• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

一种融合功能磁共振成像(fMRI)和基因数据的混合机器学习方法:两者结合可改善精神分裂症的分类。

A Hybrid Machine Learning Method for Fusing fMRI and Genetic Data: Combining both Improves Classification of Schizophrenia.

作者信息

Yang Honghui, Liu Jingyu, Sui Jing, Pearlson Godfrey, Calhoun Vince D

机构信息

Department of Environment Engineering, Northwestern Polytechnical University Xi'an, China.

出版信息

Front Hum Neurosci. 2010 Oct 25;4:192. doi: 10.3389/fnhum.2010.00192. eCollection 2010.

DOI:10.3389/fnhum.2010.00192
PMID:21119772
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2990459/
Abstract

We demonstrate a hybrid machine learning method to classify schizophrenia patients and healthy controls, using functional magnetic resonance imaging (fMRI) and single nucleotide polymorphism (SNP) data. The method consists of four stages: (1) SNPs with the most discriminating information between the healthy controls and schizophrenia patients are selected to construct a support vector machine ensemble (SNP-SVME). (2) Voxels in the fMRI map contributing to classification are selected to build another SVME (Voxel-SVME). (3) Components of fMRI activation obtained with independent component analysis (ICA) are used to construct a single SVM classifier (ICA-SVMC). (4) The above three models are combined into a single module using a majority voting approach to make a final decision (Combined SNP-fMRI). The method was evaluated by a fully validated leave-one-out method using 40 subjects (20 patients and 20 controls). The classification accuracy was: 0.74 for SNP-SVME, 0.82 for Voxel-SVME, 0.83 for ICA-SVMC, and 0.87 for Combined SNP-fMRI. Experimental results show that better classification accuracy was achieved by combining genetic and fMRI data than using either alone, indicating that genetic and brain function representing different, but partially complementary aspects, of schizophrenia etiopathology. This study suggests an effective way to reassess biological classification of individuals with schizophrenia, which is also potentially useful for identifying diagnostically important markers for the disorder.

摘要

我们展示了一种混合机器学习方法,用于使用功能磁共振成像(fMRI)和单核苷酸多态性(SNP)数据对精神分裂症患者和健康对照进行分类。该方法包括四个阶段:(1)选择在健康对照和精神分裂症患者之间具有最具区分性信息的SNP,以构建支持向量机集成(SNP-SVME)。(2)选择fMRI图谱中有助于分类的体素,以构建另一个SVME(体素-SVME)。(3)使用独立成分分析(ICA)获得的fMRI激活成分来构建单个支持向量机分类器(ICA-SVMC)。(4)使用多数投票方法将上述三个模型组合成一个单一模块以做出最终决策(联合SNP-fMRI)。该方法通过使用40名受试者(20名患者和20名对照)的完全验证的留一法进行评估。分类准确率为:SNP-SVME为0.74,体素-SVME为0.82,ICA-SVMC为0.83,联合SNP-fMRI为0.87。实验结果表明,将遗传数据和fMRI数据结合起来比单独使用任何一种数据都能获得更好的分类准确率,这表明遗传和脑功能代表了精神分裂症病因学中不同但部分互补的方面。这项研究提出了一种重新评估精神分裂症个体生物学分类的有效方法,这对于识别该疾病的诊断重要标志物也可能是有用的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8eb/2990459/7be9623cc337/fnhum-04-00192-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8eb/2990459/574369e072e0/fnhum-04-00192-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8eb/2990459/bff6027d6d10/fnhum-04-00192-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8eb/2990459/7be9623cc337/fnhum-04-00192-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8eb/2990459/574369e072e0/fnhum-04-00192-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8eb/2990459/bff6027d6d10/fnhum-04-00192-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8eb/2990459/7be9623cc337/fnhum-04-00192-g003.jpg

