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Phosphodiesterase 4D and 5-lipoxygenase activating protein genes and risk of ischemic stroke in Sardinians
Authors:Giovanni Quarta  Rosita Stanzione  Anna Evangelista  Bastianina Zanda  Emanuele Di Angelantonio  Simona Marchitti  Sara Di Castro  Marta Di Vavo  Massimo Volpe  and Speranza Rubattu
Institution:1Department of Cardiology, IInd School of Medicine, University La Sapienza, Ospedale Sant''Andrea, Rome;2IRCCS Neuromed, Polo Molisano University La Sapienza of Rome, Pozzilli (Is), Italy;3Department of Neurology, University of Sassari, Sassari, Italy;4Department of Public Health and Primary Care, University of Cambridge, Cambridge, England, UK
Abstract:Genetic factors contribute to the risk of ischemic stroke (IS). The phosphodiesterase-4D (PDE4D) and the 5-lipoxygenase activating protein (ALOX5AP) genes were identified as contributors to stroke in an Icelandic population. In an attempt to better define the contributory role of PDE4D and ALOX5AP genes to the risk of IS in humans, we carried out the present association study in a well-characterized, earlier published, genetically homogenous population from the island of Sardinia, Italy. In this cohort, including 294 cases and 235 controls, age, hypertension, hypercholesterolemia, and atrial fibrillation represent risk factors for IS. The PDE4D gene was evaluated by four single nucleotide polymorphisms (SNP32, SNP45, SNP83, SNP87) and by the microsatellite AC008818-1; the ALOX5AP gene was characterized by three SNPs (SG13S32, SG13S89, ALO2A). The results of our study provide no evidence of association between any single PDE4D and ALOX5AP gene variant with the risk of IS in the Sardinian cohort. Haplotype analysis, including that constructed with allele 0 of microsatellite AC008818-1 and SNP45 of the PDE4D gene, was also negative. In conclusion, we found no evidence of association between PDE4D and ALOX5AP genes and the risk of IS in a genetically homogenous population from Sardinia.
Keywords:phosphodiesterase 4D  5-lipoxygenase activating protein  ischemic stroke
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