Skip to main content

Table 3 General patient characteristics

From: An analysis of DPV and DIVE registry patients with chronic kidney disease according to the finerenone phase III clinical trial selection criteria

 

Meta-analysis

DPV/DIVE patients with CKDa

 

FIDELITY

Total

Total ACEi/ARB

RCT ( +)

RCT (-)

p-value

 

n = 13,026

n = 65,168

n = 28,359

n = 12,322

n = 16,037

RCT + vs. -

Age, years, mean ± SD

64.8 ± 9.5

72.6 ± 12.1

73.4 ± 11.3

72.9 ± 10.6

73.7 ± 11.9

 < 0.0001

Gender, male, %

69.8

52.6

52.6

57.2

49.1

 < 0.0001

BMI, kg/m2, mean ± SD

31.3 ± 6.0

31.2 ± 6.9

31.5 ± 6.8

31.5 ± 6.7

31.5 ± 6.9

0.7183

Duration of diabetes, years, mean ± SD

15.4 ± 8.7

13.7 ± 10.0

13.9 ± 9.9

13.8 ± 9.9

14.0 ± 9.9

0.0423

Systolic blood pressure, mmHg, mean ± SD

136.7 ± 14.2

135.3 ± 18.7

136.6 ± 19.1

138.7 ± 19.2

135.0 ± 18.8

 < 0.0001

Diastolic blood pressure, mmHg, mean ± SD

76.4 ± 9.6

75.8 ± 10.8

76.0 ± 11.0

77.0 ± 11.0

75.3 ± 10.9

 < 0.0001

eGFR (CKD-EPI), mL/min/1.73 m2, mean ± SD

57.6 ± 21.7

54.2 ± 25.1

53.7 ± 24.0

60.1 ± 19.5

48.6 ± 26.0

 < 0.0001

  ≥ 60, %

39.9

31.3

30.8

49.8

15.8

 < 0.0001

 45 to < 60, %

26.4

29.1

29.6

23.4

34.5

 < 0.0001

 25 to < 45, %

32.5

29.1

29.9

26.9

32.3

 < 0.0001

  < 25, %

1.2

12.7

11.3

0.0

20.0

 < 0.0001

UACR, mg/g

      

  < 30, %

1.8

43.2

41.5

0.0

73.4

 < 0.0001

 30 to < 300, %

31.5

43.4

43.9

75.1

19.9

 < 0.0001

  ≥ 300, %

66.7

13.4

14.6

24.9

6.7

 < 0.0001

Serum potassium, mEq/L, mean ± SD

4.35 ± 0.44

4.39 ± 0.66b

4.41 ± 0.66c

4.4 ± 0.6

4.5 ± 0.7

 < 0.0001

HbA1c, %, mean (SD)

7.7 ± 1.4

7.6 ± 1.9

7.6 ± 1.9

7.7 ± 1.9

7.6 ± 1.8

 < 0.0001

  1. FIDELITY [21] was a pooled analysis of FIDELIO-DKD and FIGARO-DKD [19, 20]
  2. BMI body mass index; CKD-EPI Chronic Kidney Disease Epidemiology Collaboration; eGFR estimated glomerular filtration rate; IQR interquartile range; RCT randomized controlled trial; UACR urinary albumin-to-creatinine ratio
  3. aThe difference between the DPV/DIVE total and the combined RCT ± groups is the results of 36,809 patients that did not receive either ACEi or ARB at baseline
  4. bAvailable for 17,584 patients
  5. cAvailable for 10,022 patients