相似文献

1
A Hybrid Machine Learning Method for Fusing fMRI and Genetic Data: Combining both Improves Classification of Schizophrenia.一种融合功能磁共振成像(fMRI)和基因数据的混合机器学习方法:两者结合可改善精神分裂症的分类。
Front Hum Neurosci. 2010 Oct 25;4:192. doi: 10.3389/fnhum.2010.00192. eCollection 2010.
2
Integrating fMRI and SNP data for biomarker identification for schizophrenia with a sparse representation based variable selection method.基于稀疏表示变量选择方法的 fMRI 和 SNP 数据整合,用于精神分裂症的生物标志物识别。
BMC Med Genomics. 2013;6 Suppl 3(Suppl 3):S2. doi: 10.1186/1755-8794-6-S3-S2. Epub 2013 Nov 11.
3
A novel fuzzy rough selection of non-linearly extracted features for schizophrenia diagnosis using fMRI.一种使用 fMRI 进行精神分裂症诊断的非线性提取特征的新型模糊粗糙选择方法。
Comput Methods Programs Biomed. 2018 Mar;155:139-152. doi: 10.1016/j.cmpb.2017.12.001. Epub 2017 Dec 6.
4
fMRI volume classification using a 3D convolutional neural network robust to shifted and scaled neuronal activations.使用对移位和缩放神经元激活具有鲁棒性的 3D 卷积神经网络进行 fMRI 体积分类。
Neuroimage. 2020 Dec;223:117328. doi: 10.1016/j.neuroimage.2020.117328. Epub 2020 Sep 5.
5
Combining fMRI and SNP data to investigate connections between brain function and genetics using parallel ICA.结合功能磁共振成像(fMRI)和单核苷酸多态性(SNP)数据,使用并行独立成分分析(ICA)研究脑功能与遗传学之间的联系。
Hum Brain Mapp. 2009 Jan;30(1):241-55. doi: 10.1002/hbm.20508.
6
Group ICA for identifying biomarkers in schizophrenia: 'Adaptive' networks via spatially constrained ICA show more sensitivity to group differences than spatio-temporal regression.组独立成分分析在精神分裂症生物标志物识别中的应用:通过空间约束独立成分分析的“适应性”网络比时空回归更能显示出对组间差异的敏感性。
Neuroimage Clin. 2019;22:101747. doi: 10.1016/j.nicl.2019.101747. Epub 2019 Mar 5.
7
Dimensionality of ICA in resting-state fMRI investigated by feature optimized classification of independent components with SVM.通过支持向量机对独立成分进行特征优化分类来研究静息态功能磁共振成像中独立成分分析的维度。
Front Hum Neurosci. 2015 May 8;9:259. doi: 10.3389/fnhum.2015.00259. eCollection 2015.
8
[Single-modal neuroimaging computer aided diagnosis for schizophrenia based on ensemble learning using privileged information].基于使用特权信息的集成学习的精神分裂症单模态神经影像学计算机辅助诊断
Sheng Wu Yi Xue Gong Cheng Xue Za Zhi. 2020 Jun 25;37(3):405-411. doi: 10.7507/1001-5515.201905029.
9
Brain MRI-based 3D Convolutional Neural Networks for Classification of Schizophrenia and Controls.基于脑部磁共振成像的三维卷积神经网络用于精神分裂症与对照的分类
Annu Int Conf IEEE Eng Med Biol Soc. 2020 Jul;2020:1742-1745. doi: 10.1109/EMBC44109.2020.9176610.
10
Combination of FMRI-SMRI-EEG data improves discrimination of schizophrenia patients by ensemble feature selection.功能磁共振成像-结构性磁共振成像-脑电图数据的组合通过集成特征选择提高了对精神分裂症患者的辨别能力。
Annu Int Conf IEEE Eng Med Biol Soc. 2014;2014:3889-92. doi: 10.1109/EMBC.2014.6944473.

引用本文的文献

1
Schizophrenia Detection and Classification: A Systematic Review of the Last Decade.精神分裂症的检测与分类:过去十年的系统综述
Diagnostics (Basel). 2024 Nov 29;14(23):2698. doi: 10.3390/diagnostics14232698.
2
Building machine learning prediction models for well-being using predictors from the exposome and genome in a population cohort.在人群队列中,利用来自暴露组和基因组的预测因子构建用于健康状况的机器学习预测模型。
Nat Ment Health. 2024;2(10):1217-1230. doi: 10.1038/s44220-024-00294-2. Epub 2024 Aug 14.
3
Review: Cancer and neurodevelopmental disorders: multi-scale reasoning and computational guide.

