Estrogen receptor beta (ESR2) gene polymorphism and susceptibility to dementia
Strong evidence supports the involvement of sex steroid hormones in the development and progression of dementia. Attention has been largely focused on the association between genetic variants of estrogen receptor alpha (ERα , ESR1 ) with dementia, although several studies indicate that ERβ is predom...
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Published in | Acta neurologica Belgica Vol. 121; no. 5; pp. 1281 - 1293 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
Cham
Springer International Publishing
01.10.2021
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Subjects | |
Online Access | Get full text |
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Summary: | Strong evidence supports the involvement of sex steroid hormones in the development and progression of dementia. Attention has been largely focused on the association between genetic variants of estrogen receptor alpha (ERα
, ESR1
) with dementia, although several studies indicate that ERβ is predominantly expressed in the brain. Interestingly, however, a limited number of studies evaluate the role of ERβ (
ESR2
) in dementia. Therefore, a meta-analysis was conducted to clarify the association between
ESR2
genetic polymorphisms and the risk of dementia. All the relevant studies evaluating
ESR2
genetic polymorphisms and dementia were identified through online databases. In total, 14 studies including 20,609 subjects were analyzed. Collectively, it was found that a combined data set of
ESR2
polymorphisms was not associated with dementia risk. Interestingly,
ESR2
rs4986938 polymorphism is significantly associated with dementia in the Asian population (OR = 0.73, 95% CI 0.59–0.91,
P
= 0.006). The carrier of A allele in rs4986938 exhibits a protective effect against dementia (A vs. G, OR = 0.6633,
P
= 0.012; AA + GA vs. GG, OR = 0.6499,
P
= 0.014; GA vs. AA + GG, OR = 0.6672,
P
= 0.025; GA vs. GG, OR = 0.6617,
P
= 0.022). In conclusion, our study suggests that
ESR2
genetic polymorphisms are not significantly associated with dementia risk.
ESR2
rs4986938 may have potential as a genetic marker for dementia in the Asian population. However, further studies need to verify this conclusion. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0300-9009 2240-2993 2240-2993 |
DOI: | 10.1007/s13760-020-01360-z |