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Table 3 Blood sampling test changes following empagliflozin exposure or placebo from baseline to 24 weeks

From: Effects of empagliflozin versus placebo on cardiac sympathetic activity in acute myocardial infarction patients with type 2 diabetes mellitus: the EMBODY trial

 

Empagliflozin (n = 46)

Placebo (n = 50)

Intergroup

Baseline

24 weeks

P

Baseline

24 weeks

P

P

HbA1c (%)

6.8 ± 1.0

6.6 ± 0.9

0.10

6.9 ± 0.9

6.8 ± 1.0

0.34

0.50

Hematocrit (%)

40.5 ± 4.6

44.2 ± 3.9

< 0.001

40.3 ± 4.2

40.5 ± 4.2

0.81

< 0.0001

Uric acid (mg/dL)

5.8 ± 1.4

4.9 ± 1.4

< 0.001

5.7 ± 1.5

5.8 ± 1.5

0.82

< 0.0001

eGFR (equivalent) (mL/min/1.73 m2)

64.6 ± 15.0

64.4 ± 16.8

0.84

66.1 ± 15.7

62.8 ± 15.4

0.02

0.10

Serum creatinine (mg/dL)

0.92 ± 0.19

0.94 ± 0.25

0.44

0.89 ± 0.20

0.94 ± 0.21

0.01

0.24

NT-pro BNP (pg/mL)

1028.7 ± 1105.6

370.3 ± 530.9

< 0.001

1270.6 ± 1521.0

673.7 ± 1151.1

< 0.001

0.91

Ketone bodies in the blood (venous blood) (μmol/L)

69.7 ± 51.8

119.3 ± 169.2

0.12

81.9 ± 70.9

61.2 ± 35.7

0.20

0.05

LDL-C (mg/dL)

87.5 ± 29.6

79.4 ± 21.3

0.06

87.8 ± 29.1

81.0 ± 25.0

0.09

0.83

HDL-C (mg/dL)

45.4 ± 12.7

49.8 ± 13.0

< 0.001

46.0 ± 10.2

49.2 ± 9.2

0.01

0.52

TG (mg/dL)

161.7 ± 119.7

145.5 ± 75.0

0.25

135.9 ± 54.3

141.0 ± 59.1

0.67

0.30

Non-HDL-C (mg/dL)

113.7 ± 40.5

102.3 ± 21.3

0.04

112.4 ± 32.2

105.2 ± 30.4

0.15

0.65

AST (U/L)

24.7 ± 7.9

23.2 ± 8.5

0.30

24.4 ± 10.3

25.4 ± 14.0

0.47

0.21

ALT (U/L)

26.4 ± 14.8

22.2 ± 13.1

0.04

26.6 ± 16.4

24.2 ± 11.9

0.20

0.54

γGTP (U/L)

39.6 ± 29.1

40.0 ± 40.2

0.92

32.4 ± 18.9

39.2 ± 38.1

0.03

0.16

  1. A1c, glycated hemoglobin; eGFR, estimated glomerular filtration rate; NT-Pro BNP: N-terminal pro b-type natriuretic peptide