Vascular function and skeletal fragility: a study of tonometry, brachial hemodynamics, and bone microarchitecture

被引:2
作者
Usiskin, Ilana M. [1 ]
Mitchell, Gary F. [2 ]
Bouxsein, Mary L. [3 ]
Liu, Ching-Ti [4 ]
Kiel, Douglas P. [5 ,6 ,7 ]
Samelson, Elizabeth J. [5 ,6 ,7 ]
机构
[1] Brigham & Womens Hosp, Div Rheumatol Inflammat & Immun, 75 Francis Str, Boston, MA 02115 USA
[2] Cardiovasc Engn Inc, Norwood, MA 02062 USA
[3] Beth Israel Deaconess Med Ctr, Ctr Adv Orthoped Studies CAOS, Dept Orthoped Surg, Boston, MA 02215 USA
[4] Boston Univ, Sch Publ Hlth, Dept Biostat, Boston, MA 02118 USA
[5] Hebrew Sr Life, Hinda & Arthur Marcus Inst Aging Res, Boston, MA 02131 USA
[6] Beth Israel Deaconess Med Ctr, Dept Med, Boston, MA 02215 USA
[7] Harvard Med Sch, Boston, MA 02115 USA
关键词
bone; microarchitecture; finite element analysis; HR-pQCT; osteoporosis; aging; vascular function; epidemiology; FLOW-MEDIATED DILATION; ABDOMINAL AORTIC CALCIFICATION; MINERAL DENSITY; ARTERIAL STIFFNESS; CARDIOVASCULAR-DISEASE; RISK-FACTORS; OSTEOPOROSIS; ASSOCIATION; PRESSURE; FRACTURE;
D O I
10.1093/jbmr/zjae071
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Osteoporosis and cardiovascular disease frequently occur together in older adults; however, a causal relationship between these 2 common conditions has not been established. By the time clinical cardiovascular disease develops, it is often too late to test whether vascular dysfunction developed before or after the onset of osteoporosis. Therefore, we assessed the association of vascular function, measured by tonometry and brachial hemodynamic testing, with bone density, microarchitecture, and strength, measured by HR-pQCT, in 1391 individuals in the Framingham Heart Study. We hypothesized that decreased vascular function (pulse wave velocity, primary pressure wave, brachial pulse pressure, baseline flow amplitude, and brachial flow velocity) contributes to deficits in bone density, microarchitecture and strength, particularly in cortical bone, which is less protected from excessive blood flow pulsatility than the trabecular compartment. We found that individuals with increased carotid-femoral pulse wave velocity had lower cortical volumetric bone mineral density (tibia: -0.21 [-0.26, -0.15] standardized beta [95% CI], radius: -0.20 [-0.26, -0.15]), lower cortical thickness (tibia: -0.09 [-0.15, -0.04], radius: -0.07 [-0.12, -0.01]) and increased cortical porosity (tibia: 0.20 [0.15, 0.25], radius: 0.21 [0.15, 0.27]). However, these associations did not persist after adjustment for age, sex, height, and weight. These results suggest that vascular dysfunction with aging may not be an etiologic mechanism that contributes to the co-occurrence of osteoporosis and cardiovascular disease in older adults. Further study employing longitudinal measures of HR-pQCT parameters is needed to fully elucidate the link between vascular function and bone health. Osteoporosis and heart disease are both medical conditions that commonly develop in older age. It is not known whether abnormal functioning of blood vessels contributes to the development of bone fragility with aging. In this study, we investigated the relationship between impaired blood vessel function and bone density and micro-structure in a group of 1391 people enrolled in the Framingham Heart Study. Blood vessel function was measured using specialized tools to assess blood flow and pressure. Bone density and micro-structure were measured using advanced imaging called HR-pQCT. We found that people with impaired blood vessel function tended to have lower bone density and worse deterioration in bone micro-structure. However, once we statistically controlled for age and sex and other confounders, we did not find any association between blood vessel function and bone measures. Overall, our results showed that older adults with impaired blood vessel function do not exhibit greater deterioration in the skeleton.
引用
收藏
页码:906 / 917
页数:12
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