Mutschlechner David, Tscharre Maximilian, Wadowski Patricia P, Pultar Joseph, Weikert Constantin, Lee Silvia, Eichelberger Beate, Panzer Simon, Perkmann Thomas, Gremmel Thomas
Department of Internal Medicine I, Cardiology and Intensive Care Medicine, Landesklinikum Mistelbach-Gänserndorf, 2130 Mistelbach, Austria.
Department of Internal Medicine, Cardiology and Nephrology, Landesklinikum Wiener Neustadt, 2700 Wiener Neustadt, Austria.
J Clin Med. 2023 Feb 17;12(4):1627. doi: 10.3390/jcm12041627.
Bleeding events in patients with acute coronary syndrome (ACS) are a risk factor for adverse outcomes, including mortality. We investigated the association of growth differentiation factor (GDF)-15, an established predictor of bleeding complications, with on-treatment platelet reactivity in ACS patients undergoing coronary stenting receiving prasugrel or ticagrelor. Platelet aggregation was measured by multiple electrode aggregometry (MEA) in response to adenosine diphosphate (ADP), arachidonic acid (AA), thrombin receptor-activating peptide (TRAP, a protease-activated receptor-1 (PAR-1) agonist), AYPGKF (a PAR-4 agonist) and collagen (COL). GDF-15 levels were measured using a commercially available assay. GDF-15 correlated inversely with MEA ADP (r = -0.202, = 0.004), MEA AA (r = -0.139, = 0.048) and MEA TRAP (r = -0.190, = 0.007). After adjustment, GDF-15 was significantly associated with MEA TRAP ( = -0.150, = 0.044), whereas no significant associations were detectable for the other agonists. Patients with low platelet reactivity in response to ADP had significantly higher GDF-15 levels ( = 0.005). In conclusion, GDF-15 is inversely associated with TRAP-inducible platelet aggregation in ACS patients treated with state-of-the-art antiplatelet therapy and significantly elevated in patients with low platelet reactivity in response to ADP.
急性冠状动脉综合征(ACS)患者的出血事件是包括死亡率在内的不良结局的危险因素。我们研究了已被证实的出血并发症预测因子生长分化因子(GDF)-15与接受普拉格雷或替格瑞洛治疗的冠状动脉支架置入ACS患者治疗期间血小板反应性之间的关联。通过多电极聚集测定法(MEA)测量血小板对二磷酸腺苷(ADP)、花生四烯酸(AA)、凝血酶受体激活肽(TRAP,一种蛋白酶激活受体-1(PAR-1)激动剂)、AYPGKF(一种PAR-4激动剂)和胶原(COL)的聚集情况。使用市售检测方法测量GDF-15水平。GDF-15与MEA ADP(r = -0.202,P = 0.004)、MEA AA(r = -0.139,P = 0.048)和MEA TRAP(r = -0.190,P = 0.007)呈负相关。调整后,GDF-15与MEA TRAP显著相关(β = -0.150,P = 0.044),而其他激动剂未发现显著关联。对ADP反应性低的血小板患者GDF-15水平显著更高(P = 0.005)。总之,在接受最先进抗血小板治疗的ACS患者中,GDF-15与TRAP诱导的血小板聚集呈负相关,且对ADP反应性低的患者中GDF-15显著升高。