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阿尔茨海默病源于早期生活中的失调微生物组。

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

机构信息

Center for Dementia Research, Nathan Kline Institute, Orangeburg, New York.

Department of Psychiatry.

出版信息

J Infect Dis. 2024 Sep 10;230(Supplement_2):S141-S149. doi: 10.1093/infdis/jiae200.

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.

摘要

阿尔茨海默病(AD)是一种神经退行性疾病,治疗选择有限。因此,需要新的预防和治疗方法。一个重点是人类微生物组,即生活在我们体内和体表的微生物群落,它有助于人类的免疫、代谢和认知发育,并可能在神经退行性变中发挥机制作用。AD 和与 AD 相关的痴呆症(ADRD)被认为是具有复杂病理生物学的谱系障碍。AD/ADRD 的发病始于明显的临床症状之前,但启动触发因素仍未确定。我们假设,生命早期正常肠道微生物组的破坏会导致隔海马和皮质脑回路内的病理级联反应。我们建议进行研究,以了解生命早期微生物组的变化如何导致既定的 AD/ADRD 模型中的 AD 标志性病理学。具体来说,我们假设生命早期接触抗生素会导致类似 AD 的疾病表型加剧,而这些表型可能可以通过特定的微生物干预来治疗。我们提出了适合测试这些假设的模型。

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