van der Toorn Janine E, Vernooij Meike W, Ikram M Arfan, Kavousi Maryam, Bos Daniel
Department of Epidemiology, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Department of Radiology and Nuclear Medicine, Erasmus MC, University Medical Center, Rotterdam, The Netherlands.
Eur Radiol. 2024 Aug;34(8):5142-5152. doi: 10.1007/s00330-023-10566-7. Epub 2024 Jan 15.
There is a lack of information on the development of arteriosclerosis over time. This study aims to assess long-term sex-specific changes in arterial calcifications in five arteries, and the influence of cardiovascular risk factors hereon.
From a population-based cohort, 807 participants (mean baseline age, 65.8; SD, 4.2) underwent a non-contrast computed tomography (CT) examination between 2003 and 2006, and after a median follow-up of 14 years. We assessed incidences and changes in volumes of coronary artery calcification (CAC), aortic arch calcification (AAC), extracranial (ECAC) and intracranial carotid artery calcification (ICAC), and vertebrobasilar artery calcification (VBAC). We investigated the simultaneous presence of severe progression (upper quartile of percentual change volumes). Associations of cardiovascular risk factors with changes in calcification volumes were assessed using multivariate linear regression models.
The difference in AAC was most substantial; the median volume (mm) increased from of 129 to 916 in men and from 93 to 839 in women. For VBAC, no change in volumes was observed though more than a quarter of participants without baseline VBAC developed VBAC during follow-up. Severe progression was most often observed in only one artery at the same time. Hypertension was most consistently associated with increase in calcifications. Associations of diabetes, hypercholesterolemia, and smoking with changes in calcifications varied across arteries and sex.
We found a considerable incidence and increase in volumes of calcifications in different arteries, over a 14-year time interval. Cardiovascular risk factors were associated with increase of calcifications with sex-specific differential effects across arteries.
There is a considerable incidence and increase in volumes of calcifications in different arteries, over a 14-year time interval. Cardiovascular risk factors are associated with increase of calcifications with sex-specific differential effects across arteries; thus, assessing changes in only one artery may thus not provide a good reflection of the systemic development of arteriosclerosis.
• Assessing change in arterial calcification in only one artery does not reflect the systemic development of arterial calcification. • Cardiovascular risk factors are associated with progression of arterial calcifications. • Progression of arterial calcification is sex and artery-specific.
目前缺乏关于动脉硬化随时间发展的信息。本研究旨在评估五条动脉中动脉钙化的长期性别特异性变化,以及心血管危险因素对此的影响。
从一个基于人群的队列中,807名参与者(平均基线年龄65.8岁;标准差4.2)在2003年至2006年间接受了非增强计算机断层扫描(CT)检查,并进行了中位随访14年。我们评估了冠状动脉钙化(CAC)、主动脉弓钙化(AAC)、颅外(ECAC)和颅内颈动脉钙化(ICAC)以及椎基底动脉钙化(VBAC)的发生率和体积变化。我们调查了严重进展(百分比变化体积的上四分位数)的同时存在情况。使用多元线性回归模型评估心血管危险因素与钙化体积变化的关联。
AAC的差异最为显著;男性的中位体积(mm)从129增加到916,女性从93增加到839。对于VBAC,虽然超过四分之一无基线VBAC的参与者在随访期间出现了VBAC,但体积未观察到变化。严重进展最常仅在一条动脉中同时观察到。高血压与钙化增加最一致相关。糖尿病、高胆固醇血症和吸烟与钙化变化的关联因动脉和性别而异。
我们发现在14年的时间间隔内,不同动脉中钙化的发生率和体积有相当大的增加。心血管危险因素与钙化增加相关,且在不同动脉中有性别特异性差异效应。
在14年的时间间隔内,不同动脉中钙化的发生率和体积有相当大的增加。心血管危险因素与钙化增加相关,且在不同动脉中有性别特异性差异效应;因此,仅评估一条动脉的变化可能无法很好地反映动脉硬化的全身发展情况。
• 仅评估一条动脉的钙化变化不能反映动脉钙化的全身发展情况。• 心血管危险因素与动脉钙化进展相关。• 动脉钙化进展具有性别和动脉特异性。