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PEAR1基因变异与血小板聚集及心血管疾病转归相关。

Genetic variation in PEAR1 is associated with platelet aggregation and cardiovascular outcomes.

作者信息

Lewis Joshua P, Ryan Kathleen, O'Connell Jeffrey R, Horenstein Richard B, Damcott Coleen M, Gibson Quince, Pollin Toni I, Mitchell Braxton D, Beitelshees Amber L, Pakzy Ruth, Tanner Keith, Parsa Afshin, Tantry Udaya S, Bliden Kevin P, Post Wendy S, Faraday Nauder, Herzog William, Gong Yan, Pepine Carl J, Johnson Julie A, Gurbel Paul A, Shuldiner Alan R

机构信息

Division of Endocrinology, Diabetes, and Nutrition, University of Maryland School of Medicine, Baltimore, MD 21201, USA.

出版信息

Circ Cardiovasc Genet. 2013 Apr;6(2):184-92. doi: 10.1161/CIRCGENETICS.111.964627. Epub 2013 Feb 7.

Abstract

BACKGROUND- Aspirin or dual antiplatelet therapy with aspirin and clopidogrel is a standard therapy for patients who are at increased risk for cardiovascular events. However, the genetic determinants of variable response to aspirin (alone and in combination with clopidogrel) are not known. METHODS AND RESULTS- We measured ex vivo platelet aggregation before and after dual antiplatelet therapy in individuals (n=565) from the Pharmacogenomics of Anti-Platelet Intervention (PAPI) Study and conducted a genome-wide association study of drug response. Significant findings were extended by examining genotype and cardiovascular outcomes in 2 independent aspirin-treated cohorts: 227 percutaneous coronary intervention patients and 1000 patients of the International Verapamil SR/Trandolapril Study (INVEST) Genetic Substudy (INVEST-GENES). Results from the genome-wide association study revealed a strong association between single-nucleotide polymorphisms on chromosome 1q23 and post-dual antiplatelet therapyplatelet aggregation. Further genotyping revealed rs12041331 in the platelet endothelial aggregation receptor-1 (PEAR1) gene to be most strongly associated with dual antiplatelet therapy response (P=7.66×10(-9)). In white and black patients undergoing percutaneous coronary intervention, A-allele carriers of rs12041331 were more likely to experience a cardiovascular event or death compared with GG homozygotes (hazard ratio, 2.62; 95% confidence interval, 0.96-7.10; P=0.059; and hazard ratio, 3.97; 95% confidence interval, 1.10-14.31; P=0.035, respectively). In aspirin-treated INVEST-GENES patients, rs12041331 A-allele carriers had significantly increased risk of myocardial infarction compared with GG homozygotes (odds ratio, 2.03; 95% confidence interval, 1.01-4.09; P=0.048). CONCLUSION- Common genetic variation in PEAR1 may be a determinant of platelet response and cardiovascular events in patients on aspirin alone or in combination with clopidogrel. Clinical Trial Registration- URL: http://www.clinicaltrials.gov. Unique identifiers: NCT00799396 and NCT00370045.

摘要

背景——阿司匹林或阿司匹林与氯吡格雷联合的双重抗血小板治疗是心血管事件风险增加患者的标准治疗方法。然而,对阿司匹林(单独使用及与氯吡格雷联合使用)反应变异性的基因决定因素尚不清楚。

方法与结果——我们在抗血小板干预药物基因组学(PAPI)研究的个体(n = 565)中测量了双重抗血小板治疗前后的体外血小板聚集情况,并对药物反应进行了全基因组关联研究。通过在2个独立的阿司匹林治疗队列中检查基因型和心血管结局,扩展了重要发现:227例经皮冠状动脉介入治疗患者和国际维拉帕米缓释/群多普利研究(INVEST)基因亚组(INVEST-GENES)的1000例患者。全基因组关联研究结果显示,1q23染色体上的单核苷酸多态性与双重抗血小板治疗后的血小板聚集之间存在强关联。进一步的基因分型显示,血小板内皮聚集受体-1(PEAR1)基因中的rs12041331与双重抗血小板治疗反应最密切相关(P = 7.66×10⁻⁹)。在接受经皮冠状动脉介入治疗的白种人和黑人患者中,与GG纯合子相比,rs12041331的A等位基因携带者更有可能发生心血管事件或死亡(风险比分别为2.62;95%置信区间为0.96 - 7.10;P = 0.059;以及风险比为3.97;95%置信区间为1.10 - 14.31;P = 0.035)。在接受阿司匹林治疗的INVEST-GENES患者中,与GG纯合子相比,rs12041331的A等位基因携带者发生心肌梗死的风险显著增加(优势比为2.03;95%置信区间为1.01 - 4.09;P = 0.048)。

结论——PEAR1中的常见基因变异可能是单独使用阿司匹林或与氯吡格雷联合使用的患者血小板反应和心血管事件的决定因素。

临床试验注册——网址:http://www.clinicaltrials.gov。唯一标识符:NCT00799396和NCT00370045。

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