In recent years, the association between osteoporosis and atherosclerotic disease has
been described, regardless of patients' age, and highlighted epidemiologic and
pathophysiologic similarities between arterial wall calcification and
osteogenesis.[1,2]
Cross-sectional, prospective studies have pointed out significant negative association
between cardiovascular mortality and low bone mass, osteoporotic fractures, vascular
calcification, extension of coronary artery disease and abdominal aortic
injury.[3-5] Concomitant occurrence of both diseases
seems to result from common pathophysiologic and molecular mechanisms between these
conditions. However, it is still controversial whether a low bone mass is caused by
arterial calcification or vice-versa, or whether these conditions only have the same
pathophysiological mechanism.Risk factors for osteoporosis and atherosclerotic disease include estrogen, parathyroid
hormone, homocysteine and vitamin K deficiency, lipid oxidation products, inflammatory
process, vitamin D excess, molecular pathways involved in both bone and vascular
mineralization, and similar mechanisms of calcification involving vascular and bone
structures.[6] Arterial
calcification is found in more than 90% of atherosclerotic lesions. The process starts
with formation of vesicles in the endothelial matrix, followed by proliferation and
mineralization of the arterial intima-media wall, similarly to the bone tissue. Many
bone remodeling regulators have been described in calcified atherosclerotic lesions,
including osteocalcin, hydroxyapatite crystals, osteopontin, bone morphogenetic protein
2 osteoprotegerin, sclerostin, dickkopf factor (DKK), leptin, oxidized lipids and
calcium sensor-related factor.[7]Vascular atherosclerotic disease is more common in women with osteoporosis and osteopenia
as compared with women without these conditions.[5,6]
Increased mortality rates related to cardiovascular diseases have been reported at
advanced ages in postmenopausal women with low bone mineral density (BMD). Despite a
non-significant increase in myocardial infarction among women with low BMD, with a rate
of 22%, a significant increase is observed among men with low BMD, with a rate of
39%.[2]In the present issue, the study by Cheng et al.[8] adds to existing literature demonstrating an inverse association
between BMD and coronary artery disease in postmenopausal women. The authors studied 122
postmenopausal women with diagnosis of coronary artery diseases (acute coronary syndrome
or stable angina). All patients had undergone routine bone densitometry within one year
prior to the assessment of atherosclerotic load by the Gensini score and invasive
angiography. BMD of the femoral neck was measured by dual-energy X-ray absorptiometry.
The presence of osteopenia/osteoporosis in femoral neck was associated with increased
risk of severe coronary lesions. The multiple regression model revealed the T-scores as
independent predictors of higher Gensini scores. This study corroborates previous data
indicating an association between BMD and the severity of coronary atherosclerotic
disease, suggesting that this parameter may be an independent marker of disease
severity.Prospective studies including a larger number of patients and serial test data of BMD are
needed to establish the role of T-scores as risk predictors for the development of
severe coronary artery disease in men and women. Evidence from clinical practice
suggests that osteoporosispatients should also be assessed for the risk of severe
coronary artery disease.
Authors: Ludmila N Bakhireva; Elizabeth L Barrett-Connor; Gail A Laughlin; Donna Kritz-Silverstein Journal: Menopause Date: 2005-11-08 Impact factor: 2.953
Authors: Ihsane Hmamouchi; Fadoua Allali; Hamza Khazzani; Loubna Bennani; Leila El Mansouri; Linda Ichchou; Mohammed Cherkaoui; Redouane Abouqal; Najia Hajjaj-Hassouni Journal: BMC Public Health Date: 2009-10-14 Impact factor: 3.295
Authors: Viviane Cristina Uliana Peterle; Maria Rita Carvalho Garbi Novaes; Paulo Emiliano Bezerra Junior; João Carlos Geber Júnior; Rodrigo Tinôco Magalhães Cavalcante; Jurandi Barrozo da Silva Junior; Ray Costa Portela; Ana Patricia de Paula Journal: PLoS One Date: 2022-08-12 Impact factor: 3.752