Table 2. Odds ratios (OR) and 95% confidence intervals (95% CI) of first myocardial infarction (MI) after breast cancer diagnosis associated with subject characteristics and medical history.
Characteristics | # of cases/# of controls | Univariate OR (95% CI) | Multivariatea OR (95% CI) |
---|---|---|---|
Race/ethnicity | |||
Black | 19/45 | 0.8 (0.5–1.5) | 0.6 (0.3–1.1) |
White | 97/191 | 1.0 (referent) | 1.0 (referent) |
Other/unknown | 18/26 | 1.4 (0.7–2.6) | 1.2 (0.6–2.5) |
Body mass index at MI (kg/m2) b | |||
<25 | 52/105 | 1.0 (referent) | 1.0 (referent) |
25–29.9 | 38/79 | 0.9 (0.6–1.6) | 0.8 (0.4–1.4) |
>30 | 31/58 | 1.1 (0.6–1.9) | 0.8 (0.4–1.5) |
Unknown | 13/20 | ||
Oral contraceptive use ever | |||
No | 93/201 | 1.0 (referent) | 1.0 (referent) |
Yes | 25/43 | 1.5 (0.8–3.0) | 1.5 (0.7–3.0) |
Unknown | 16/18 | ||
Use of oestrogen and/or hormone replacement therapy ever | |||
No | 60/105 | 1.0 (referent) | 1.0 (referent) |
Yes | 69/147 | 0.8 (0.5–1.2) | 0.9 (0.5–1.4) |
Unknown | 5/10 | ||
Smoking status at MI b | |||
Never | 70/156 | 1.0 (referent) | 1.0 (referent) |
Ever | 59/100 | 1.3 (0.8–2.0) | 1.5 (0.9–2.4) |
Unknown | 5/6 | ||
History of hypertension | |||
No | 34/111 | 1.0 (referent) | 1.0 (referent) |
Yes, no medication | 7/28 | 0.8 (0.3–2.1) | 0.7 (0.3–2.0) |
Yes, medication | 93/123 | 2.5 (1.5–4.0) | 2.1 (1.3–3.4) |
History of diabetes | |||
No | 88/217 | 1.0 (referent) | 1.0 (referent) |
Yes, no medication | 8/13 | 1.5 (0.6–4.2) | 1.5 (0.6–4.2) |
Yes, medication | 38/32 | 3.2 (1.8–5.6) | 3.0 (1.6–5.6) |
History of hypercholesterolemia | |||
No | 68/150 | 1.0 (referent) | 1.0 (referent) |
Yes, no medication | 34/76 | 1.0 (0.6–1.8) | 1.1 (0.6–2.0) |
Yes, medication | 32/36 | 2.0 (1.1–3.7) | 1.4 (0.7–2.7) |
Multivariate model includes categorical items for the named characteristic, histories of hypertension and diabetes, smoking and a combined item for tamoxifen and radiation treatment.
As control subjects had no MI, data are from the reference date that marks the end of control subjects' at-risk period, which began at control subjects' dates of breast cancer diagnosis and extended for the duration of the matched case patients' time from breast cancer to MI diagnoses.