本文引用的文献

1
A method for accurate group difference detection by constraining the mixing coefficients in an ICA framework.一种通过在独立成分分析(ICA)框架中约束混合系数来进行准确组间差异检测的方法。
Hum Brain Mapp. 2009 Sep;30(9):2953-70. doi: 10.1002/hbm.20721.
2
Association analysis of the glutamic acid decarboxylase 2 and the glutamine synthetase genes (GAD2, GLUL) with schizophrenia.谷氨酸脱羧酶2和谷氨酰胺合成酶基因(GAD2、GLUL)与精神分裂症的关联分析
Psychiatr Genet. 2009 Feb;19(1):6-13. doi: 10.1097/YPG.0b013e328311875d.
3
Machine learning classifiers and fMRI: a tutorial overview.
综述:癌症与神经发育障碍:多尺度推理与计算指南。
Front Cell Dev Biol. 2024 Jul 2;12:1376639. doi: 10.3389/fcell.2024.1376639. eCollection 2024.
4
A Systematic Review of Genetics- and Molecular-Pathway-Based Machine Learning Models for Neurological Disorder Diagnosis.基于遗传学和分子途径的机器学习模型在神经障碍诊断中的系统评价
Int J Mol Sci. 2024 Jun 11;25(12):6422. doi: 10.3390/ijms25126422.
5
Advancing Glaucoma Care: Integrating Artificial Intelligence in Diagnosis, Management, and Progression Detection.青光眼护理进展:将人工智能整合到诊断、管理和病情进展检测中。
Bioengineering (Basel). 2024 Jan 26;11(2):122. doi: 10.3390/bioengineering11020122.
6
Computational ensemble expert system classification for the recognition of bruxism using physiological signals.基于生理信号的磨牙症识别的计算集成专家系统分类
Heliyon. 2024 Feb 10;10(4):e25958. doi: 10.1016/j.heliyon.2024.e25958. eCollection 2024 Feb 29.
7
Copy Number Variation Informs fMRI-based Prediction of Autism Spectrum Disorder.拷贝数变异有助于基于功能磁共振成像的自闭症谱系障碍预测。
Mach Learn Clin Neuroimaging (2023). 2023 Oct;14312:133-142. doi: 10.1007/978-3-031-44858-4_13. Epub 2023 Oct 1.
8
Sampling inequalities affect generalization of neuroimaging-based diagnostic classifiers in psychiatry.抽样不等式会影响基于神经影像学的精神病学诊断分类器的泛化。
BMC Med. 2023 Jul 3;21(1):241. doi: 10.1186/s12916-023-02941-4.
9
Evaluation of Risk of Bias in Neuroimaging-Based Artificial Intelligence Models for Psychiatric Diagnosis: A Systematic Review.基于神经影像学的人工智能模型在精神疾病诊断中的偏倚风险评估:系统综述。
JAMA Netw Open. 2023 Mar 1;6(3):e231671. doi: 10.1001/jamanetworkopen.2023.1671.
10
Prediction of transition to psychosis from an at-risk mental state using structural neuroimaging, genetic, and environmental data.利用结构神经影像学、基因和环境数据预测处于精神病风险状态者向精神病的转变。
Front Psychiatry. 2023 Jan 19;13:1086038. doi: 10.3389/fpsyt.2022.1086038. eCollection 2022.
机器学习分类器与功能磁共振成像:教程概述
Neuroimage. 2009 Mar;45(1 Suppl):S199-209. doi: 10.1016/j.neuroimage.2008.11.007. Epub 2008 Nov 21.
4
A review of group ICA for fMRI data and ICA for joint inference of imaging, genetic, and ERP data.功能磁共振成像数据的独立成分分析及成像、基因和事件相关电位数据联合推断的独立成分分析综述。
Neuroimage. 2009 Mar;45(1 Suppl):S163-72. doi: 10.1016/j.neuroimage.2008.10.057. Epub 2008 Nov 13.
5
A genome-wide association study of schizophrenia using brain activation as a quantitative phenotype.一项以大脑激活作为定量表型的精神分裂症全基因组关联研究。
Schizophr Bull. 2009 Jan;35(1):96-108. doi: 10.1093/schbul/sbn155. Epub 2008 Nov 20.
6
Combining gene expression, demographic and clinical data in modeling disease: a case study of bipolar disorder and schizophrenia.在疾病建模中整合基因表达、人口统计学和临床数据:双相情感障碍和精神分裂症的案例研究
BMC Genomics. 2008 Nov 7;9:531. doi: 10.1186/1471-2164-9-531.
7
MTHFR 677C --> T genotype disrupts prefrontal function in schizophrenia through an interaction with COMT 158Val --> Met.亚甲基四氢叶酸还原酶(MTHFR)677C→T基因型通过与儿茶酚-O-甲基转移酶(COMT)158Val→Met相互作用破坏精神分裂症患者的前额叶功能。
Proc Natl Acad Sci U S A. 2008 Nov 11;105(45):17573-8. doi: 10.1073/pnas.0803727105. Epub 2008 Nov 6.
8
Association between a disrupted-in-schizophrenia 1 (DISC1) single nucleotide polymorphism and schizophrenia in a combined Scandinavian case-control sample.斯堪的纳维亚病例对照联合样本中精神分裂症断裂基因1(DISC1)单核苷酸多态性与精神分裂症的关联
Schizophr Res. 2008 Dec;106(2-3):237-41. doi: 10.1016/j.schres.2008.08.024. Epub 2008 Sep 24.
9
Genetic associations with schizophrenia: meta-analyses of 12 candidate genes.精神分裂症的基因关联:12个候选基因的荟萃分析
Schizophr Res. 2008 Sep;104(1-3):96-107. doi: 10.1016/j.schres.2008.06.016. Epub 2008 Aug 20.
10
Endophenotypes, dimensions, risks: is psychosis analogous to common inherited medical illnesses?内表型、维度、风险:精神病与常见的遗传性内科疾病类似吗?
Clin EEG Neurosci. 2008 Apr;39(2):73-7. doi: 10.1177/155005940803900210.