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Table 4 Comorbidity

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. -

Arterial hypertension, n (%)

96.5

78.0 (140/90)

100.0

100.0

100.0

1.0

Diabetic retinopathy, n (%)

38.0

6.0

7.5

7.5

7.5

0.9981

Diabetic neuropathy, n (%)

26.9

45.9

50.5

53.7

48.0

 < 0.0001

Lipid metabolism disorders, n (%)

45.6

87.4

91.6

92.0

91.2

0.0320

History of CV disease, n (%)

      

 Coronary artery disease w/o MI, n (%)

30.7

11.0

13.9

13.2

14.5

 < 0.0001

 Peripheral arterial disease, n (%)

16.0

23.8

27.2

27.5

27.0

0.3972

 Myocardial infarction, n (%)

15.5

10.2

13.0

12.3

13.5

0.0048

 Ischemic stroke, n (%)

11.9

9.0

11.7

11.6

11.7

0.8986

 Heart failure, n (%)

7.5

12.3

16.6

15.3

17.7

 < 0.0001

  1. FIDELITY [21] was a pooled analysis of FIDELIO-DKD and FIGARO-DKD [19, 20]
  2. CV cardiovascular; RCT randomized controlled trial
  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 an ACEi or ARB at baseline