4.7 Article

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

期刊

BIOMEDICINES
卷 9, 期 10, 页码 -

出版社

MDPI
DOI: 10.3390/biomedicines9101441

关键词

gene expression; genotyping; IDO1; ischemic stroke; KYAT1; kynurenine pathway; SNP; stroke etiology; Trp metabolism; TPH1

资金

  1. Economic Development and Innovation Operational Programme [GINOP-2.3.2-15-2016-00048, GINOP-2.3.2-15-2016-00034, TUDFO 47138-1/2019-ITM, OTKA-138125-K]
  2. University of Szeged [5499]
  3. New National Excellence Program of the Ministry for Innovation and Technology from the source of the National Research, Development and Innovation Fund [UNKP-20-4]

向作者/读者索取更多资源

This study highlights the importance of genetic background in the occurrence, etiology, and clinical parameters of ischemic stroke. Significant differences in frequencies related to ischemic stroke were detected in seven out of ten studied polymorphisms. Changes in expression levels of IDO1 and TPH1 genes during the disease course suggest a potential causal relationship with stroke etiology.
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 TPH1, IDO1 and KYAT1 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 TPH1 and IDO1 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 IDO1 expression and stroke etiology.

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