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帕金森病中的肠道微生物群:对疾病进展影响及设备辅助治疗应用的纵向研究

The Gut Microbiome in Parkinson's Disease: A Longitudinal Study of the Impacts on Disease Progression and the Use of Device-Assisted Therapies.

作者信息

Lubomski Michal, Xu Xiangnan, Holmes Andrew J, Muller Samuel, Yang Jean Y H, Davis Ryan L, Sue Carolyn M

机构信息

Department of Neurology, Royal North Shore Hospital, St Leonards, NSW, Australia.

Department of Neurogenetics, Kolling Institute, Faculty of Medicine and Health, University of Sydney, St Leonards, NSW, Australia.

出版信息

Front Aging Neurosci. 2022 May 17;14:875261. doi: 10.3389/fnagi.2022.875261. eCollection 2022.

Abstract

BACKGROUND

Altered gut microbiome (GM) composition has been established in Parkinson's disease (PD). However, few studies have longitudinally investigated the GM in PD, or the impact of device-assisted therapies.

OBJECTIVES

To investigate the temporal stability of GM profiles from PD patients on standard therapies and those initiating device-assisted therapies (DAT) and define multivariate models of disease and progression.

METHODS

We evaluated validated clinical questionnaires and stool samples from 74 PD patients and 74 household controls (HCs) at 0, 6, and 12 months. Faster or slower disease progression was defined from levodopa equivalence dose and motor severity measures. 19 PD patients initiating Deep Brain Stimulation or Levodopa-Carbidopa Intestinal Gel were separately evaluated at 0, 6, and 12 months post-therapy initiation.

RESULTS

Persistent underrepresentation of short-chain fatty-acid-producing bacteria, , and , were apparent in PD patients relative to controls. A sustained effect of DAT initiation on GM associations with PD was not observed. PD progression analysis indicated that the genus was underrepresented in faster progressing PD patients at = 0 and = 12 months. Two-stage predictive modeling, integrating microbiota abundances and nutritional profiles, improved predictive capacity (change in Area Under the Curve from 0.58 to 0.64) when assessed at Amplicon Sequence Variant taxonomic resolution.

CONCLUSION

We present longitudinal GM studies in PD patients, showing persistently altered GM profiles suggestive of a reduced butyrogenic production potential. DATs exerted variable GM influences across the short and longer-term. We found that specific GM profiles combined with dietary factors improved prediction of disease progression in PD patients.

摘要

背景

帕金森病(PD)患者的肠道微生物群(GM)组成已发生改变。然而,很少有研究对PD患者的GM进行纵向研究,或研究器械辅助治疗的影响。

目的

研究接受标准治疗的PD患者以及开始器械辅助治疗(DAT)的患者GM谱的时间稳定性,并定义疾病和进展的多变量模型。

方法

我们在0、6和12个月时评估了74例PD患者和74例家庭对照(HC)的经过验证的临床问卷和粪便样本。根据左旋多巴等效剂量和运动严重程度指标定义疾病进展的快慢。19例开始接受深部脑刺激或左旋多巴-卡比多巴肠凝胶治疗的PD患者在治疗开始后的0、6和12个月分别进行评估。

结果

相对于对照组,PD患者中产生短链脂肪酸的细菌(如 、 和 )持续存在代表性不足的情况。未观察到开始DAT对GM与PD相关性的持续影响。PD进展分析表明,在疾病进展较快的PD患者中, 属在0个月和12个月时代表性不足。在扩增子序列变异分类分辨率下进行评估时,整合微生物群丰度和营养状况的两阶段预测模型提高了预测能力(曲线下面积从0.58变为0.64)。

结论

我们展示了对PD患者的纵向GM研究,结果显示GM谱持续改变,提示产丁酸潜力降低。DAT在短期和长期内对GM产生了不同的影响。我们发现特定的GM谱与饮食因素相结合可改善对PD患者疾病进展的预测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ccb7/9152137/80ae3632a87d/fnagi-14-875261-g001.jpg

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