(Sub) clinical cardiovascular disease is associated with increased bone loss and fracture risk; a systematic review of the association between cardiovascular disease and osteoporosis

被引:95
作者
den Uyl, Debby [2 ]
Nurmohamed, Mike T. [1 ,3 ]
van Tuyl, Lilian H. D. [2 ]
Raterman, Hennie G. [2 ]
Lems, Willem F. [2 ,3 ]
机构
[1] Vrije Univ Amsterdam Med Ctr, Dept Internal Med, NL-1081 NV Amsterdam, Netherlands
[2] Vrije Univ Amsterdam Med Ctr, Dept Rheumatol, NL-1081 NV Amsterdam, Netherlands
[3] Jan van Breemen Res Inst Reade, Dept Rheumatol, NL-1056 AB Amsterdam, Netherlands
关键词
CORONARY-HEART-DISEASE; VITAMIN-D-RECEPTOR; PERIPHERAL ARTERIAL-DISEASE; INTIMA-MEDIA THICKNESS; ATHEROSCLEROTIC VASCULAR-DISEASE; ABDOMINAL AORTIC CALCIFICATION; MUSCLE-CELL CALCIFICATION; MEXICAN-AMERICAN WOMEN; PULSE-WAVE VELOCITY; MATRIX GLA PROTEIN;
D O I
10.1186/ar3224
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Both cardiovascular disease and osteoporosis are important causes of morbidity and mortality in the elderly. The co-occurrence of cardiovascular disease and osteoporosis prompted us to review the evidence of an association between cardiovascular (CV) disease and osteoporosis and potential shared common pathophysiological mechanisms. Methods: A systematic literature search (Medline, Pubmed and Embase) was conducted to identify all clinical studies that investigated the association between cardiovascular disease and osteoporosis. Relevant studies were screened for quality according to guidelines as proposed by the Dutch Cochrane Centre and evidence was summarized. Results: Seventy studies were included in this review. Due to a large heterogeneity in study population, design and outcome measures a formal meta-analysis was not possible. Six of the highest ranked studies (mean n = 2,000) showed that individuals with prevalent subclinical CV disease had higher risk for increased bone loss and fractures during follow-up compared to persons without CV disease (range of reported risk: hazard ratio (HR) 1.5; odds ratio (OR) 2.3 to 3.0). The largest study (n = 31,936) reported a more than four times higher risk in women and more than six times higher risk in men. There is moderate evidence that individuals with low bone mass had higher CV mortality rates and incident CV events than subjects with normal bone mass (risk rates 1.2 to 1.4). Although the shared common pathophysiological mechanisms are not fully elucidated, the most important factors that might explain this association appear to be, besides age, estrogen deficiency and inflammation. Conclusions: The current evidence indicates that individuals with prevalent subclinical CV disease are at increased risk for bone loss and subsequent fractures. Presently no firm conclusions can be drawn as to what extent low bone mineral density might be associated with increased cardiovascular risk.
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页数:19
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