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. 2015 Dec 24;33(4):511–514. doi: 10.1111/dme.13040

Table 1.

Baseline characteristics of patients with and without gastrointestinal side effects

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).

a

The homeostasis model assessment insulin resistance index was calculated using the formula: fasting insulin (pmol/l) × fasting glucose (mmol/l)/156.26.

b

Creatinine clearance was estimated using the Cockcroft–Gault formula.

c

Number of individuals concomitantly treated with OCT1 inhibiting drugs, including proton pump inhibitors, clopidogrel, doxazosin, verapamil, tramadol and citalopram 3, 5.

d

Data are presented as numbers of individuals (percentages).

e

Significance of test for comparison of combined genotype frequencies between the two groups under the additive model.