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分析一对表现型不同的进行性核上性麻痹双胞胎的遗传和 MRI 变化、血液标志物和危险因素。

Analysis of Genetic and MRI Changes, Blood Markers, and Risk Factors in a Twin Pair Discordant of Progressive Supranuclear Palsy.

机构信息

Medical Imaging Centre, Semmelweis University, 1082 Budapest, Hungary.

Neurology Department, Medical Centre Hungarian Defence Forces, 1134 Budapest, Hungary.

出版信息

Medicina (Kaunas). 2023 Sep 22;59(10):1696. doi: 10.3390/medicina59101696.

DOI:10.3390/medicina59101696
PMID:37893413
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10608279/
Abstract

: Progressive supranuclear palsy (PSP) is a neurodegenerative disease, a tauopathy, which results in a wide clinical spectrum of neurological symptoms. The diagnosis is mostly based on clinical signs and neuroimaging; however, possible biomarkers for screening have been under investigation, and the role of the gut microbiome is unknown. The aim of our study was to identify potential blood biomarkers and observe variations in the gut microbiome within a PSP discordant monozygotic twin pair. : Anthropometric measurements, neuropsychological tests, and the neurological state were evaluated. Blood was collected for metabolic profiling and for the detection of neurodegenerative and vascular biomarkers. Both the gut microbiome and brain MRI results were thoroughly examined. : We found a relevant difference between alpha-synuclein levels and moderate difference in the levels of MMP-2, MB, Apo-A1, Apo-CIII, and Apo-H. With respect to the ratios, a small difference was observed for ApoA1/SAA and ApoB/ApoA1. Using a microbiome analysis, we also discovered a relative dysbiosis, and the MRI results revealed midbrain and frontoparietal cortical atrophy along with a reduction in overall brain volumes and an increase in white matter lesions in the affected twin. : We observed significant differences between the unaffected and affected twins in some risk factors and blood biomarkers, along with disparities in the gut microbiome. Additionally, we detected abnormalities in brain MRI results and alterations in cognitive functions.

摘要

进行性核上性麻痹(PSP)是一种神经退行性疾病,是一种tau 病,导致广泛的神经症状谱。诊断主要基于临床体征和神经影像学;然而,一直在研究可能用于筛查的生物标志物,肠道微生物组的作用尚不清楚。我们的研究目的是确定潜在的血液生物标志物,并观察 PSP 不一致的同卵双胞胎中肠道微生物组的变化。

对人体测量学测量、神经心理学测试和神经状态进行了评估。采集血液进行代谢谱分析和检测神经退行性和血管生物标志物。对肠道微生物组和脑 MRI 结果进行了全面检查。

我们发现 alpha-synuclein 水平存在显著差异,MMP-2、MB、Apo-A1、Apo-CIII 和 Apo-H 水平存在中度差异。就比值而言,ApoA1/SAA 和 ApoB/ApoA1 观察到微小差异。通过微生物组分析,我们还发现了相对的菌群失调,MRI 结果显示中脑和额顶皮质萎缩,以及受影响双胞胎的总脑体积减少和白质病变增加。

我们观察到在一些风险因素和血液生物标志物方面,未受影响的双胞胎和受影响的双胞胎之间存在显著差异,以及肠道微生物组的差异。此外,我们还发现脑 MRI 结果异常和认知功能改变。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7668/10608279/e65e68d7b09f/medicina-59-01696-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7668/10608279/27daf493c00d/medicina-59-01696-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7668/10608279/9d37debff12a/medicina-59-01696-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7668/10608279/dbd91790b3aa/medicina-59-01696-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7668/10608279/98386418de0d/medicina-59-01696-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7668/10608279/d088c51951b2/medicina-59-01696-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7668/10608279/e65e68d7b09f/medicina-59-01696-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7668/10608279/27daf493c00d/medicina-59-01696-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7668/10608279/9d37debff12a/medicina-59-01696-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7668/10608279/dbd91790b3aa/medicina-59-01696-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7668/10608279/98386418de0d/medicina-59-01696-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7668/10608279/d088c51951b2/medicina-59-01696-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7668/10608279/e65e68d7b09f/medicina-59-01696-g006.jpg

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