Alzheimer's Disease Has Its Origins in Early Life via a Perturbed Microbiome.

Stephen D Ginsberg,Martin J Blaser
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Abstract

Alzheimer's disease (AD) is a neurodegenerative disorder with limited therapeutic options. Accordingly, new approaches for prevention and treatment are needed. One focus is the human microbiome, the consortium of microorganisms that live in and on us, which contributes to human immune, metabolic, and cognitive development and that may have mechanistic roles in neurodegeneration. AD and Alzheimer's disease-related dementias (ADRD) are recognized as spectrum disorders with complex pathobiology. AD/ADRD onset begins before overt clinical signs, but initiation triggers remain undefined. We posit that disruption of the normal gut microbiome in early life leads to a pathological cascade within septohippocampal and cortical brain circuits. We propose investigation to understand how early-life microbiota changes may lead to hallmark AD pathology in established AD/ADRD models. Specifically, we hypothesize that antibiotic exposure in early life leads to exacerbated AD-like disease endophenotypes that may be amenable to specific microbiological interventions. We propose suitable models for testing these hypotheses.
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阿尔茨海默病起源于生命早期微生物群紊乱
阿尔茨海默病(AD)是一种神经退行性疾病,治疗方法有限。因此,需要新的预防和治疗方法。其中一个重点是人类微生物组,即生活在我们体内和身上的微生物联合体,它有助于人类免疫、代谢和认知能力的发展,并可能在神经退行性变中发挥机理作用。注意力缺失症和阿尔茨海默病相关痴呆症(ADRD)被认为是病理生物学复杂的谱系障碍。AD/ADRD 在出现明显临床症状之前就已发病,但发病诱因仍未确定。我们认为,生命早期正常肠道微生物群的破坏会导致隔海马和大脑皮层回路中的病理级联。我们建议进行调查,以了解生命早期微生物群的变化如何导致已建立的 AD/ADRD 模型中的标志性 AD 病理学。具体来说,我们假设生命早期的抗生素暴露会导致类似于 AD 的疾病内表型加剧,而这些内表型可能适合特定的微生物干预措施。我们提出了测试这些假设的合适模型。
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