Macchi L, Christiaens L, Brabant S, Sorel N, Allal J, Mauco G, Brizard A
Laboratoire d'Hématologie et des Maladies du Sang, Hôpital La Miletrie, 86 000, Poitiers, France.
Thromb Res. 2002 Jul 15;107(1-2):45-9. doi: 10.1016/s0049-3848(02)00210-4.
Platelet activation plays an important role in arterial thrombosis and the widespread use of aspirin has reduced major events by 25% in the secondary prevention of cardiovascular diseases. However, it appears that aspirin antiplatelet effect is not uniform and 8-45% of the population are, in vitro, aspirin resistant, and it is well recognized that platelets can be activated by pathways that are not blocked by aspirin, such as adenosine diphosphate (ADP).
To investigate whether aspirin-resistant patients have a modified sensitivity to ADP-induced platelet activation
Seventy-two patients were enrolled. Platelet function was measured by the PFA-100(R) analyser; platelet GP IIb-IIIa activation by ADP 10 micro M was assessed by flow cytometry using PAC-1 MoAb.
Using a collagen/epinephrine coated cartridge on the PFA-100(R), the prevalence of aspirin resistance was 29.2% (n=21). For aspirin-resistant patients, the collagen/ADP coated cartridge showed a closure time significantly shorter (p=0.004) compared to the sensitive and control groups. Platelets from aspirin-resistant patients bound PAC-1 significantly more (p=0.03) than the aspirin-sensitive patients and controls when activated with 10 micro M ADP.
Platelets from aspirin-resistant patients appear to be more sensitive and activable by ADP. This hypersensitivity could provide a possible explanation for the so-called aspirin resistance, and this could justify therapeutic improvement with alternative antiplatelet agents.
血小板活化在动脉血栓形成中起重要作用,阿司匹林的广泛应用已使心血管疾病二级预防中的主要事件减少了25%。然而,阿司匹林的抗血小板作用似乎并不一致,8%至45%的人群在体外对阿司匹林耐药,并且人们普遍认识到血小板可通过阿司匹林未阻断的途径被激活,如二磷酸腺苷(ADP)。
研究阿司匹林抵抗患者对ADP诱导的血小板活化的敏感性是否改变。
纳入72例患者。使用PFA-100®分析仪测量血小板功能;使用PAC-1单克隆抗体通过流式细胞术评估10 μM ADP诱导的血小板糖蛋白IIb-IIIa活化。
在PFA-100®上使用胶原/肾上腺素包被的检测池,阿司匹林抵抗的发生率为29.2%(n = 21)。对于阿司匹林抵抗患者,与敏感组和对照组相比,胶原/ADP包被的检测池显示的封闭时间显著缩短(p = 0.004)。当用10 μM ADP激活时,阿司匹林抵抗患者的血小板与PAC-1的结合显著多于阿司匹林敏感患者和对照组(p = 0.03)。
阿司匹林抵抗患者的血小板似乎对ADP更敏感且更易被激活。这种超敏反应可能为所谓的阿司匹林抵抗提供一种解释,这可能为使用替代抗血小板药物进行治疗改进提供依据。