Table 1.
Group without gastrointestinal side effects (n = 49) | Group with gastrointestinal side effects (n = 43) | P | |
---|---|---|---|
Age (years) | 58.8 ± 8.4 | 57.1 ± 9.5 | 0.365 |
Women/men (% women) | 22/27 (44.9) | 32/11 (74.4) | 0.004 |
Weight (kg) | 93.7 ± 15.8 | 85.2 ± 13.8 | 0.007 |
BMI (kg/m2) | 31.7 ± 4.2 | 30.4 ± 4.3 | 0.128 |
Fasting plasma glucose (mmol/l) | 8.0 (7.5–9.2) | 8.2 (7.5–9.2) | 0.573 |
Fasting plasma insulin (pmol/l) | 95.0 (57.0–154.0) | 120.5 (70.0–186.0) | 0.246 |
HOMA‐IRa | 4.4 (2.9–8.1) | 6.1 (3.7–8.9) | 0.198 |
HbA1c (mmol/l) | 56 (51–63) | 58 (53–66) | 0.376 |
HbA1c (%) | 7.3 (6.8–7.9) | 7.5 (7.0–8.2) | |
Total cholesterol (mmol/l) | 5.2 ± 1.3 | 5.3 ± 1.2 | 0.690 |
HDL‐cholesterol (mmol/l) | 1.02 ± 0.23 | 1.18 ± 0.25 | 0.002 |
LDL‐cholesterol (mmol/l) | 3.27 ± 1.27 | 3.10 ± 1.09 | 0.523 |
Triglycerides (mmol/l) | 1.93 (1.53–3.13) | 2.22 (1.40–3.18) | 0.997 |
Creatinine (μmol/l) | 84.1 ± 17.8 | 71.9 ± 16.2 | 0.001 |
Creatinine clearance (ml/min)b | 109.1 ± 28.9 | 109.0 ± 31.8 | 0.983 |
Metformin daily dose (mg) | 1000 (821–1500) | 1000 (960–1700) | 0.492 |
Use of OCT1 inhibiting drugsc | 6 (14.0%) | 8 (16.3%) | 0.752 |
Number of OCT1 reduced‐function alleles (0/1/2)d | 30/17/2 (61.2%/34.7%/4.1%) | 18/20/5 (41.9%/46.5%/11.6%) | 0.048e |
Data are presented as means ± sd, medians (interquartile range) or numbers (percentages).
The homeostasis model assessment insulin resistance index was calculated using the formula: fasting insulin (pmol/l) × fasting glucose (mmol/l)/156.26.
Creatinine clearance was estimated using the Cockcroft–Gault formula.
Number of individuals concomitantly treated with OCT1 inhibiting drugs, including proton pump inhibitors, clopidogrel, doxazosin, verapamil, tramadol and citalopram 3, 5.
Data are presented as numbers of individuals (percentages).
Significance of test for comparison of combined genotype frequencies between the two groups under the additive model.