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Lack of an association between angiotensin-converting enzyme gene insertion/deletion polymorphism and ischaemic stroke.

TitleLack of an association between angiotensin-converting enzyme gene insertion/deletion polymorphism and ischaemic stroke.
Publication TypeJournal Article
Year of Publication2004
AuthorsKaragiannis, A., Balaska K., Tziomalos K., Tokalaki-Nikolaidou L., Papayeoryiou A., & Zamboulis C.
JournalEur Neurol
Volume51
Issue3
Pagination148-52
Date Published2004
ISSN0014-3022
KeywordsAged, Aged, 80 and over, Brain Ischemia, Case-Control Studies, DNA Mutational Analysis, Female, Gene Deletion, Genotype, Humans, Male, Middle Aged, Mutagenesis, Insertional, Peptidyl-Dipeptidase A, Polymerase Chain Reaction, Polymorphism, Genetic
Abstract

BACKGROUND AND PURPOSE: Numerous factors have been reported to influence the pathogenesis of stroke. The angiotensin I-converting enzyme (ACE) gene is a candidate gene for atherosclerotic-related diseases. In the present study, the association between the polymorphism of the ACE gene and ischaemic stroke was investigated.
METHODS: Using polymerase chain reaction techniques, 100 patients (48 males, age 69.3 +/- 9.7 years) with cerebral infarction and 100 age- and sex-matched controls were divided into the following three ACE genotypes [deletion (D) and insertion (I)]: II, ID and DD.
RESULTS: There was no evidence of any association between the ACE gene polymorphism and the presence of ischaemic stroke (odds ratio 0.874, 95% confidence interval 0.386-1.973).
CONCLUSIONS: The DD genotype in the human ACE gene does not appear to be a risk factor for ischaemic stroke. Further evaluation in a larger population study is required to examine the possibility of an increased risk of ischaemic stroke in DD homozygotes.

DOI10.1159/000077203
Alternate JournalEur. Neurol.
PubMed ID15007267

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