Radiation Chemistry and Biospectroscopy, Chemical Engineering School, National Technical University of Athens, Athens, Greece;
Radiation Chemistry and Biospectroscopy, Chemical Engineering School, National Technical University of Athens, Athens, Greece.
In Vivo. 2022 Jan-Feb;36(1):189-197. doi: 10.21873/invivo.12690.
BACKGROUND/AIM: The pathogenesis, treatment and prevention of atherosclerosis continue to be the subject of intensive research and study by the scientific community. Based on Fourier-transform infrared spectra and 3D-Doppler echogram, we attempted to develop a computational simulation model for predicting the association of atherosclerotic risk factors with pathogenic molecular structural changes.
Atheromatic carotid arteries from 56 patients (60-85 years old) were used as samples. Color 3D-Doppler echogram screening was performed on all patients preoperatively. Each infrared spectrum consisted of 120 co-added spectra at a spectral resolution of 4 cm Results: The infrared spectral analysis reveals 'marker bands', such as the 1,744 cm band assigned to aldehyde formation and to the 'fingerprint' digital spectral region of 1,050-1,169 cm, characteristic of the presence of advanced glycation end products (C-O-C). The accumulation of calcium phosphate salts increases the formation rate of stenosis. The critical point of stenosis risk starts at about 45%, while when stenosis is over 60-70%, the risk of ischemic stroke or other major adverse cardiovascular events increases dramatically.
Fourier-transform infrared spectroscopy and mathematical simulation models showed that carotid artery stenosis over 45% reduces the blood flow rate, while stenosis over 65% dramatically increases the hemodynamic disturbance, with a parallel increase the rate of ischemic stroke or other major adverse cardiovascular events.
背景/目的:动脉粥样硬化的发病机制、治疗和预防仍然是科学界研究的热点。基于傅里叶变换红外光谱和 3D 多谱勒超声图,我们试图开发一种计算模拟模型,以预测动脉粥样硬化危险因素与致病分子结构变化的相关性。
从 56 例患者(60-85 岁)的粥样硬化颈动脉中获取样本。所有患者术前均进行彩色 3D 多谱勒超声图筛查。每个红外光谱由 120 个光谱叠加而成,光谱分辨率为 4cm。
红外光谱分析显示出“标记带”,如 1744cm 处的醛形成带和 1050-1169cm 处的“指纹”数字光谱区域,特征为晚期糖基化终产物(C-O-C)的存在。钙磷酸盐盐的积累增加了狭窄形成的速度。狭窄风险的临界点约为 45%,而当狭窄超过 60-70%时,缺血性中风或其他主要不良心血管事件的风险急剧增加。
傅里叶变换红外光谱和数学模拟模型表明,颈动脉狭窄超过 45%会降低血流速度,而狭窄超过 65%会显著增加血液动力学紊乱,同时缺血性中风或其他主要不良心血管事件的发生率也会增加。