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Table 3 Between-group differences in changes at week 24 for clinical measures of interest in subgroups stratified by baseline serum insulin concentration

From: Association between serum insulin levels and heart failure-related parameters in patients with type 2 diabetes and heart failure treated with canagliflozin: a post-hoc analysis of the randomized CANDLE trial

Parameter

Treatment effect measures

Baseline serum insulin concentration < 7.5 mU/L

Baseline serum insulin concentration ≥ 7.5 mU/L

p-value for interaction

SBP, mmHg

Difference (canagliflozin minus glimepiride) in change

3.082 (− 2.423 to 8.587)

− 1.621 (− 7.026 to 3.784)

0.232

BMI, kg/m2

− 0.933 (− 1.474 to − 0.393)

− 1.590 (− 2.130 to − 1.050)

0.092

ePV, %

− 6.500 (− 12.933 to − 0.066)

− 7.477 (− 13.847 to − 1.106)

0.832

eGFR, mL/min/1.73m2

0.679 (− 2.552 to 3.910)

− 1.736 (− 4.938 to 1.465)

0.298

HbA1c, %

0.229 (− 0.055 to 0.513)

0.498 (0.214 to 0.782)

0.189

Uric acid, mg/dL

− 1.057 (− 1.485 to − 0.655)

− 0.859 (− 1.266 to − 0.452)

0.498

Triglycerides, mg/dL

0.372 (− 29.247 to 29.990)

4.462 (− 25.061 to 33.985)

0.848

HDL-C, mg/dL

4.559 (1.366 to 7.752)

1.812 (− 1.352 to 4.976)

0.231

LDL-C, mg/dL

0.924 (− 7.180 to 9.029)

5.555 (− 2.498 to 13.608)

0.427

NT-proBNP*

Ratio (canagliflozin vs. glimepiride) of proportional change

0.946 (0.752 to 1.190)

0.977 (0.782 to 1.222)

0.840

  1. *Log-transformed. Data are shown as mean (95% confidence interval)
  2. Abbreviations, see Tables 1 and 2