Department of Vascular Surgery (G04129), University Medical Centre Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.
Department of Cardiology, Amsterdam University Medical Centres, Amsterdam, The Netherlands.
Sci Rep. 2021 Sep 23;11(1):18946. doi: 10.1038/s41598-021-98177-4.
Plasma osteoprotegerin (OPG) and vascular smooth muscle cell (VSMC) derived extracellular vesicles (EVs) are important regulators in the process of vascular calcification (VC). In population studies, high levels of OPG are associated with events. In animal studies, however, high OPG levels result in reduction of VC. VSMC-derived EVs are assumed to be responsible for OPG transport and VC but this role has not been studied. For this, we investigated the association between OPG in plasma and circulating EVs with coronary artery calcium (CAC) as surrogate for VC in symptomatic patients. We retrospectively assessed 742 patients undergoing myocardial perfusion imaging (MPI). CAC scores were determined on the MPI-CT images using a previously developed automated algorithm. Levels of OPG were quantified in plasma and two EV-subpopulations (LDL and TEX), using an electrochemiluminescence immunoassay. Circulating levels of OPG were independently associated with CAC scores in plasma; OR 1.39 (95% CI 1.17-1.65), and both EV populations; EV-LDL; OR 1.51 (95% CI 1.27-1.80) and EV-TEX; OR 1.21 (95% CI 1.02-1.42). High levels of OPG in plasma were independently associated with CAC scores in this symptomatic patient cohort. High levels of EV-derived OPG showed the same positive association with CAC scores, suggesting that EV-derived OPG mirrors the same pathophysiological process as plasma OPG.
血浆骨保护素(OPG)和血管平滑肌细胞(VSMC)衍生的细胞外囊泡(EVs)是血管钙化(VC)过程中的重要调节剂。在人群研究中,高水平的 OPG 与事件有关。然而,在动物研究中,高水平的 OPG 导致 VC 减少。VSMC 衍生的 EVs 被认为负责 OPG 的运输和 VC,但这一作用尚未得到研究。为此,我们研究了在有症状的患者中,血浆中 OPG 与冠状动脉钙(CAC)作为 VC 替代物的循环 EVs 之间的相关性。我们回顾性评估了 742 例行心肌灌注成像(MPI)的患者。使用先前开发的自动算法,在 MPI-CT 图像上确定 CAC 评分。使用电化学发光免疫分析法定量检测血浆和两种 EV 亚群(LDL 和 TEX)中的 OPG 水平。循环 OPG 水平与血浆中 CAC 评分独立相关;OR1.39(95%CI1.17-1.65),以及两种 EV 群体;EV-LDL;OR1.51(95%CI1.27-1.80)和 EV-TEX;OR1.21(95%CI1.02-1.42)。在该症状患者队列中,血浆中高水平的 OPG 与 CAC 评分独立相关。高水平的 EV 衍生 OPG 与 CAC 评分呈相同的正相关,表明 EV 衍生 OPG 反映了与血浆 OPG 相同的病理生理过程。