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肠脑微生物组在肌张力障碍患者中的组成。

Gut Microbiome Composition in Dystonia Patients.

机构信息

Department of Neurology, University Medical Center Groningen, University of Groningen, 9700RB Groningen, The Netherlands.

Expertise Center Movement Disorders Groningen, University Medical Center Groningen, 9700RB Groningen, The Netherlands.

出版信息

Int J Mol Sci. 2023 Jan 25;24(3):2383. doi: 10.3390/ijms24032383.

DOI:10.3390/ijms24032383
PMID:36768705
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9916458/
Abstract

Dystonia is a movement disorder in which patients have involuntary abnormal movements or postures. Non-motor symptoms, such as psychiatric symptoms, sleep problems and fatigue, are common. We hypothesise that the gut microbiome might play a role in the pathophysiology of the (non-)motor symptoms in dystonia via the gut-brain axis. This exploratory study investigates the composition of the gut microbiome in dystonia patients compared to healthy controls. Furthermore, the abundance of neuro-active metabolic pathways, which might be implicated in the (non-)motor symptoms, was investigated. We performed both metagenomic and 16S rRNA sequencing on the stool samples of three subtypes of dystonia (27 cervical dystonia, 20 dopa-responsive dystonia and 24 myoclonus-dystonia patients) and 25 controls. While microbiome alpha and beta diversity was not different between dystonia patients and controls, dystonia patients had higher abundances of and , and a lower abundance of compared to controls. For those with dystonia, non-motor symptoms and the levels of neurotransmitters in plasma explained the variance in the gut microbiome composition. Several neuro-active metabolic pathways, especially tryptophan degradation, were less abundant in the dystonia patients compared to controls. This suggest that the gut-brain axis might be involved in the pathophysiology of dystonia. Further studies are necessary to confirm our preliminary findings.

摘要

肌张力障碍是一种运动障碍,患者会出现不自主的异常运动或姿势。非运动症状(如精神症状、睡眠问题和疲劳)很常见。我们假设肠道微生物组可能通过肠脑轴在肌张力障碍的(非)运动症状的病理生理学中发挥作用。这项探索性研究比较了肌张力障碍患者和健康对照者的肠道微生物组组成。此外,还研究了可能与(非)运动症状有关的神经活性代谢途径的丰度。我们对三种亚型的肌张力障碍(27 例颈肌张力障碍、20 例多巴反应性肌张力障碍和 24 例肌阵挛性肌张力障碍患者)和 25 名对照者的粪便样本进行了宏基因组和 16S rRNA 测序。虽然肌张力障碍患者和对照组之间的微生物组α多样性和β多样性没有差异,但与对照组相比,肌张力障碍患者的 和 丰度更高,而 丰度更低。对于那些有肌张力障碍的患者,非运动症状和血浆中神经递质的水平解释了肠道微生物组组成的差异。一些神经活性代谢途径,特别是色氨酸降解,在肌张力障碍患者中比对照组更为缺乏。这表明肠脑轴可能参与了肌张力障碍的病理生理学。需要进一步的研究来证实我们的初步发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f5e/9916458/2f4232fa1375/ijms-24-02383-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f5e/9916458/570b227908d6/ijms-24-02383-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f5e/9916458/e8c5c6955c72/ijms-24-02383-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f5e/9916458/f82228f5e7c1/ijms-24-02383-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f5e/9916458/2f4232fa1375/ijms-24-02383-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f5e/9916458/570b227908d6/ijms-24-02383-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f5e/9916458/e8c5c6955c72/ijms-24-02383-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f5e/9916458/f82228f5e7c1/ijms-24-02383-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f5e/9916458/2f4232fa1375/ijms-24-02383-g004.jpg

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