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骨密度与主动脉瓣和二尖瓣环钙化的长期进展:动脉粥样硬化的多民族研究。

Bone mineral density and long-term progression of aortic valve and mitral annular calcification: The Multi-Ethnic Study of Atherosclerosis.

机构信息

Leon H. Charney Division of Cardiology, NYU Grossman School of Medicine, New York, NY, USA.

Department of Biostatistics, University of Washington, Seattle, WA, USA.

出版信息

Atherosclerosis. 2021 Oct;335:126-134. doi: 10.1016/j.atherosclerosis.2021.08.031. Epub 2021 Aug 26.

Abstract

BACKGROUND AND AIMS

Bone and mineral metabolism has been implicated in the pathophysiology of cardiac valve calcification. Whether bone demineralization, a common aging-related disorder, promotes calcific valve disease remains uncertain. We tested the hypothesis that low bone mineral density (BMD) is associated with greater incidence/progression of cardiac valve calcification in the Multi-Ethnic Study of Atherosclerosis.

METHODS

Using linear mixed-effects models, we related baseline measurement of BMD of the thoracic vertebrae by computed tomography (CT) in 6768 participants to serial CT assessments of aortic valve calcification (AVC) and mitral annular calcification (MAC) obtained over a >10-year period.

RESULTS

After multivariable adjustment, lower BMD (per SD decrement) was associated with accelerated increase in AVC over time in women (0.76 [95% CI 0.42,1.09] Agatston -units [AU]/year) and men (1.41 [95% CI 0.48,2.33] AU/year), as well as for MAC in women (3.22 [95% CI 1.16,5.28] AU/year) and men (3.59 [95% CI 2.09,5.09] AU/year). Significant effect modification was observed, with more pronounced BMD-related acceleration of AVC and MAC progression in older or white participants of one or both sexes, as well as by estimated glomerular filtration rate, though the latter differed by sex for AVC and MAC.

CONCLUSIONS

In this multi-ethnic cohort, low thoracic BMD was significantly, but modestly, associated with increased AVC and MAC progression. This suggests that altered bone mineral metabolism does not have a major impact on calcific valve disease in the general population, but the possibility of a more meaningful influence in higher-risk individuals with osteoporosis will require further investigation.

摘要

背景与目的

骨骼和矿物质代谢与心脏瓣膜钙化的病理生理学有关。去矿化,一种常见的与年龄相关的疾病,是否会促进钙化性瓣膜病尚不确定。我们检验了这样一个假设,即低骨密度(BMD)与动脉瓣钙化(AVC)和二尖瓣环钙化(MAC)的发生率/进展程度呈正相关。

方法

我们使用线性混合效应模型,将 6768 名参与者的胸腰椎 CT 基线 BMD 测量值与超过 10 年期间获得的主动脉瓣钙化(AVC)和二尖瓣环钙化(MAC)的连续 CT 评估相关联。

结果

经多变量调整后,与女性(0.76[95%CI 0.42,1.09]Agatston 单位[AU]/年)和男性(1.41[95%CI 0.48,2.33]AU/年)的 AVC 随时间的加速增加相比,BMD 较低(每 SD 降低)与 AVC 和 MAC 的增加相关,女性(3.22[95%CI 1.16,5.28]AU/年)和男性(3.59[95%CI 2.09,5.09]AU/年)。观察到明显的效应修饰,在两性中年龄较大或为白人的参与者,或两性中估计肾小球滤过率较高的参与者,BMD 与 AVC 和 MAC 进展的相关性更强。然而,AVC 和 MAC 的性别差异与估计肾小球滤过率不同。

结论

在这个多民族队列中,较低的胸腰椎 BMD 与 AVC 和 MAC 进展显著相关,但相关性适中。这表明,改变的矿物质代谢对普通人群的钙化性瓣膜病没有重大影响,但在骨质疏松症高危人群中,其对钙化性瓣膜病的影响可能更有意义,需要进一步研究。

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