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. 2016 Jun 8;2016:1064924. doi: 10.1155/2016/1064924

Table 5.

The results of the two groups on the further efficacy and safety variables.

Treatment group Control group p value
(n = 47) (n = 44)
SBP (mmHg) 119.00 (115.00, 127.00) 119.00 (109.25, 127.00) 0.415
DBP (mmHg) 78.00 (75.00, 80.00) 76.00 (72.00, 80.00) 0.111
HbA1c (%) 7.67 ± 0.24 7.50 ± 0.20 0.066
AST (μ/L) 20.00 (16.00, 25.00) 18.50 (16.00, 23.75) 0.650
ALT (μ/L) 18.0 (14.00, 26.00) 19.50 (15.25, 24.50) 0.827
BUN (mmol/L) 5.19 ± 0.18 5.13 ± 0.24 0.832
Scr (μmol/L) 63.00 (56.00, 75.00) 62.00 (54.25, 80.75) 0.921
HDL (mmol/L) 1.23 (1.11, 1.46) 1.20 (0.99, 1.65) 0.586
LDL (mmol/L) 2.58 ± 0.10 2.77 ± 0.16 0.296
TG (mmol/L) 1.22 (0.87, 1.56) 1.14 (0.53, 1.80) 0.984
TC (mmol/L) 4.44 ± 0.13 4.67 ± 0.17 0.136

Data are expressed as the mean ± SD for normal distribution. Nonnormally distributed values are presented as median (interquartile range). p values represent the treatment group versus the control group. represent p < 0.05 versus baseline (week 0), paired t-test for normal distribution or Wilcoxon matched-pairs signed-rank test for nonnormal distribution. SBP, systolic blood pressure; DBP, diastolic blood pressure; AST, aspartate transaminase. ALT, alanine transaminase; BUN, blood urea nitrogen; Scr, serum creatinine; HDL, high density lipoprotein cholesterol; LDL, low density lipoprotein cholesterol; TG, triglycerides; TC, total cholesterol.