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缺血性中风的发生及预后与编码色氨酸代谢酶的基因变异之间的关系。

Relationships of Ischemic Stroke Occurrence and Outcome with Gene Variants Encoding Enzymes of Tryptophan Metabolism.

作者信息

Boros Fanni Annamária, Maszlag-Török Rita, Szűcs Mónika, Annus Ádám, Klivényi Péter, Vécsei László

机构信息

Department of Neurology, Faculty of Medicine, Albert Szent-Györgyi Clinical Center, University of Szeged, H-6725 Szeged, Hungary.

Department of Medical Physics and Informatics, Faculty of Science and Informatics, Albert Szent-Györgyi Medical School, University of Szeged, H-6720 Szeged, Hungary.

出版信息

Biomedicines. 2021 Oct 11;9(10):1441. doi: 10.3390/biomedicines9101441.

Abstract

Ischemic stroke is among the leading causes of mortality and long-term disability worldwide. Among stroke risk factors the importance of genetic background is gaining interest. There is a growing body of evidence of changes of metabolite levels and enzyme activities involved in the conversion of Trp during the course of cerebral ischemia. We compared the frequencies of ten SNPs of five genes related to Trp metabolism between groups of 122 ischemic stroke patients and 120 control individuals. Furthermore, we examined the mRNA levels of , and genes in peripheral venous blood with the aim of assessing (i) whether there are changes in their expression during the course of stroke and (ii) does any of their investigated SNPs have an impact on gene expression. In seven cases out of ten studied polymorphisms we detected significant differences in frequencies in relation to ischemic stroke occurrence, etiology, and clinical parameters. We also detected changes in the expression of and genes during the course of the disease. We found that those IDO1 variants which show a trend towards elevated mRNA level are more frequent in stroke patients than in controls. Our results are important novel observations which suggest a causal relationship between elevated expression and stroke etiology.

摘要

缺血性中风是全球范围内导致死亡和长期残疾的主要原因之一。在中风风险因素中,遗传背景的重要性日益受到关注。越来越多的证据表明,在脑缺血过程中,色氨酸转化过程中涉及的代谢物水平和酶活性发生了变化。我们比较了122例缺血性中风患者和120例对照个体之间与色氨酸代谢相关的五个基因的十个单核苷酸多态性(SNP)的频率。此外,我们检测了外周静脉血中、和基因的mRNA水平,目的是评估:(i)中风过程中它们的表达是否有变化;(ii)所研究的任何一个SNP是否对基因表达有影响。在十个研究的多态性中,有七个我们检测到与缺血性中风的发生、病因和临床参数相关的频率存在显著差异。我们还在疾病过程中检测到和基因表达的变化。我们发现,那些mRNA水平有升高趋势的吲哚胺2,3-双加氧酶1(IDO1)变体在中风患者中比在对照中更常见。我们的结果是重要的新发现,表明IDO1表达升高与中风病因之间存在因果关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d177/8533114/153a1d9816ad/biomedicines-09-01441-g002.jpg

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