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Table 1 Patient characteristics

From: Identification of chronic kidney disease patient characteristics influencing the renoprotective effects of febuxostat therapy: a retrospective follow-up study

 

All

sUA < 6.0 mg/dl

sUA ≥ 6.0 mg/dl

p value

Patients, n (%)

178

78

100

 

Male, n (%)

121 (68%)

42 (54%)

79 (79%)

< 0.001

Age, years (range)

65 (15–89)

66 (17–89)

64 (15–88)

n.s.

Baseline systolic BP, mmHg (range)

130 (85–180)

129 (85–170)

130 (96–180)

n.s.

Baseline diastolic BP, mmHg (range)

76 (45–110)

74 (50–110)

76 (45–106)

n.s.

Primary diseases of CKD

 Diabetic nephropathy, n (%)

33 (19%)

9 (12%)

24 (24%)

n.s.

 Chronic nephritis, n (%)

36 (20%)

19 (24%)

17 (17%)

n.s.

 Nephrosclerosis, n (%)

34 (19%)

14 (18%)

20 (20%)

n.s.

 Others, n (%)

75 (42%)

36 (46%)

39 (39%)

n.s.

Complications

 Diabetes mellitus, n (%)

45 (25%)

17 (22%)

28 (28%)

n.s.

 Hypertension, n (%)

137 (77%)

56 (72%)

81 (81%)

n.s.

 Abnormal cholesterol levels, n (%)

94 (53%)

34 (44%)

60 (60%)

n.s.

 Coronary artery disease, n (%)

12 (7%)

4 (5%)

8 (8%)

n.s.

Estimated GFR at baseline, ml/min/1.73 m2

27.0 (7.3–101.7)

27.7 (7.3–78.9)

26.0 (9–101.7)

n.s.

Urine protein levels at baseline, g/gCre

0.67 (0.00–17.7)

0.45 (0.00–7.2)

0.78 (0.00–17.7)

n.s.

Serum uric acid at baseline, mg/dl

8.3 (3.9–12.6)

8.3 (3.9–10.7)

8.7 (5.2–12.6)

0.042

CKD stage

 G1–2, n (%)

13 (7%)

6 (8%)

7 (7%)

n.s.

 G3, n (%)

62 (35%)

29 (37%)

33 (33%)

n.s.

 G4–5, n (%)

103 (58%)

43 (55%)

60 (60%)

n.s.

Antihyperuricemics before febuxostat

 None, n (%)

118 (66%)

58 (74%)

60 (60%)

n.s.

 Allopurinol, n (%)

44 (25%)

14 (18%)

30 (30%)

n.s

 Benzbromarone, n (%)

14 (8%)

6 (8%)

8 (8%)

n.s.

 Allopurinol and benzbromarone, n (%)

2 (1%)

0 (0%)

2 (2%)

n.s.

Febuxostat dose after 6 months

 10 mg/day, n (%)

103 (58%)

51 (66%)

52 (52%)

n.s.

 20 mg/day, n (%)

61 (34%)

22 (28%)

40 (39%)

n.s.

 40 mg/day, n (%)

14 (8%)

5 (6%)

9 (9%)

n.s.