Experimental Metabolism and Clinical Research Laboratory, Clinical Research Department, Division of Biomedical Research, Centro Médico Nacional "20 de Noviembre", Instituto de Seguridad y Servicios Sociales para los Trabajadores del Estado, Mexico City P.O. 03100, Mexico.
Vascular Surgery and Angiology Department, Centro Médico Nacional "20 de Noviembre", Instituto de Seguridad y Servicios Sociales para los Trabajadores del Estado, Mexico City P.O. 03100, Mexico.
Cells. 2023 Feb 11;12(4):584. doi: 10.3390/cells12040584.
Critical limb ischemia represents an advanced stage of peripheral arterial disease. Angioplasty improves blood flow to the limb; however, some patients progress irreversibly to lower limb amputation. Few studies have explored the predictive potential of biomarkers during postangioplasty outcomes.
To evaluate the behavior of endothelial progenitor cells in patients with critical limb ischemia, in relation to their postangioplasty outcome.
Twenty patients with critical limb ischemia, candidates for angioplasty, were enrolled. Flow-mediated dilation, as well as endothelial progenitor cells (subpopulations CD45+/CD34+/CD133+/CD184+ and CD45+/CD/34+/KDR[VEGFR-2]+ estimated by flow cytometry) from blood flow close to vascular damage, were evaluated before and after angioplasty. Association with lower limb amputation during a 30-day follow-up was analyzed.
Endothelial progenitor cells were related with flow-mediated dilation. A higher number of baseline EPCs CD45CD34KDR, as well as an impaired reactivity of endothelial progenitor cells CD45CD34CD133CD184 after angioplasty, were observed in cases further undergoing major limb amputation, with a significant discrimination ability and risk (0.75, specificity 0.83 and RR 4.5 < 0.05).
Endothelial progenitor cells were related with endothelial dysfunction, whereas a higher baseline number of the subpopulation CD45CD34KDR, as well as an impaired reactivity of subpopulation CD45CD34CD133CD184 after angioplasty, showed a predictive ability for major limb amputation in patients with critical limb ischemia.
严重肢体缺血代表外周动脉疾病的晚期阶段。血管成形术可改善肢体血流,但部分患者会不可逆转地进展为下肢截肢。很少有研究探讨生物标志物在血管成形术后结果中的预测潜力。
评估严重肢体缺血患者血管成形术后内皮祖细胞的行为与血管成形术后结果的关系。
纳入 20 名严重肢体缺血、拟行血管成形术的患者。在血管成形术前和术后,通过血流介导的扩张以及通过流式细胞术估计的内皮祖细胞(亚群 CD45+/CD34+/CD133+/CD184+和 CD45+/CD/34+/KDR[VEGFR-2]+)评估血流接近血管损伤处的内皮祖细胞。分析与 30 天随访期间下肢截肢的关系。
内皮祖细胞与血流介导的扩张有关。在进一步接受主要肢体截肢的病例中,基线时 EPCs CD45CD34KDR 的数量较高,以及血管成形术后内皮祖细胞 CD45CD34CD133CD184 的反应受损,观察到具有显著的区分能力和风险(0.75,特异性 0.83 和 RR 4.5 < 0.05)。
内皮祖细胞与内皮功能障碍有关,而基线时 CD45CD34KDR 亚群数量较高,以及血管成形术后 CD45CD34CD133CD184 亚群反应受损,可预测严重肢体缺血患者的主要肢体截肢。