[1]GBD 2019 Stroke Collaborators. Global, regional, and national burden of stroke and its risk factors, 1990-2019: a systematic analysis for the Global Burden of Disease Study 2019[J]. Lancet Neurol, 2021, 20(10): 795-820.
[2]Ma Q F, Li R, Wang L J, et al. Temporal trend and attributable risk factors of stroke burden in China, 1990-2019: an analysis for the Global Burden of Disease Study 2019[J]. Lancet Public Health, 2021, 6(12): e897-e906.
[3]Bergmark B A, Mathenge N, Merlini P A, et al. Acute coronary syndromes[J]. Lancet, 2022, 399(10332): 1347-1358.
[4]Xian Y, Xu H L, Matsouaka R, et al. Analysis of prescriptions for dual antiplatelet therapy after acute ischemic stroke[J]. JAMA Netw Open, 2022, 5(7): e2224157.
[5]Simonte G, Guglielmini G, Falcinelli E, et al. High-on-treatment platelet reactivity predicts adverse outcome after carotid artery stenting: a prospective study[J]. Thromb Res, 2023, 222: 117-123.
[6]Shah J, Liu S M, Yu W G. Contemporary antiplatelet therapy for secondary stroke prevention: a narrative review of current literature and guidelines[J]. Stroke Vasc Neurol, 2022, 7(5): 406-414.
[7]Khan H, Kanny O, Syed M H, et al. Aspirin resistance in vascular disease: a review highlighting the critical need for improved point-of-care testing and personalized therapy[J]. Int J Mol Sci, 2022, 23(19):11317.
[8]Patel S, Arya V, Saraf A, et al. Aspirin and clopidogrel resistance in Indian patients with ischemic stroke and its associations with gene polymorphisms: a pilot study[J]. Ann Indian Acad Neurol, 2019, 22(2): 147-152.
[9]Ross S, Krebs K, Pare G, et al. Pharmacogenomics in stroke and cardiovascular disease: state of the art[J]. Stroke, 2023, 54(1): 270-278.
[10]Montinari M R, Minelli S, De Caterina R. The first 3500 years of aspirin history from its roots-a concise summary[J]. Vascul Pharmacol, 2019, 113: 1-8.
[11]Li X Q, Ma N, Li X G, et al. Association of PON1, P2Y12 and COX1 with recurrent ischemic events in patients with extracranial or intracranial stenting[J]. PLoS One, 2016, 11(2): e0148891.
[12]Zhao Z G, Li X G, Sun S S, et al. Impact of genetic polymorphisms related to clopidogrel or acetylsalicylic acid pharmacology on clinical outcome in Chinese patients with symptomatic extracranial or intracranial stenosis[J]. Eur J Clin Pharmacol, 2016, 72(10): 1195-1204.
[13]Pereira N L, Rihal C S, So D, et al. Clopidogrel pharmacogenetics[J]. Circ Cardiovasc Interv, 2019, 12(4): e007811.
[14]Saiz-Rodríguez M, Belmonte C, Caniego J L, et al. Influence of CYP450 enzymes, CES1, PON1, ABCB1, and P2RY12 polymorphisms on clopidogrel response in patients subjected to a percutaneous neurointervention[J]. Clin Ther, 2019, 41(6): 1199-1212.e2.
[15]Pan Y S, Elm J J, Li H, et al. Outcomes associated with clopidogrel-aspirin use in minor stroke or transient ischemic attack: a pooled analysis of clopidogrel in high-risk patients with acute non-disabling cerebrovascular events (CHANCE) and platelet-oriented inhibition in new TIA and minor ischemic stroke (POINT) trials[J]. JAMA Neurol, 2019, 76(12): 1466-1473.
[16]Brown T, Gonzales N. Optimizing choice of dual antiplatelet therapy in CYP2C19 loss-of-function carriers[J]. Neurology, 2023, 100(5): 223-224.
[17]Yip V L M, Pirmohamed M. Expanding role of pharmacogenomics in the management of cardiovascular disorders[J]. Am J Cardiovasc Drugs, 2013, 13(3): 151-162.
[18]Jackson S P. Arterial thrombosis-insidious, unpredictable and deadly[J]. Nat Med, 2011, 17(11): 1423-1436.
[19]Kunicki T J, Orchekowski R, Annis D, et al. Variability of integrin alpha 2 beta 1 activity on human platelets[J]. Blood, 1993, 82(9): 2693-2703.[20]Deckmyn H, Chew S L, Vermylen J. Lack of platelet response to collagen associated with an autoantibody against glycoprotein IA: a novel cause of acquired qualitative platelet dysfunction[J]. Thromb Haemost, 1990, 64: 74-79.
[21]Huang X Y, Fu W J, Mei Z Z, et al. Association between platelet glycoprotein Ia C807T gene polymorphism and ischemic stroke: a meta-analysis in a separate ethnic group[J]. Cell Mol Biol, 2017, 63(11): 111-115.
[22]Liu H, Wang Y, Zheng J, et al. Platelet glycoprotein gene Ia C807T, HPA-3, and Ibα VNTR polymorphisms are associated with increased ischemic stroke risk: evidence from a comprehensive meta-analysis[J]. Int J Stroke, 2017, 12(1): 46-70.
[23]De Oliveira M H, André C, Spector N, et al. 807C/T polymorphism in the platelet glycoprotein Ia gene in young patients with ischemic stroke of undetermined etiology[J]. Blood Coagul Fibrinolysis, 2007, 18(7): 599-602.
[24]Nikolopoulos G K, Tsantes A E, Bagos P G, et al. Integrin, alpha 2 gene C807T polymorphism and risk of ischemic stroke: a meta-analysis[J]. Thromb Res, 2007, 119(4): 501-510.
[25]Dodson P M, Haynes J, Starczynski J, et al. The platelet glycoprotein Ia/IIa gene polymorphism C807T/G873A: a novel risk factor for retinal vein occlusion[J]. Eye, 2003, 17(6): 772-777.
[26]Wu G L, Xi Y J, Yao L, et al. Genetic polymorphism of ITGA2 C807T can increase the risk of ischemic stroke[J]. Int J Neurosci, 2014, 124(11): 841-851.
[27]Lloyd-Jones D, Adams R J, Brown T M, et al. Executive summary: heart disease and stroke statistics—2010 update: a report from the American Heart Association[J]. Circulation, 2010, 121(7): 948-954.
[28]Lewis J P, Ryan K, O'Connell J R, et al. Genetic variation in PEAR1 is associated with platelet aggregation and cardiovascular outcomes[J]. Circ Cardiovasc Genet, 2013, 6(2): 184-192.
|