Menopause and Alzheimer´s: a hormonal predilection

Frans Allinson Leiva-Cabrera, Emil Alejandro Moisupe-Agapito, Renzo Josue Nicolas-Montañez, Fernando José Lizardo Nuñez-Tapia, Mirtha Irene Oruna-Rondo, Angello D'sthefano Oyola-Azañero, Fabrizzio Ricardo Paredes-Ragas, Marcos Josue Paulino-Osorio
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Abstract

Alzheimer's disease (AD) is a syndrome related to the deterioration of cognitive functions such as language, thinking, attention, memory and calculation; due to the loss of neurons, synapse connections, the presence of senile plaques and neurofibrillary degeneration. For its part, menopause is defined as the permanent cessation of menstruation involving what was found in the respective review, two thirds of the population with Alzheimer's disease are female and of these, 60% are postmenopausal and over 60 years, since the main risk elements for the development of AD is the APOEε4 gene, located in the CNS responsible for producing astrocytes and microglia. ApoE, a protein encoded by the gene, affects the uptake and oligomerization of Aβ, making the elimination of Aβ less effective and accelerating aging, expressed in the reduction of T cells, especially in menopausal women carrying APOEε4, who are more susceptible to developing AD. The article aims to link Alzheimer's disease to menopause
更年期和老年痴呆症:荷尔蒙的偏好
阿尔茨海默病(AD)是一种与语言、思维、注意力、记忆和计算等认知功能退化有关的综合征;由于神经元丧失,突触连接,老年斑和神经原纤维变性的存在。就其本身而言,更年期被定义为月经的永久停止,涉及各自审查中发现的情况,患有阿尔茨海默病的人口中有三分之二是女性,其中60%是绝经后和60岁以上,因为AD发展的主要风险因素是APOEε4基因,位于中枢神经系统中负责产生星形胶质细胞和小胶质细胞。ApoE是一种由该基因编码的蛋白质,它影响a β的摄取和寡聚化,使a β的消除效果降低,加速衰老,表达为T细胞减少,特别是在携带APOEε4的绝经妇女中,她们更容易患AD。这篇文章旨在将阿尔茨海默病与更年期联系起来
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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