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Nature Versus Nurture: Does Proteostasis Imbalance Underlie the Genetic Environmental and Age-Related Risk Factors for Alzheimer’s Disease?

机译:自然与养育:蛋白质稳态失衡是阿尔茨海默氏病的遗传环境和与年龄相关的危险因素的基础吗?

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摘要

Aging is a risk factor for a number of “age-related diseases”, including Alzheimer’s disease (AD). AD affects more than a third of all people over the age of 85, and is the leading cause of dementia worldwide. Symptoms include forgetfulness, memory loss, and cognitive decline, ultimately resulting in the need for full-time care. While there is no cure for AD, pharmacological approaches to alleviate symptoms and target underlying causes of the disease have been developed, albeit with limited success. This review presents the age-related, genetic, and environmental risk factors for AD and proposes a hypothesis for the mechanistic link between genetics and the environment. In short, much is known about the genetics of early-onset familial AD (EO-FAD) and the central role played by the Aβ peptide and protein misfolding, but late-onset AD (LOAD) is not thought to have direct genetic causes. Nonetheless, genetic risk factors such as isoforms of the protein ApoE have been identified. Additional findings suggest that air pollution caused by the combustion of fossil fuels may be an important environmental risk factor for AD. A hypothesis suggesting that poor air quality might act by disrupting protein folding homeostasis (proteostasis) is presented.
机译:衰老是许多“与年龄有关的疾病”的风险因素,包括阿尔茨海默氏病(AD)。 AD影响85岁以上所有人群的三分之一以上,并且是全世界痴呆症的主要原因。症状包括健忘​​,记忆力减退和认知能力下降,最终导致需要全职护理。尽管无法治愈AD,但已经开发出缓解症状和靶向疾病根本原因的药理方法,尽管取得的成功有限。这篇综述介绍了与年龄相关的遗传,遗传和环境危险因素,并提出了遗传学与环境之间机械联系的假说。简而言之,关于家族性早发性AD(EO-FAD)的遗传学以及Aβ肽和蛋白质错误折叠所起的核心作用知之甚少,但是晚期性AD(LOAD)并没有直接的遗传原因。尽管如此,已经确定了遗传危险因素,例如蛋白ApoE的同工型。其他发现表明,由化石燃料燃烧引起的空气污染可能是AD的重要环境风险因素。提出了一个假说,认为不良的空气质量可能会通过破坏蛋白质折叠的稳态(蛋白稳态)而起作用。

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