Table 1. Risk factors for MI in three case–control studies.
Study 1 | Study 2 | Study 3 | ||||
Cases (n = 762) | Controls (n = 857) | Cases (n = 579) | Controls (n = 1159) | Cases (n = 475) | Controls (n = 619) | |
Male, % | 60 | 41 | 81 | 42 | 61 | 62 |
Age at enrollment, median (range) | 62 (29–87) | 65 (24–100) | 66(28–88) | 58 (45–97) | 60 (32–86) | 58 (37–88) |
Age at MI, median (range) | 52 (27–82) | NA | 57 (21–70) | NA | 53 (29–77) † | NA |
Smoking, % | 66 | 45 | 68 | 40 | 73 | 54 |
Diabetes, % | 20 | 0‡ | 25 | 0‡ | 38 | 10 |
Dyslipidemia§, % | 84 | 53 | 84 | 61 | 95 | 56 |
Hypertension||, % | 61 | 32 | 66 | 33 | 96 | 78 |
BMI (kg/m2), mean±SD | 28±5 | 26±5 | 28±5 | 26±5 | 31±6 | 30±7 |
Data available for 254 cases.
Individuals with diabetes were excluded from control group.
Dyslipidemia was defined in Study 1 and Study 2 to be self-reported history of a physician diagnosis of dyslipidemia or the use of lipid lowering prescription medication(s) and defined in Study 3 to be the use of lipid lowering prescription medication(s), LDL cholesterol >129 mg/dL, triglycerides >149 mg/dL or HDL cholesterol <45 mg/dL .
Hypertension was defined in Study 1 and Study 2 to be a self–reported history of a physician diagnosis of hypertension or use of antihypertensive prescription medication(s) and defined in Study 3 to be the use of antihypertensive prescription medication(s), systolic blood pressure >160 mmHg, or diastolic blood pressure >90 mmHg.
NA; not applicable.