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 BRIEF REPORT
Year : 2009  |  Volume : 57  |  Issue : 5  |  Page : 636--637

Prevalence of prothrombotic polymorphisms in a selected cohort of cryptogenic and noncryptogenic ischemic stroke patients


1 IRCCS Centro Neurolesi "Bonino-Pulejo", Italy
2 Dipartimento di Neuroscienze, Policlinico Universitario, Messina, Italy
3 U.O. Genetica, Ospedali Riuniti di Reggio di Calabria, Italy

Correspondence Address:
Rocco Salvatore Calabro
IRCCS Centro Neurolesi, "Bonino Pulejo", S.S.113 via Palermo, Cda Casazza, 98124 Messina
Italy
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0028-3886.57819

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Ischemic stroke is a complex multifactorial disease and approximately 30%, especially in the young, are cryptogenic. In some of the patients with cryptogenic ischemic stroke the underlying risk factor may be a prothrombotic state. We studied 101 patients with ischemic stroke under 55 years of age. All the patients underwent an extensive diagnostic evaluation to determine the cause of stroke. Common variations in the genes encoding factor V, prothrombin, 5,10-methylenetetrahydrofolate reductase, plasminogen activator inhibitor-1, and human platelet alloantigens-1 were evaluated. Of the 101 patients with ischemic stroke, 28 patients had cryptogenic ischemic stroke. At least one of the different genetic polymorphisms investigated was present in 44% patients in the total group and in 48% of patients with cryptogenic ischemic stroke. In this study population under 55 years of age there was no significant difference in the prevalence of various genetic polymorphisms, factor V, prothrombin, 5,10-methylenetetrahydrofolate reductase, plasminogen activator inhibitor-1, and human platelet alloantigens) in patients with cryptogenic ischemic stroke and in patients with ischemic stroke of determined cause.






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