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血小板内皮聚集受体1基因变异的前瞻性评估揭示了阿司匹林对血小板聚集途径的依赖性作用。

Prospective Evaluation of Genetic Variation in Platelet Endothelial Aggregation Receptor 1 Reveals Aspirin-Dependent Effects on Platelet Aggregation Pathways.

作者信息

Backman J D, Yerges-Armstrong L M, Horenstein R B, Newcomer S, Shaub S, Morrisey M, Donnelly P, Drolet M, Tanner K, Pavlovich M A, O'Connell J R, Mitchell B D, Lewis J P

机构信息

Division of Endocrinology, Diabetes, and Nutrition, and Program for Personalized and Genomic Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.

Geriatrics Research and Education Clinical Center, Baltimore Veterans Administration Medical Center, Baltimore, Maryland, USA.

出版信息

Clin Transl Sci. 2017 Mar;10(2):102-109. doi: 10.1111/cts.12438. Epub 2017 Jan 11.

DOI:10.1111/cts.12438
PMID:28075528
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5355965/
Abstract

Genetic variation in the platelet endothelial aggregation receptor 1 (PEAR1) gene, most notably rs12041331, is implicated in altered on-aspirin platelet aggregation and increased cardiovascular event risk. We prospectively tested the effects of aspirin administration at commonly prescribed doses (81, 162, and 324 mg/day) on agonist-induced platelet aggregation by rs12041331 genotype in 67 healthy individuals. Prior to aspirin administration, rs12041331 minor allele carriers had significantly reduced adenosine diphosphate (ADP)-induced platelet aggregation compared with noncarriers (P = 0.03) but was not associated with other platelet pathways. In contrast, rs12041331 was significantly associated with on-aspirin platelet aggregation when collagen and epinephrine were used to stimulate platelet aggregation (P < 0.05 for all associations), but not ADP. The influence of PEAR1 rs12041331 on platelet aggregation is pathway-specific and is altered by aspirin at therapeutic doses, but not in a dose-dependent manner. Additional studies are needed to determine the impact of PEAR1 on cardiovascular events in aspirin-treated patients.

摘要

血小板内皮聚集受体1(PEAR1)基因的遗传变异,尤其是rs12041331,与阿司匹林治疗时血小板聚集改变及心血管事件风险增加有关。我们前瞻性地测试了常用处方剂量(81、162和324毫克/天)的阿司匹林对67名健康个体中rs12041331基因型激动剂诱导的血小板聚集的影响。在服用阿司匹林之前,rs12041331次要等位基因携带者与非携带者相比,二磷酸腺苷(ADP)诱导的血小板聚集显著降低(P = 0.03),但与其他血小板途径无关。相比之下,当使用胶原和肾上腺素刺激血小板聚集时,rs12041331与阿司匹林治疗时的血小板聚集显著相关(所有关联P < 0.05),但与ADP无关。PEAR1 rs12041331对血小板聚集的影响具有途径特异性,且在治疗剂量下会被阿司匹林改变,但并非呈剂量依赖性。需要进一步研究以确定PEAR1对阿司匹林治疗患者心血管事件的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f0/5355965/7a45fe3333d1/CTS-10-102-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f0/5355965/943c0b296f4d/CTS-10-102-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f0/5355965/33787bc360bc/CTS-10-102-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f0/5355965/7a45fe3333d1/CTS-10-102-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f0/5355965/943c0b296f4d/CTS-10-102-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f0/5355965/33787bc360bc/CTS-10-102-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/51f0/5355965/7a45fe3333d1/CTS-10-102-g003.jpg

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