From the Department of Biomedical Engineering, School of Engineering and School of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama.
Division of Cardiovascular Disease, Heersink School of Medicine, The University of Alabama at Birmingham, Birmingham, Alabama.
ASAIO J. 2023 Jun 1;69(6):569-575. doi: 10.1097/MAT.0000000000001886. Epub 2023 Mar 31.
Nonsurgical bleeding occurs in a significant proportion of patients implanted with continuous-flow ventricular assist devices (CF-VADs) and is associated with nonphysiologic flow with diminished pulsatility. An in vitro vascular pulse perfusion model seeded with adult human aortic endothelial cells (HAECs) was used to identify biomarkers sensitive to changes in pulsatility. Diminished pulsatility resulted in an ~45% decrease in von Willebrand factor (vWF) levels from 9.80 to 5.32 ng/ml (n = 5, p < 0.05) and a threefold increase in angiopoietin-2 (ANGPT-2) levels from 775.29 to 2471.93 pg/ml (n = 5, p < 0.05) in cultured HAECs. These changes are in agreement with evaluation of patient blood samples obtained pre-CF-VAD implant and 30-day postimplant: a decrease in plasma vWF level by 50% from ~45.59 to ~22.49 μg/ml (n = 15, p < 0.01) and a 64% increase in plasma ANGPT-2 level from 7,073 to 11,615 pg/ml (n = 8, p < 0.05). This study identified vWF and ANGPT-2 as highly sensitive to changes in pulsatility, in addition to interleukin-6 (IL-6), IL-8, and tumor necrosis-α (TNF-α). These biomarkers may help determine the optimal level of pulsatility and help identify patients at high risk of nonsurgical bleeding.
非手术性出血在植入持续流动心室辅助装置 (CF-VAD) 的患者中占很大比例,与非生理性流动和搏动减弱有关。本研究使用体外血管脉冲灌注模型,该模型中接种了成人主动脉内皮细胞 (HAEC),以鉴定对搏动变化敏感的生物标志物。搏动减弱导致血管性血友病因子 (vWF) 水平从 9.80ng/ml 降至 5.32ng/ml(n=5,p<0.05),下降约 45%,而血管生成素-2 (ANGPT-2) 水平从 775.29pg/ml 增至 2471.93pg/ml(n=5,p<0.05),增加三倍。这些变化与植入 CF-VAD 前和植入后 30 天患者血液样本的评估一致:血浆 vWF 水平降低 50%,从45.59μg/ml 降至22.49μg/ml(n=15,p<0.01),而血浆 ANGPT-2 水平增加 64%,从 7073pg/ml 增至 11615pg/ml(n=8,p<0.05)。本研究发现 vWF 和 ANGPT-2 对搏动变化非常敏感,除白细胞介素-6 (IL-6)、白细胞介素-8 (IL-8) 和肿瘤坏死-α (TNF-α) 外。这些生物标志物可能有助于确定最佳搏动水平,并帮助识别非手术性出血风险较高的患者。