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. 2022 Apr 29;14(9):1879. doi: 10.3390/nu14091879

Table 1.

Baseline characteristics of the participants.

Placebo/SAx
(n = 33)
SAx/Placebo
(n = 34)
Gender (Female %, n) 78.79 (26) 79.41 (27)
Age (years) 53.21 ± 4.2 52.79 ± 4.8
Smoking (Smokers %, n) 18.18 (6) 26.47 (9)
Weight (kg) 66.26 ± 11.8 64.08 ± 10.9
BMI (kg/m2) 24.64 ± 2.9 24.56 ± 3.2
Waist circumference (cm) 80.51 ± 9.2 82.58 ± 9.8
FM (%) 29.18 ± 6.7 28.76 ± 6.4
FFM (%) 70.82 ± 6.7 71.24 ± 6.4
MM (%) 48.03 ± 7.7 47.87 ± 5.5
SBP (mmHg) 110.3 ± 13.1 110.9 ± 12.9
DBP (mmHg) 74.06 ± 10.8 73.75 ± 9.5
HR (bpm) 67.36 ± 8.9 70.41 ± 7.5
TC (mg/dL) 226.7 ± 29.6 224.6 ± 35.4
LDL-C (mg/dL) 144.3 ± 23.9 145.3 ± 28.6
HDL-C (mg/dL) 66.25 ± 12.9 62.00 ± 12.6
TG (mg/dL) 80.56 ± 24.6 86.52 ± 44.0

Data presented as means ± standard deviations (SDs). SAx: oral supplementation with hydroxytyrosol (HT) and punicalagin (PC); BMI: body mass index; FM: fat mass; FFM: fat-free mass; MM: muscle mass; SBP: systolic blood pressure; DBP: diastolic blood pressure; HR: heart rate; TC: total cholesterol; LDL-C: low-density lipoprotein cholesterol; HDL-C: high-density lipoprotein cholesterol; and TG: triglycerides. There were no significant differences in the baseline state between the two intervention sequences.