Table 1

Baseline characteristics of patients

Amlodipine group (n=49)Control group (n=49)p Value
Age in years (mean±SD)69±1069±120.87
Male sex, n (%)31 (%)26 (%)0.31
Risk factors/history, n (%)
 Smoking2 (4%)3 (4%)0.64
 Diabetes mellitus22 (44%)27 (55%)0.23
 Hypertension48 (98%)46 (94%)0.31
 Previous myocardial infarction*21 (43%)26 (53%)0.31
 ACS within 1 month†22 (45%)15 (30%)0.15
Concomitant medications, n (%)
 Pantoprazole30 (61%)27 (55%)0.53
 ACE inhibitor33 (67%)34 (69%)0.83
 Angiotensin receptor blocker10 (20%)8 (16%)0.60
 β-blocker34 (69%)35 (71%)0.82
 Spironolactone4 (8%)4 (8%)1.00
 α-blocker2 (4%)6 (12%)0.14
 Digoxin0 (0%)3 (6%)0.08
 Heparin‡5 (10%)8 (16%)0.37
 Cytochrome P450 3A4 metabolising statin§45 (92%)44 (90%)0.72
 Serotonin-selective inhibitor0 (0%)0 (0%)1.00
 Amiodarone0 (0%)0 (0%)1.00
 Ginkgo biloba (herb)0 (0%)0 (0%)1.00
Laboratory data (mean±SD)
 Hb, g/dl13±1.813±2.00.31
 Platelets, 109/l213±55208±540.69
 Creatinine, μmol/l100±2998±290.74
 Bilirubin, μmol/l9±3.711±6.00.18
Baseline platelet reactivity at day 0 (mean±SD)
 P2Y12 reactivity unit206±82213±910.72
 Platelet inhibition, %38±2337±210.78
  • *Any history of myocardial infarction, defined as elevated troponin with either ischaemic chest pain or ECG change.

  • †Acute coronary syndrome defined as Unstable angina, non-ST elevation or ST-elevation myocardial infarction within 1 month before enrolment.

  • ‡Heparin used between 7 and 2 days before enrolment.

  • §Only simvastatin or atorvastatin used.