Filatova Anastasiia Yu, Afanasieva Olga I, Arefieva Tatiana I, Potekhina Alexandra V, Tyurina Alexandra V, Klesareva Elena A, Razova Oksana A, Ezhov Marat V, Pokrovsky Sergey N
Institute of Experimental Cardiology, National Medical Research Center of Cardiology Named after Academician E.I. Chazov, Ministry of Health of the Russian Federation, 121552 Moscow, Russia.
A.L. Myasnikov Institute of Clinical Cardiology, National Medical Research Center of Cardiology Named after Academician E.I. Chazov, Ministry of Health of the Russian Federation, 121552 Moscow, Russia.
J Pers Med. 2023 Jun 29;13(7):1077. doi: 10.3390/jpm13071077.
In this study we analyzed the concentration of lipoprotein(a) (Lp(a)), PCSK9-Lp(a) complexes and the circulating monocyte subsets in coronary atherosclerosis. For this study, 257 patients with coronary atherosclerosis and 68 patients without stenotic atherosclerosis in the coronary, carotid and lower extremity arteries (control group) were enrolled. The monocyte subpopulations (classical CD14++CD16-, intermediate CD14++CD16+ and non-classical CD14+CD16++) were analyzed by direct immunofluorescence and flow cytometry. The Lp(a) and PCSK9-Lp(a) complexes in the serum were detected by ELISA. The concentration of Lp(a) was higher in the coronary atherosclerosis group compared with the controls (23.0 (9.1; 73.3) mg/dL versus 10.7 (4.7; 25.0) mg/dL, < 0.05). No correlations between the level of Lp(a) and the concentration of the PCSK9-Lp(a) complexes, nor between the level of Lp(a) or PCSK9 and the total number of monocytes, were observed in either group. A slight positive correlation between the concentration of PCSK9-Lp(a) complexes and the absolute level of monocytes was obtained (r = 0.20, = 0.002) in the patients with atherosclerosis due to the intermediate monocyte subsets (r = 0.33, = 0.04). According to regression analysis, both the PCSK9-Lp(a) complexes concentration and BMI were related to the absolute number of blood monocytes in patients with atherosclerosis. Further studies are required to determine the pathogenetic contribution of PCSK9-Lp(a) complexes to the development of atherosclerosis.
在本研究中,我们分析了冠状动脉粥样硬化患者中脂蛋白(a)(Lp(a))、PCSK9-Lp(a)复合物的浓度以及循环单核细胞亚群。本研究纳入了257例冠状动脉粥样硬化患者和68例冠状动脉、颈动脉和下肢动脉无狭窄性动脉粥样硬化的患者(对照组)。通过直接免疫荧光和流式细胞术分析单核细胞亚群(经典型CD14++CD16-、中间型CD14++CD16+和非经典型CD14+CD16++)。采用酶联免疫吸附测定法检测血清中的Lp(a)和PCSK9-Lp(a)复合物。冠状动脉粥样硬化组的Lp(a)浓度高于对照组(23.0(9.1;73.3)mg/dL对10.7(4.7;25.0)mg/dL,<0.05)。两组中均未观察到Lp(a)水平与PCSK9-Lp(a)复合物浓度之间、Lp(a)或PCSK9水平与单核细胞总数之间存在相关性。在动脉粥样硬化患者中,由于中间单核细胞亚群,PCSK9-Lp(a)复合物浓度与单核细胞绝对水平之间存在轻微正相关(r = 0.20, = 0.002)(r = 0.33, = 0.04)。根据回归分析,PCSK9-Lp(a)复合物浓度和体重指数均与动脉粥样硬化患者血液单核细胞的绝对数量有关。需要进一步研究以确定PCSK9-Lp(a)复合物对动脉粥样硬化发展的致病作用。