2014
DOI: 10.3109/00207454.2013.879718
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Genetic polymorphism ofITGA2C807T can increase the risk of ischemic stroke

Abstract: The ITGA2 gene C807T polymorphism may be a susceptible predictor of the risk of ischemic stroke. More data are needed to elucidate the relationship further.

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Cited by 26 publications
(22 citation statements)
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“…76 A recent meta-analysis including 15 studies with a total number of 2242 cases and 2408 controls reported an association between the GPIa C807T polymorphism and risk of ischemic stroke in the overall population, in Asians and in the subgroup of hospitalized patients, but not in Caucasians and nonhospitalized individuals. 77 Croft et al 78 investigated 525 patients with acute MI and 474 controls and showed that the GPVI 13254CC genotype increased the risk of MI, particularly in patients aged 60 years and older (OR, 6.48; 95% CI, 1.47-28.45; P = 0.009). 78 Accordingly, Ollikainen et al, 79 investigated the association between the T13254C polymorphism of the GPVI gene and fatal MI and CAD in 300 men from the Helsinki Sudden Death Study (HSDS), reporting a significant association between the C-allele carriers (CT or CC) and coronary thrombosis.…”
Section: 54mentioning
confidence: 99%
“…76 A recent meta-analysis including 15 studies with a total number of 2242 cases and 2408 controls reported an association between the GPIa C807T polymorphism and risk of ischemic stroke in the overall population, in Asians and in the subgroup of hospitalized patients, but not in Caucasians and nonhospitalized individuals. 77 Croft et al 78 investigated 525 patients with acute MI and 474 controls and showed that the GPVI 13254CC genotype increased the risk of MI, particularly in patients aged 60 years and older (OR, 6.48; 95% CI, 1.47-28.45; P = 0.009). 78 Accordingly, Ollikainen et al, 79 investigated the association between the T13254C polymorphism of the GPVI gene and fatal MI and CAD in 300 men from the Helsinki Sudden Death Study (HSDS), reporting a significant association between the C-allele carriers (CT or CC) and coronary thrombosis.…”
Section: 54mentioning
confidence: 99%
“…In contrary to Nikolopoulos' reports, it revealed that ITGA2 rs1126643 polymorphism could amplify the risk of ischemic stroke in the overall population, Asians and the group of hospital-based patients. However, it is notable that statistical association was not found in Caucasians and nonhospitalized subjects [48]. Xin et al, on the other hand, performed a meta-analysis that comprised four studies focused on the presence of rs1126643 poly morphism in young ischemic stroke patients and did not find any significant associations (Table 2) [49].…”
Section: Gpia/iia -Itga2 and Itgb1 Genesmentioning
confidence: 97%
“…Таким чином, за умов пошкодження атеросклеротич-ної бляшки, що є основною складовою етіопатогенезу ГКС, тромбоцити пацієнтів з Т/Т генотипом вияв-ляються надзвичайно чутливими до колагену субендотеліального прошарку, який оголюється. Слід зазначити, що у про-ведених раніше дослідженнях вказувалось на вищий ризик розвитку ішемічного інсульту у пацієнтів з Т/Т генотипом [11], а також вищі рівні холестерину, ліпопротеїдів низької щільності, що разом із збільшеною агрега-цією тромбоцитів та їх підви-щеною чутливістю до колагену може пояснювати віднесення Т/Т генотипу до ризик факторів ви-никнення тромботичних подій у хворих із серцевою патологією.…”
Section: обговорення результатів дослідженняunclassified