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Analysis of the relationship between the gut microbiome and dementia: a cross-sectional study conducted in Japan

机译:肠道微生物组与痴呆之间的关系分析:在日本进行的横断面研究

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Dysregulation of the gut microbiome is associated with several life-threatening conditions and thus might represent a useful target for the prevention of dementia. However, the relationship between the gut microbial population and dementia has not yet been fully clarified. We recruited outpatients visiting our memory clinic to participate in this study. Information on patient demographics, risk factors, and activities of daily living was collected, and cognitive function was assessed using neuropsychological tests and brain magnetic resonance imaging scans. Faecal samples were obtained, and the gut microbiome was assessed by terminal restriction fragment length polymorphism (T-RFLP) analysis, one of the most well-established and reliable 16S ribosomal RNA-based methods for classifying gut microbiota. Patients were divided into two groups, demented and non-demented. Multivariable logistic regression models were used to identify the variables independently associated with dementia. The T-RFLP analysis revealed differences in the composition of the gut microbiome: the number of Bacteroides (enterotype I) was lower and the number of 'other' bacteria (enterotype III) was higher in demented than non-demented patients. Multivariable analyses showed that the populations of enterotype I and enterotype III bacteria were strongly associated with dementia, independent of the traditional dementia biomarkers. Further studies of the metabolites of gut microbes are needed to determine the mechanism underlying this association.
机译:肠道微生物组的失调与几种危及生命的疾病有关,因此可能代表了预防痴呆的有用靶标。但是,肠道微生物数量与痴呆之间的关系尚未完全阐明。我们招募了门诊患者前往我们的记忆诊所参加这项研究。收集有关患者人口统计学,危险因素和日常生活活动的信息,并使用神经心理学测试和脑磁共振成像扫描评估认知功能。获得粪便样品,并通过末端限制性片段长度多态性(T-RFLP)分析评估肠道微生物组,这是最完善,最可靠的基于16S核糖体RNA的肠道微生物群分类方法之一。患者分为痴呆和非痴呆两组。使用多变量逻辑回归模型来识别与痴呆症独立相关的变量。 T-RFLP分析显示肠道微生物组的组成存在差异:与非痴呆患者相比,痴呆患者中的拟杆菌含量较低(I型实体),“其他”细菌数量(III型实体)较高。多变量分析显示,肠型I和肠型III细菌的种群与痴呆症密切相关,独立于传统的痴呆症生物标志物。需要进一步研究肠道微生物的代谢产物,以确定这种关联的基础。

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