Abstract | OBJECTIVE: METHODS: In the present study, we examined whether the LGALS2 3279TT homozygote variant alone can influence the prevalence of ischaemic stroke, and whether it can interact somehow with the disadvantageous LTA 252GG homozygote variant. Genetic and clinical data of 385 ischemic stroke patients and 303 stroke and neuroimaging alteration-free controls were analysed. RESULTS: The combination of the LGALS2 3279TT and LTA 252GG homozygote was significantly less frequent in the ischemic stroke group (1.56%) than in the controls (5.94%, p<0.00187; overall stroke group: crude OR: 0.25, 95% CI: 0.1-0.64; adjusted OR: 0.03, 95% CI: 0.025-0.71). CONCLUSIONS: This finding suggests a gene-gene interaction.
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Authors | Zoltan Szolnoki, Anita Maasz, Lili Magyari, Katalin Horvatovich, Bernadett Farago, Andras Kondacs, Anita Bodor, Ferenc Hadarits, Peter Orosz, Alexandru Ille, Bela Melegh |
Journal | Clinical neurology and neurosurgery
(Clin Neurol Neurosurg)
Vol. 111
Issue 3
Pg. 227-30
(Apr 2009)
ISSN: 1872-6968 [Electronic] Netherlands |
PMID | 19013708
(Publication Type: Journal Article)
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Chemical References |
- Galectin 2
- Lymphotoxin-alpha
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Topics |
- Adult
- Aged
- Aged, 80 and over
- Brain Ischemia
(diagnosis, genetics)
- Female
- Galectin 2
(genetics)
- Gene Frequency
- Genetic Predisposition to Disease
- Homozygote
- Humans
- Lymphotoxin-alpha
(genetics)
- Magnetic Resonance Imaging
- Male
- Middle Aged
- Polymerase Chain Reaction
- Polymorphism, Restriction Fragment Length
- Risk Factors
- Stroke
(diagnosis, genetics)
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