Kazama Hirohito, Ruberu Nyoka N, Murayama Shigeo, Saito Yuko, Nakahara Ken-Ichi, Kanemaru Kazutomi, Nagura Hiroshi, Arai Tomio, Sawabe Motoji, Yamanouchi Hiroshi, Orimo Hajime, Hosoi Takayuki
Department of Endocrinology, Tokyo Metropolitan Institute of Gerontology, Tokyo, Japan.
Dement Geriatr Cogn Disord. 2004;18(2):145-50. doi: 10.1159/000079194. Epub 2004 Jun 18.
Estrogen receptor alpha (ERalpha) may be implicated in the pathogenesis of Alzheimer's disease (AD). The aim of this study was to clarify the association between ERalpha gene polymorphisms and AD-related pathologic changes. The staging of neurofibrillary tangles (NFT) and senile plaques (SP) was performed according to the method by Braak and Braak and two polymorphisms, PvuII (P or p) and XbaI (X or x), of the ERalpha gene were typed in 551 Japanese cadavers (294 men and 257 women; mean age, 80.8 years). Distributions of the NFT and SP stages significantly correlated with age (NFT: r = 0.306, p < 0.0001; SP: r = 0.237, p < 0.0001) and were significantly higher in patients with the apolipoprotein E epsilon4 allele (p < 0.0001). Possession of the P allele showed a trend to be associated with a more serious NFT stage, but had no relationship with the SP stage. In men, a significant association between PvuII polymorphism and the NFT stage (p = 0.002) was found, revealing a gene- dose effect of the P allele. Similar results were obtained in the men without the epsilon4 allele (p = 0.011). Multiple regression analyses demonstrated that age was the strongest determinant of the NFT stage, possession of the epsilon4 allele was the next strongest, and PvuII polymorphism was the third strongest (p < 0.0001, R(2) = 0.144). The XbaI polymorphism did affect neither the NFT stage nor the SP stage. In conclusion, the PvuII polymorphism of the ERalpha gene is associated with Braak NFT stages and possession of the P allele may act as a risk factor for AD in Japanese men, especially in those without the epsilon4 allele.
雌激素受体α(ERα)可能与阿尔茨海默病(AD)的发病机制有关。本研究的目的是阐明ERα基因多态性与AD相关病理变化之间的关联。根据Braak和Braak的方法对神经原纤维缠结(NFT)和老年斑(SP)进行分期,并对551例日本尸体(294名男性和257名女性;平均年龄80.8岁)的ERα基因的两种多态性,即PvuII(P或p)和XbaI(X或x)进行分型。NFT和SP分期的分布与年龄显著相关(NFT:r = 0.306,p < 0.0001;SP:r = 0.237,p < 0.0001),并且在载脂蛋白E ε4等位基因的患者中显著更高(p < 0.0001)。携带P等位基因显示出与更严重的NFT分期相关的趋势,但与SP分期无关。在男性中,发现PvuII多态性与NFT分期之间存在显著关联(p = 0.002),揭示了P等位基因的基因剂量效应。在没有ε4等位基因的男性中也获得了类似的结果(p = 0.011)。多元回归分析表明,年龄是NFT分期的最强决定因素,携带ε4等位基因是第二强因素,PvuII多态性是第三强因素(p < 0.0001,R(2) = 0.144)。XbaI多态性既不影响NFT分期也不影响SP分期。总之,ERα基因的PvuII多态性与Braak NFT分期相关,并且携带P等位基因可能是日本男性AD的危险因素,尤其是在那些没有ε4等位基因的男性中。