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Genetics of stroke: a review of recent advances.

Authors
Type
Published Article
Journal
Expert Review of Molecular Diagnostics
1744-8352
Publisher
Informa UK (Taylor & Francis)
Publication Date
Volume
8
Issue
4
Pages
495–513
Identifiers
DOI: 10.1586/14737159.8.4.495
PMID: 18598230
Source
Medline
License
Unknown

Abstract

Stroke is a multifactorial disease responsible for nearly 10% of deaths each year in industrialized countries. While some monogenic forms of stroke have been described, the vast majority result from the common polygenic form of the disease. Progress in molecular genetics has allowed the identification, through genome-wide linkage analysis, of various candidate genes, including the genes encoding PDE4D and ALOX5AP. Since then, genetic research has been extensively performed from single candidate genes to whole-genome scan studies, in parallel with the development of high-throughput technologies in molecular diagnostics. Additionally, the safety and efficacy of tissue plasminogen activator, the only approved therapy for the acute phase of stroke, is modulated by genetic background associated with the occurrence of hemorrhagic transformations and with the revascularization of the cerebral arteries. In the near future, understanding the contribution of stroke genetic factors will lead to improvements in prevention and treatments for neurovascular diseases.

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