.2 ± 2.75 76.93 ± 2.5
Etiological factors
Ischemic heart disease 17 (56.7%) 17 (56.7%)
Nonischemic (alcohol, chemotherapy, and myocarditis) 13 (43.3%) 13 (43.3%)
Risk factors, comorbidities
Hypertension 22 (73%) 23 (76%)
Diabetes 13 (43%) 14 (46%)
Smoking 11 (36%) 8 (27%)
Pulmonary diseases (asthma, COPD) 7 (23%) 8 (27%)
BMI (kg/m2) 29.3 ± 0.9 30.4 ± 1.3
Target heart rate (>70/min) 23 (76.7%) 20 (66.7%)
Atrial fibrillation 7 (23%) 10 (33.3%)
Concomitant treatment
ACE inhibitor/ARB 28 (93%) 29 (97%)
Beta-blocker 29 (97%) 28 (93%)
MRA 23 (76.7%) 21 (70%)
Ivabradine 6 (20%) 6 (20%)
Diuretics
Loop diuretics (furosemide, etacrynic acid) 27 (90%) 28 (93%)
Thiazide or thiazide-like diuretics (hypothiazide, indapamide, etc.) 8 (27%) 9 (30%)
Device therapy
CRT-P/D 9 (30%) 7 (23.2%)
ICD 4 (13%) 3 (10%)

Baseline characteristics of the study population according to the treatment arms. Values are expressed as mean ± SEM. There were no significant differences in characteristics between RES- (resveratrol-) and placebo-treated groups at baseline. ACEI: angiotensin-converting enzyme inhibitors; ARB: angiotensin receptor blocker; BMI: body mass index; COPD: chronic obstructive pulmonary disease; CRT-P/D: cardiac resynchronization therapy-pacemaker/defibrillator; Dias. BP: diastolic blood pressure; ICD: implantable cardioverter-defibrillator; MRA: mineralocorticoid receptor antagonist; NT-proBNP: N-terminal prohormone of brain natriuretic peptide; Sys. BP: systolic blood pressure.