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Submitted on March 27, 2007
Accepted on October 22, 2007
Department of Obstetrics, Gynecology, and Reproductive Biology, Brigham and Women's Hospital, Boston, MA (J.R), Departments of Medicine (J.P.B., L.M.), Pharmacology (J.P.B.), and Radiology (S.J.S.) Columbia University College of Physicians and Surgeons, New York, New York
* To whom correspondence should be addressed. E-mail: ljm10{at}columbia.edu or lmr2@columbia.edu.
Background: Arterial calcification, a marker of atherosclerosis, results from a complex process of biomineralization resembling bone formation. Breast arterial calcification (BAC) has been associated with angiographic and clinical cardiovascular disease (CVD). The purpose of this study was to determine the association between reduced bone mineral density (BMD) and BAC, which may share a common pathophysiology.
Methods: We conducted a retrospective study of 228 women (55% Hispanic, mean age 64 ±10 yrs) who had both mammography and BMD evaluation at Columbia University Medical Center between 2001–2003. Each mammogram was reviewed for the presence of BAC using standardized methods. BMD was measured using dual-energy x-ray absorptiometry (DXA) and categorized as normal, low bone density (osteopenia) or osteoporosis as defined by the World Health Organization. Univariate and multivariate logistic regression analyses were performed to evaluate the association between reduced BMD and BAC.
Results: The prevalence of BAC, low bone density (osteopenia), and osteoporosis was 39%, 42%, and 29% respectively. Women with BAC were significantly more likely to be older, Hispanic, postmenopausal, and have osteoporosis as compared to women without BAC. In age-adjusted analyses, women with BAC were more likely to have reduced BMD (OR 3.0, P < 0.01) as compared to women without BAC. Furthermore, osteoporosis was strongly associated with the presence of BAC (OR 3.5, P < 0.01).
Conclusion: These data suggest that osteoporosis and arterial calcification are strongly and independently correlated. Reduced BMD may identify women at risk of vascular disease.
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