Resumen
To investigate the possible involvement of the transferrin (TF) gene polymorphism in the manifestation of Alzheimer's disease (AD), we analyzed the TF and apolipoprotein E (APOE) genotypes of 67 sporadic late-onset AD patients and 131 normal elderly controls in the Chinese population. Our data showed that the TF C1 homozygosity carriers had an increased risk of AD in subjects ≥75 years of age, showing that homozygosity for the TF C1 allele was associated with an approximately three-fold increased risk (OR=3.57, 95% CI, 1.24-10.27, P=0.014). No synergic effects were found between the APOE ε4 allele and TF gene polymorphisms.
Idioma original | English (US) |
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Páginas (desde-hasta) | 209-211 |
Número de páginas | 3 |
Publicación | Neuroscience Letters |
Volumen | 349 |
N.º | 3 |
DOI | |
Estado | Published - oct 9 2003 |
Publicado de forma externa | Sí |
ASJC Scopus subject areas
- General Neuroscience