使用肠道微生物群作为结直肠癌的诊断工具:机器学习技术揭示了有希望的结果。

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS
Fang Lu, Ting Lei, Jie Zhou, Hao Liang, Ping Cui, Taiping Zuo, Li Ye, Hui Chen, Jiegang Huang
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引用次数: 0

摘要

介绍。越来越多的证据表明肠道微生物群与结直肠癌(CRC)之间存在相关性。假设/差距语句。然而,很少有研究将肠道微生物群作为诊断crc的生物标志物。本研究的目的是探讨基于肠道微生物群的机器学习(ML)模型是否可以用于诊断CRC并识别模型中的关键生物标志物。我们对38名参与者的粪便样本进行了16S rRNA基因测序,其中包括17名健康受试者和21名结直肠癌患者。采用8种基于粪便微生物群操作分类单位(OTUs)的监督ML算法诊断CRC,并对模型的识别、校准和临床实用性进行了评估。最后,使用随机森林(RF)算法确定了关键的肠道微生物群。我们发现结直肠癌与肠道菌群失调有关。通过对有监督机器学习算法的综合评估,我们发现不同算法在使用粪便微生物组的预测性能上存在显著差异。不同的数据筛选方法对预测模型的优化起着重要的作用。我们发现naïve贝叶斯算法[NB,准确率=0.917,曲线下面积(AUC)=0.926]、RF(准确率=0.750,AUC=0.926)和logistic回归(LR,准确率=0.750,AUC=0.889)对CRC具有较高的预测潜力。此外,模型中的重要特征s__metagenome_g__Lachnospiraceae_ND3007_group (AUC=0.814)、s__Escherichia_coli_g__Escherichia-Shigella (AUC=0.784)和s__unclassified_g__Prevotella (AUC=0.750)均可作为crc的诊断性生物标志物。我们的研究结果表明肠道菌群失调与结直肠癌之间存在关联,并证明了肠道菌群诊断癌症的可行性。细菌s_ metagenome_g_ lachnospiraceae_nd3007_group、s_ escherichia _coli_g_ escherichia - shigella和s_ unclassified_g_ prevotella是结直肠癌的关键生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Using gut microbiota as a diagnostic tool for colorectal cancer: machine learning techniques reveal promising results.

Introduction. Increasing evidence suggests a correlation between gut microbiota and colorectal cancer (CRC).Hypothesis/Gap Statement. However, few studies have used gut microbiota as a diagnostic biomarker for CRC.Aim. The objective of this study was to explore whether a machine learning (ML) model based on gut microbiota could be used to diagnose CRC and identify key biomarkers in the model.Methodology. We sequenced the 16S rRNA gene from faecal samples of 38 participants, including 17 healthy subjects and 21 CRC patients. Eight supervised ML algorithms were used to diagnose CRC based on faecal microbiota operational taxonomic units (OTUs), and the models were evaluated in terms of identification, calibration and clinical practicality for optimal modelling parameters. Finally, the key gut microbiota was identified using the random forest (RF) algorithm.Results. We found that CRC was associated with the dysregulation of gut microbiota. Through a comprehensive evaluation of supervised ML algorithms, we found that different algorithms had significantly different prediction performance using faecal microbiomes. Different data screening methods played an important role in optimization of the prediction models. We found that naïve Bayes algorithms [NB, accuracy=0.917, area under the curve (AUC)=0.926], RF (accuracy=0.750, AUC=0.926) and logistic regression (LR, accuracy=0.750, AUC=0.889) had high predictive potential for CRC. Furthermore, important features in the model, namely s__metagenome_g__Lachnospiraceae_ND3007_group (AUC=0.814), s__Escherichia_coli_g__Escherichia-Shigella (AUC=0.784) and s__unclassified_g__Prevotella (AUC=0.750), could each be used as diagnostic biomarkers of CRC.Conclusions. Our results suggested an association between gut microbiota dysregulation and CRC, and demonstrated the feasibility of the gut microbiota to diagnose cancer. The bacteria s__metagenome_g__Lachnospiraceae_ND3007_group, s__Escherichia_coli_g__Escherichia-Shigella and s__unclassified_g__Prevotella were key biomarkers for CRC.

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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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