Influence of Variation in the Follicle-Stimulating Hormone Receptor Gene (FSHR) and Age at Menopause on the Development of Alzheimer's Disease in Women

被引:28
|
作者
Corbo, Rosa Maria [1 ,2 ]
Gambina, Giuseppe [3 ,4 ]
Broggio, Elisabetta [3 ,4 ]
Scacchi, Renato [2 ]
机构
[1] Univ Roma La Sapienza, Dept Biol & Biotechnol, IT-00185 Rome, Italy
[2] CNR Inst Mol Biol & Pathol, Rome, Italy
[3] Univ Verona, Dept Neurosci, Alzheimers Dis & Other Dementias Ctr, I-37100 Verona, Italy
[4] Hosp Verona, Verona, Italy
关键词
Alzheimer's disease; Fertility; FSHR genotypes; Menopausal age; Women; APOLIPOPROTEIN-E; GENDER-DIFFERENCES; NATURAL MENOPAUSE; CYP19; AROMATASE; POLYMORPHISMS; RISK; DEMENTIA; ONSET; ASSOCIATION; FECUNDITY;
D O I
10.1159/000330472
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Background: The higher prevalence of sporadic Alzheimer's disease (AD) in women may be explained by their longer life expectancy, but also by biological gender-specific factors such as a woman's past fertility. Methods: We investigated the relationship between fertility and susceptibility to AD in women by studying two polymorphisms at codons 307 and 680 of the follicle-stimulating hormone receptor gene (FSHR) involved in determining human fertility. The role of age at menopause (AM) as a gender-specific AD susceptibility determinant was also examined. The study population comprised 291 AD patients (70.1% women) and 134 controls (63.4% women). Results: Logistic regression analysis showed that only among the women the FSHR AS/AS genotype was associated with a significantly lower risk of AD (OR = 0.36, 95% CI: 0.15-0.85), suggesting a gender-specific protective role of the FSHR genotype against AD susceptibility. A lower age at natural menopause was observed in the AD patients (49.7 +/- 2.53) than in the controls (50.7 +/- 2.53, p = 0.02) and on linear regression analysis an association emerged between an earlier AM and an earlier AD onset (p = 0.004). Conclusions: Genetic and non-genetic gender-specific factors may contribute to the AD pathogenesis in women, although further investigations are required to clarify their actual role. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:63 / 69
页数:7
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