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本文引用的文献

1
Meta-Analysis of Dilated Cardiomyopathy Using Cardiac RNA-Seq Transcriptomic Datasets.基于心脏 RNA-Seq 转录组数据集的扩张型心肌病的荟萃分析
Genes (Basel). 2020 Jan 4;11(1):60. doi: 10.3390/genes11010060.
2
Machine Learning Classifiers for Endometriosis Using Transcriptomics and Methylomics Data.利用转录组学和甲基组学数据的子宫内膜异位症机器学习分类器
Front Genet. 2019 Sep 4;10:766. doi: 10.3389/fgene.2019.00766. eCollection 2019.
3
Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype.基于图的基因组比对和基因分型与 HISAT2 和 HISAT-genotype。
Nat Biotechnol. 2019 Aug;37(8):907-915. doi: 10.1038/s41587-019-0201-4. Epub 2019 Aug 2.
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Mitochondrial genome variations in idiopathic dilated cardiomyopathy.特发性扩张型心肌病中线粒体基因组的变异。
Mitochondrion. 2019 Sep;48:51-59. doi: 10.1016/j.mito.2019.03.003. Epub 2019 Mar 22.
5
Platform-independent approach for cancer detection from gene expression profiles of peripheral blood cells.从外周血细胞的基因表达谱中进行癌症检测的平台独立方法。
Brief Bioinform. 2020 May 21;21(3):1006-1015. doi: 10.1093/bib/bbz027.
6
Genome-wide DNA methylation encodes cardiac transcriptional reprogramming in human ischemic heart failure.全基因组 DNA 甲基化在人类缺血性心力衰竭中编码心脏转录重编程。
Lab Invest. 2019 Mar;99(3):371-386. doi: 10.1038/s41374-018-0104-x. Epub 2018 Aug 8.
7
Identification of usual interstitial pneumonia pattern using RNA-Seq and machine learning: challenges and solutions.使用 RNA-Seq 和机器学习识别常见间质性肺炎模式:挑战与解决方案。
BMC Genomics. 2018 May 9;19(Suppl 2):101. doi: 10.1186/s12864-018-4467-6.
8
Bioinformatics method identifies potential biomarkers of dilated cardiomyopathy in a human induced pluripotent stem cell-derived cardiomyocyte model.生物信息学方法在人诱导多能干细胞衍生的心肌细胞模型中鉴定扩张型心肌病的潜在生物标志物。
Exp Ther Med. 2017 Oct;14(4):2771-2778. doi: 10.3892/etm.2017.4850. Epub 2017 Jul 28.
9
Dilated Cardiomyopathy: Genetic Determinants and Mechanisms.扩张型心肌病:遗传决定因素与机制
Circ Res. 2017 Sep 15;121(7):731-748. doi: 10.1161/CIRCRESAHA.116.309396.
10
Artificial Intelligence in Precision Cardiovascular Medicine.人工智能在精准心血管医学中的应用。
J Am Coll Cardiol. 2017 May 30;69(21):2657-2664. doi: 10.1016/j.jacc.2017.03.571.

基于机器学习的临床心肌病分类和诊断。

Machine learning-based classification and diagnosis of clinical cardiomyopathies.

机构信息

Bioinformatics & Artificial Intelligence Laboratory, Center for Hypertension and Precision Medicine, Program in Physiological Genomics, Department of Physiology and Pharmacology, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.

Bioinformatics Program, University of Toledo College of Medicine and Life Sciences, Toledo, Ohio.

出版信息

Physiol Genomics. 2020 Sep 1;52(9):391-400. doi: 10.1152/physiolgenomics.00063.2020. Epub 2020 Aug 3.

DOI:10.1152/physiolgenomics.00063.2020
PMID:32744882
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7509247/
Abstract

Dilated cardiomyopathy (DCM) and ischemic cardiomyopathy (ICM) are two common types of cardiomyopathies leading to heart failure. Accurate diagnostic classification of different types of cardiomyopathies is critical for precision medicine in clinical practice. In this study, we hypothesized that machine learning (ML) can be used as a novel diagnostic approach to analyze cardiac transcriptomic data for classifying clinical cardiomyopathies. RNA-Seq data of human left ventricle tissues were collected from 41 DCM patients, 47 ICM patients, and 49 nonfailure controls (NF) and tested using five ML algorithms: support vector machine with radial kernel (svmRadial), neural networks with principal component analysis (pcaNNet), decision tree (DT), elastic net (ENet), and random forest (RF). Initial ML classifications achieved ~93% accuracy (svmRadial) for NF vs. DCM, ~82% accuracy (RF) for NF vs. ICM, and ~80% accuracy (ENet and svmRadial) for DCM vs. ICM. Next, 50 highly contributing genes (HCGs) for classifying NF and DCM, 68 HCGs for classifying NF and ICM, and 59 HCGs for classifying DCM and ICM were selected for retraining ML models. Impressively, the retrained models achieved ~90% accuracy (RF) for NF vs. DCM, ~90% accuracy (pcaNNet) for NF vs. ICM, and ~85% accuracy (pcaNNet and RF) for DCM vs. ICM. Pathway analyses further confirmed the involvement of those selected HCGs in cardiac dysfunctions such as cardiomyopathies, cardiac hypertrophies, and fibrosis. Overall, our study demonstrates the promising potential of using artificial intelligence via ML modeling as a novel approach to achieve a greater level of precision in diagnosing different types of cardiomyopathies.

摘要

扩张型心肌病(DCM)和缺血性心肌病(ICM)是导致心力衰竭的两种常见心肌病类型。准确诊断不同类型的心肌病对于临床实践中的精准医学至关重要。在这项研究中,我们假设机器学习(ML)可以作为一种新的诊断方法,用于分析心脏转录组数据以对临床心肌病进行分类。从 41 名 DCM 患者、47 名 ICM 患者和 49 名非衰竭对照(NF)的人类左心室组织中收集了 RNA-Seq 数据,并使用 5 种 ML 算法进行了测试:具有径向核的支持向量机(svmRadial)、基于主成分分析的神经网络(pcaNNet)、决策树(DT)、弹性网络(ENet)和随机森林(RF)。初始 ML 分类对 NF 与 DCM 的准确率约为 93%(svmRadial),对 NF 与 ICM 的准确率约为 82%(RF),对 DCM 与 ICM 的准确率约为 80%(ENet 和 svmRadial)。接下来,选择了 50 个对 NF 和 DCM 分类有重要贡献的基因(HCGs)、68 个对 NF 和 ICM 分类有重要贡献的 HCGs 和 59 个对 DCM 和 ICM 分类有重要贡献的 HCGs 用于重新训练 ML 模型。令人印象深刻的是,重新训练的模型对 NF 与 DCM 的准确率约为 90%(RF),对 NF 与 ICM 的准确率约为 90%(pcaNNet),对 DCM 与 ICM 的准确率约为 85%(pcaNNet 和 RF)。通路分析进一步证实了这些选定的 HCGs 参与了心脏功能障碍,如心肌病、心脏肥大和纤维化。总体而言,我们的研究表明,通过 ML 建模使用人工智能具有很大的潜力,可以实现对不同类型心肌病进行更高水平的精确诊断。