Abstract
Retrospective analysis shows that women who took estrogen replacement therapy may have less risk of cognitive decline and of developing Alzheimer's disease (AD). The greater risk associated with female gender and these observations suggest that estrogen may be implicated in the aetiology of AD. Estrogen is one of a family of sex steroids that exerts many of its genomic effects through the activation of the nuclear estrogen receptors, ER alpha and ER beta. Previously, increased risk for AD has been reported for polymorphisms in the ER alpha gene in a Japanese cohort, however, this association has not been systematically replicated. We have further investigated polymorphisms in the ER alpha and have extended this to investigate an association with a polymorphism within the ER beta gene in an independent UK Caucasian population. We found no independent association of these polymorphisms with the risk of developing AD in the total sample nor within either gender. However, we did detect a significant interaction between the ER alpha and ER beta polymorphisms and the risk for AD (OR = 0.22 95% CI (0.05-0.88), P = 0.02). If this finding can be supported in other independent studies, it may suggest that the risk for AD may be modulated only when both ER alpha and ER beta have particular variations in their expression and/or biological activities. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
Original language | English |
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Pages (from-to) | 193-197 |
Number of pages | 4 |
Journal | Neuroscience Letters |
Volume | 306 |
Issue number | 3 |
Early online date | 8 Jun 2001 |
DOIs | |
Publication status | Published - 29 Jun 2001 |
Keywords
- Alzheimer's disease
- estrogen receptor
- polymorphisms
- Alpha gene polymorphisms
- association
- risk
- age
- increases
- women
- APOE