Using artificial intelligence and promoter-level transcriptome analysis to identify a biomarker as a possible prognostic predictor of cardiac complications in male patients with Fabry disease

IF 1.8 4区 医学 Q3 GENETICS & HEREDITY
Hiroshi Kobayashi , Norio Nakata , Sayoko Izuka , Kenichi Hongo , Masako Nishikawa
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Abstract

Fabry disease is the most frequently occurring form of lysosomal disease in Japan, and is characterized by a wide variety of conditions. Primarily, the three major types of concerns associated with Fabry disease observed during adulthood that must be prevented are central nervous system, renal, and cardiac complications. Cardiac complications, such as cardiomyopathy, cardiac muscle fibrosis, and severe arrhythmia, are the most common mortality causes in patients with Fabry disease. To predict cardiac complications of Fabry disease, we extracted RNA from the venous blood of patients for cap analysis of gene expression (CAGE), performed likelihood ratio tests for each RNA expression dataset obtained from individuals with and without cardiac complications, and analyzed the correlation between cardiac functional factors observed using magnetic resonance imaging data extracted using artificial intelligence algorithms and RNA expression. Our findings showed that CHN1 expression was significantly higher in male Fabry disease patients with cardiac complications and that it could be associated with many cardiac functional factors. CHN1 encodes a GTPase-activating protein, chimerin 1, which is specific to the GTP-binding protein Rac (involved in oxidative stress generation and the promotion of myocardial fibrosis). Thus, CHN1 is a potential predictive biomarker of cardiac complications in Fabry disease; however, further studies are required to confirm this observation.
利用人工智能和启动子级转录组分析确定一种生物标记物,作为法布里病男性患者心脏并发症的可能预后预测因子
法布里病是日本最常见的溶酶体疾病,表现为多种病症。法布里病在成年期主要有三种必须预防的并发症,即中枢神经系统并发症、肾脏并发症和心脏并发症。心脏并发症,如心肌病、心肌纤维化和严重心律失常,是法布里病患者最常见的死亡原因。为了预测法布里病的心脏并发症,我们提取了患者静脉血中的 RNA 进行基因表达上限分析(CAGE),对从有心脏并发症和无心脏并发症的个体中获得的每个 RNA 表达数据集进行似然比检验,并分析了利用人工智能算法提取的磁共振成像数据观察到的心脏功能因素与 RNA 表达之间的相关性。我们的研究结果表明,在有心脏并发症的男性法布里病患者中,CHN1的表达量明显较高,而且它可能与许多心脏功能因素有关。CHN1 编码一种 GTP 酶激活蛋白--嵌合蛋白 1,它对 GTP 结合蛋白 Rac(参与氧化应激的产生和心肌纤维化的促进)具有特异性。因此,CHN1 是法布里病心脏并发症的潜在预测性生物标志物;然而,要证实这一观察结果还需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports Biochemistry, Genetics and Molecular Biology-Endocrinology
CiteScore
4.00
自引率
5.30%
发文量
105
审稿时长
33 days
期刊介绍: Molecular Genetics and Metabolism Reports is an open access journal that publishes molecular and metabolic reports describing investigations that use the tools of biochemistry and molecular biology for studies of normal and diseased states. In addition to original research articles, sequence reports, brief communication reports and letters to the editor are considered.
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