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Table 2 Major clinical parameters during the trial

From: Baseline urate level and renal function predict outcomes of urate-lowering therapy using low doses of febuxostat and benzbromarone: a prospective, randomized controlled study in a Chinese primary gout cohort

 

Baseline

4 weeks

8 weeks

12 weeks

sUA, μmol/L

 Febuxostat

561.10 ± 71.63

405.43 ± 78.20##

429.41 ± 94.71##

404.27 ± 81.10##

 Benzbromarone

554.90 ± 66.73

381.58 ± 92.8##

400.57 ± 79.91##

390.91 ± 92.87##

CCr, mL/min

 Febuxostat

105.93 ± 30.61

108.17 ± 32.14

108.61 ± 30.73

110.87 ± 30.93##,*

 Benzbromarone

108.86 ± 29.12

108.25 ± 27.27

108.15 ± 28.41

108.08 ± 28.78

Cr, μmol/L

 Febuxostat

84.21 ± 15.10

82.39 ± 14.65#

83.38 ± 14.55

80.83 ± 15.13##,*

 Benzbromarone

81.13 ± 12.19

81.63 ± 12.03

79.83 ± 9.82

82.14 ± 12.48

BUN, mmol/L

 Febuxostat

5.56 ± 1.21*

5.66 ± 1.19

5.69 ± 1.39

5.59 ± 1.45

 Benzbromarone

5.02 ± 1.40

4.84 ± 1.33

5.00 ± 1.36

5.83 ± 7.90

TG, mmol/L

 Febuxostat

1.70 ± 0.65

1.98 ± 0.85#,**

2.03 ± 1.15#,*

1.97 ± 0.89*

 Benzbromarone

1.93 ± 0.93

1.81 ± 0.89

1.95 ± 1.04

1.87 ± 0.85

TC, mmol/L

 Febuxostat

4.95 ± 0.93

4.94 ± 0.95

4.89 ± 0.88

5.02 ± 0.87

 Benzbromarone

5.21 ± 0.98

5.12 ± 0.91

5.27 ± 0.92

5.20 ± 0.88

ALT, U/L

 Febuxostat

32.45 ± 15.96

43.77 ± 22.10##,**

42.73 ± 24.13##,**

42.88 ± 24.20##,*

 Benzbromarone

27.74 ± 13.87

29.96 ± 19.74

28.05 ± 15.18

30.08 ± 20.94

AST, U/L

 Febuxostat

22.90 ± 11.38

26.97 ± 11.22##,*

25.365 ± 7.88##

27.32 ± 14.59##,**

 Benzbromarone

22.16 ± 6.87

22.88 ± 9.76

22.21 ± 7.63

22.75 ± 8.64

GLU, mmol/L

 Febuxostat

5.76 ± 0.57

5.63 ± 0.60

5.73 ± 0.66

5.74 ± 0.75

 Benzbromarone

5.76 ± 0.93

5.67 ± 1.03

5.65 ± 0.59

5.80 ± 0.94

  1. Data given as mean ± SEM. *P ≤ 0.05, **P ≤ 0.01, Feb group vs. Ben group. #P ≤ 0.05, ##P ≤ 0.01, before vs. after treatment