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特发性快速眼动睡眠行为障碍(iRBD)与多系统萎缩(MSA)和帕金森病(PD)具有相似的粪便短链脂肪酸改变。

Idiopathic Rapid Eye Movement Sleep Behavior Disorder (iRBD) Shares Similar Fecal Short-Chain Fatty Acid Alterations with Multiple System Atrophy (MSA) and Parkinson's Disease (PD).

机构信息

Department of Neurology and Institute of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Laboratory for Translational Research of Neurodegenerative Diseases, Shanghai Institute for Advanced Immunochemical Studies (SIAIS), Shanghai Tech University, Shanghai, China.

出版信息

Mov Disord. 2024 Aug;39(8):1397-1402. doi: 10.1002/mds.29803. Epub 2024 Apr 1.


DOI:10.1002/mds.29803
PMID:38561921
Abstract

BACKGROUND: Idiopathic rapid eye movement sleep behavior disorder (iRBD) is considered as a prodromal stage of synucleinopathies. Fecal short-chain fatty acid (SCFA) changes in iRBD and the relationships with synucleinopathies have never been investigated. OBJECTIVES: To investigate fecal SCFA changes among iRBD, multiple system atrophy (MSA), and Parkinson's disease (PD), and evaluate their relationships. METHODS: Fecal SCFAs and gut microbiota were measured in 29 iRBD, 42 MSA, 40 PD, and 35 normal controls (NC) using gas chromatography-mass spectrometry and 16S rRNA gene sequencing. RESULTS: Compared with NC, fecal SCFA levels (propionic, acetic, and butyric acid) were lower in iRBD, MSA, and PD. Combinations of these SCFAs could differentiate NC from iRBD (AUC 0.809), MSA (AUC 0.794), and PD (AUC 0.701). Decreased fecal SCFAs were associated with the common reducing SCFA-producing gut microbiota in iRBD, MSA, and PD. CONCLUSIONS: iRBD shares similar fecal SCFA alterations with MSA and PD, and the combination of these SCFAs might be a potential synucleinopathies-related biomarker. © 2024 International Parkinson and Movement Disorder Society.

摘要

背景:特发性快速眼动睡眠行为障碍(iRBD)被认为是突触核蛋白病的前驱阶段。iRBD 粪便短链脂肪酸(SCFA)的变化及其与突触核蛋白病的关系尚未被研究过。 目的:调查 iRBD、多系统萎缩(MSA)和帕金森病(PD)患者粪便 SCFA 的变化,并评估它们之间的关系。 方法:采用气相色谱-质谱法和 16S rRNA 基因测序法,对 29 例 iRBD、42 例 MSA、40 例 PD 和 35 例正常对照(NC)患者的粪便 SCFA 和肠道微生物群进行了测量。 结果:与 NC 相比,iRBD、MSA 和 PD 患者粪便 SCFA 水平(丙酸、乙酸和丁酸)较低。这些 SCFA 的组合可以区分 NC 与 iRBD(AUC 0.809)、MSA(AUC 0.794)和 PD(AUC 0.701)。粪便 SCFA 的减少与 iRBD、MSA 和 PD 中常见的减少 SCFA 产生的肠道微生物群有关。 结论:iRBD 与 MSA 和 PD 具有相似的粪便 SCFA 改变,这些 SCFA 的组合可能是一种潜在的突触核蛋白病相关生物标志物。

相似文献

[1]
Idiopathic Rapid Eye Movement Sleep Behavior Disorder (iRBD) Shares Similar Fecal Short-Chain Fatty Acid Alterations with Multiple System Atrophy (MSA) and Parkinson's Disease (PD).

Mov Disord. 2024-8

[2]
Short-Chain Fatty Acid-Producing Gut Microbiota Is Decreased in Parkinson's Disease but Not in Rapid-Eye-Movement Sleep Behavior Disorder.

mSystems. 2020-12-8

[3]
Association of Fecal and Plasma Levels of Short-Chain Fatty Acids With Gut Microbiota and Clinical Severity in Patients With Parkinson Disease.

Neurology. 2022-2-22

[4]
Transcranial sonography in idiopathic REM sleep behavior disorder and multiple system atrophy.

Psychiatry Clin Neurosci. 2017-1-9

[5]
Parkinson's Disease Is Associated with Impaired Gut-Blood Barrier for Short-Chain Fatty Acids.

Mov Disord. 2022-8

[6]
Plasma Short-Chain Fatty Acids Differences in Multiple System Atrophy from Parkinson's Disease.

J Parkinsons Dis. 2021

[7]
Detection of α-Synuclein in Oral Mucosa by Seed Amplification Assay in Synucleinopathies and Isolated REM Sleep Behavior Disorder.

Mov Disord. 2024-8

[8]
Sensorimotor gating deficits in multiple system atrophy: comparison with Parkinson's disease and idiopathic REM sleep behavior disorder.

Parkinsonism Relat Disord. 2014-3

[9]
Relationships of gut microbiota, short-chain fatty acids, inflammation, and the gut barrier in Parkinson's disease.

Mol Neurodegener. 2021-2-8

[10]
Short chain fatty acids and gut microbiota differ between patients with Parkinson's disease and age-matched controls.

Parkinsonism Relat Disord. 2016-11

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