GENETICS OF STROKE IN 21 st CENTRY - SciReNe
GENETICS OF STROKE IN 21 st CENTRY - SciReNe
GENETICS OF STROKE IN 21 st CENTRY - SciReNe
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Khalil Hamzi<br />
the development of IS in Northern Han Chinese. Brain Research BulletinVolume 81, Issue 1,<br />
15 January 2010, Pages 38-42 Nan Li 1, a, Zhiyi He, Jialiang Xu2, Fang Liu3, a, Shumin<br />
Deng4, a, and Hui Zhang5. It remains difficult to conclude whether or not the association and<br />
the role of the PDE4D gene in the pathogenesis of DALYs. In fact we have few <strong>st</strong>udies, and<br />
they are limited to a small number of patients. It would be intere<strong>st</strong>ing to <strong>st</strong>udy larger series of<br />
different populations.Therefore, experimental <strong>st</strong>udies on the function of PDE4D help to unveil<br />
the my<strong>st</strong>ery. PDE4D is a large family of PDE, which are the cAMP hydrolytic enzymes and<br />
key molecules of signal transduction in several cell types, including smooth muscle cells of<br />
blood vessels. These findings also apply to ALOX5AP (5 - lipoxygenaseactivatingprotein)<br />
involved in the process of vascular inflammation which gives this gene of particular intere<strong>st</strong><br />
mainly in its synergy with the processor of atherosclerosis (ElinLõhmussaar, and the Gene<br />
ALOX5AP PDE4D Gene in a Central European Population of Stroke Patients, 2005).<br />
i- "5-lipoxygenase-activating proteingene" gene (ALOX5AP) A second positive<br />
relationship étudeIslandaise of <strong>st</strong>roke was introduced in 2004, it showed that the locus13q12<br />
13e<strong>st</strong>-linked gene with both myocardial infarction and cerebral infarction / TIA (Helgadottir<br />
A, 2004). In this chromosomal region is the gene ALOX5AP involved in the metabolism of<br />
leukotrienes, thus in atherosclerosis. The sequencing of the gene ALOX5AP revealed the<br />
presence of SNP haplotype (HAPA), associated with a risk two times higher in ischemic<br />
<strong>st</strong>roke and hemorrhagic. These results were répliquédans a Scottish <strong>st</strong>udy (Helgadottir A,<br />
2005) and has not been found in a <strong>st</strong>udy of 640 American and 97% white (Meschia JF, 2005).<br />
j-Other candidate genes and pathways other candidate genes have been <strong>st</strong>udied for<br />
possible association with ischemic <strong>st</strong>roke. They are li<strong>st</strong>ed in the webtable or discussed in<br />
reviews. Among these genes, those involved in inflammation such as l'interleukine 1,<br />
interleukin 6, TNF, Toll-likereceptor 4, P-selectin and E-selectin, C-reactive protein in lipid<br />
metabolism such as apolipoprotein E, paraoxonase, epoxy), the release of nitric oxide. In mo<strong>st</strong><br />
cases, however, the results were negative or could not be replicated in future <strong>st</strong>udies.<br />
IDBM<br />
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