Institut de Cardiologie, INSERM Unité Mixte de Recherche_S 937, Pitié-Salpêtrière Hospital, Paris, France.
JAMA. 2011 Oct 26;306(16):1765-74. doi: 10.1001/jama.2011.1529.
Despite dual antiplatelet therapy, stent thrombosis remains a devastating and unpredictable complication of percutaneous coronary intervention (PCI).
To perform a sequential analysis of clinical and genetic factors associated with definite early stent thrombosis.
DESIGN, SETTING, AND PARTICIPANTS: Case-control study conducted in 10 centers in France between January 2007 and May 2010 among 123 patients undergoing PCI who had definite early stent thrombosis and DNA samples available, matched on age and sex with 246 stent thrombosis-free controls.
Accuracy of early stent thrombosis prediction by 23 genetic variants.
Among the 23 genetic variants investigated in 15 different genes, the significant determinants of early stent thrombosis were CYP2C19 metabolic status (adjusted odds ratio [OR], 1.99; 95% CI, 1.47-2.69), ABCB1 3435 TT genotype (adjusted OR, 2.16; 95% CI, 1.21-3.88), and ITGB3 PLA2 carriage (adjusted OR, 0.52; 95% CI, 0.28-0.95). Nongenetic independent correlates were acuteness of PCI (adjusted OR, 3.05; 95% CI, 1.54-6.07), complex lesions (American College of Cardiology/American Heart Association type C) (adjusted OR, 2.33; 95% CI, 1.40-3.89), left ventricular function less than 40% (adjusted OR, 2.25; 95% CI, 1.09-4.70), diabetes mellitus (adjusted OR, 1.82; 95% CI, 1.02-3.24), use of proton pump inhibitors (adjusted OR, 2.19; 95% CI, 1.29-3.75), and higher clopidogrel loading doses (adjusted OR, 0.73; 95% CI, 0.57-0.93). The discriminative accuracy of the clinical-only model was similar to that of a genetic-only model (area under the curve, 0.73 [95% CI, 0.67-0.78] vs 0.68 [95% CI, 0.62-0.74], respectively; P = .34). A combined clinical and genetic model led to a statistically significant increase in the discriminatory power of the model compared with the clinical-only model (area under the curve, 0.78 [95% CI, 0.73-0.83] vs 0.73 [95% CI, 0.67-0.78]; P = .004).
This case-control study identified 3 genes (CYP2C19, ABCB1, and ITGB3) and 2 clopidogrel-related factors (loading dose and proton pump inhibitors) that were independently associated with early stent thrombosis. Future studies are needed to validate the prognostic accuracy of these risk factors in prospective cohorts.
尽管进行了双联抗血小板治疗,支架血栓仍然是经皮冠状动脉介入治疗(PCI)的一种具有破坏性且难以预测的并发症。
对与明确的早期支架血栓形成相关的临床和遗传因素进行连续分析。
设计、设置和参与者:在法国 10 个中心进行的病例对照研究,于 2007 年 1 月至 2010 年 5 月期间在 123 例接受 PCI 并发生明确的早期支架血栓形成且有 DNA 样本的患者中进行,这些患者与 246 例无支架血栓形成的对照组按年龄和性别匹配。
23 种遗传变异对早期支架血栓形成的预测准确性。
在所研究的 15 个不同基因中的 23 种遗传变异中,早期支架血栓形成的显著决定因素为 CYP2C19 代谢状态(调整后的比值比[OR],1.99;95%CI,1.47-2.69)、ABCB1 3435 TT 基因型(调整后的 OR,2.16;95%CI,1.21-3.88)和 ITGB3 PLA2 携带(调整后的 OR,0.52;95%CI,0.28-0.95)。非遗传独立相关因素为 PCI 的紧迫性(调整后的 OR,3.05;95%CI,1.54-6.07)、复杂病变(美国心脏病学会/美国心脏协会 C 型)(调整后的 OR,2.33;95%CI,1.40-3.89)、左心室功能低于 40%(调整后的 OR,2.25;95%CI,1.09-4.70)、糖尿病(调整后的 OR,1.82;95%CI,1.02-3.24)、质子泵抑制剂的使用(调整后的 OR,2.19;95%CI,1.29-3.75)和更高的氯吡格雷负荷剂量(调整后的 OR,0.73;95%CI,0.57-0.93)。仅临床模型的判别准确性与仅遗传模型相似(曲线下面积,0.73[95%CI,0.67-0.78]与 0.68[95%CI,0.62-0.74],分别为 P =.34)。与仅临床模型相比,联合临床和遗传模型显著提高了模型的判别能力(曲线下面积,0.78[95%CI,0.73-0.83]与 0.73[95%CI,0.67-0.78];P =.004)。
这项病例对照研究确定了 3 个基因(CYP2C19、ABCB1 和 ITGB3)和 2 个与氯吡格雷相关的因素(负荷剂量和质子泵抑制剂)与早期支架血栓形成独立相关。需要进一步的前瞻性队列研究来验证这些危险因素的预后准确性。