AI Chat Paper
Note: Please note that the following content is generated by AMiner AI. SciOpen does not take any responsibility related to this content.
{{lang === 'zh_CN' ? '文章概述' : 'Summary'}}
{{lang === 'en_US' ? '中' : 'Eng'}}
Chat more with AI
Article Link
Collect
Submit Manuscript
Show Outline
Outline
Show full outline
Hide outline
Outline
Show full outline
Hide outline
Regular Paper

An Efficient WRF Framework for Discovering Risk Genes and Abnormal Brain Regions in Parkinson's Disease Based on Imaging Genetics Data

College of Information Science and Engineering, Hunan Normal University, Changsha 410006, China
Hunan Provincial Key Laboratory of Intelligent Computing and Language Information Processing, Hunan Normal University, Changsha 410006, China
Show Author Information

Abstract

As an emerging research field of brain science, multimodal data fusion analysis has attracted broader attention in the study of complex brain diseases such as Parkinson's disease (PD). However, current studies primarily lie with detecting the association among different modal data and reducing data attributes. The data mining method after fusion and the overall analysis framework are neglected. In this study, we propose a weighted random forest (WRF) model as the feature screening classifier. The interactions between genes and brain regions are detected as input multimodal fusion features by the correlation analysis method. We implement sample classification and optimal feature selection based on WRF, and construct a multimodal analysis framework for exploring the pathogenic factors of PD. The experimental results in Parkinson's Progression Markers Initiative (PPMI) database show that WRF performs better compared with some advanced methods, and the brain regions and genes related to PD are detected. The fusion of multi-modal data can improve the classification of PD patients and detect the pathogenic factors more comprehensively, which provides a novel perspective for the diagnosis and research of PD. We also show the great potential of WRF to perform the multimodal data fusion analysis of other brain diseases.

Electronic Supplementary Material

Download File(s)
jcst-36-2-361-Highlights.pdf (125.5 KB)

References

[1]

Arkinson C, Walden H. Parkin function in Parkinson's disease. Science, 2018, 360(6386): 267-268. https://doi.org/10.1126/science.aar6606.

[2]

Lv D J, Li L X, Chen J, Wei S Z, Wang F, Hu H, Xie A M, Liu C F. Sleep deprivation caused a memory defects and emotional changes in a rotenone-based zebrafish model of Parkinson's disease. Behavioural Brain Research, 2019, 372: Article No. 112031. https://doi.org/10.1016/j.bbr.2019.112031.

[3]

Koros C, Simitsi A, Stefanis L. Genetics of Parkinson's disease: Genotype-phenotype correlations. International Review of Neurobiology, 2017, 132: 197-231. https://doi.org/10.1016/bs.irn.2017.01.009.

[4]

Kim M, Kim J, Lee S H, Park H. Imaging genetics approach to Parkinson's disease and its correlation with clinical score. Scientific Reports, 2017, 7: Article No. 46700. https://doi.org/10.1038/srep46700.

[5]

Won J H, Kim M, Park B Y, Youn J, Park H. Effectiveness of imaging genetics analysis to explain degree of depression in Parkinson's disease. PLoS ONE, 2019, 14(2): Article No. e0211699. https://doi.org/10.1371/journal.pone.0211699.

[6]

Wang X, Yan J, Yao X et al. Longitudinal genotype-phenotype association study through temporal structure auto-learning predictive model. Journal of Computational Biology, 2018, 25(7): 809-824. https://doi.org/10.1089/cmb.2018.0008.

[7]

Hao X, Li C, Yan J, Yao X, Risacher S L, Saykin A J, Shen L, Zhang D, Alzheimer's Disease Neuroimaging Initiative. Identification of associations between genotypes and longitudinal phenotypes via temporally-constrained group sparse canonical correlation analysis. Bioinformatics, 2017, 33(14): i341-i349. https://doi.org/10.1093/bioinformatics/btx245.

[8]

Min W, Liu J, Zhang S. Edge-group sparse PCA for network-guided high dimensional data analysis. Bioinformatics, 2018, 34(20): 3479-3487. https://doi.org/10.1093/bioinformatics/bty362.

[9]

Hua K, Zhang X. Estimating the total genome length of a metagenomic sample using k-mers. BMC Genomics, 2019, 20(2): Article No. 183. https://doi.org/10.1186/s12864-019-5467-x.

[10]

Calhoun V D, Liu J, AdalıT. A review of group ICA for fMRI data and ICA for joint inference of imaging, genetic, and ERP data. NeuroImage, 2009, 45(1, Supplement 1): S163-S172. https://doi.org/10.1016/j.neuroimage.2008.10.057.

[11]

Hamza T H, Zabetian C P, Tenesa A et al. Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease. Nature Genetics, 2010, 42(9): 781-785. https://doi.org/10.1038/ng.642.

[12]

Peng J, Guan J, Shang X. Predicting Parkinson's disease genes based on Node2vec and autoencoder. Frontiers in Genetics, 2019, 10: Article No. 226. https://doi.org/10.3389/fgene.2019.00226.

[13]

Mohammed A, Zamani M, Bayford R, Demosthenous A. Toward on-demand deep brain stimulation using online Parkinson's disease prediction driven by dynamic detection. IEEE Transactions on Neural Systems and Rehabilitation Engineering, 2017, 25(12): 2441-2452. https://doi.org/10.1109/TNSRE.2017.2722986.

[14]

Rana B, Juneja A, Saxena M, Gudwani S, Kumaran S S, Behari M, Agrawal R K. Relevant 3D local binary pattern based features from fused feature descriptor for differential diagnosis of Parkinson's disease using structural MRI. Biomedical Signal Processing and Control, 2017, 34: 134-143. https://doi.org/10.1016/j.bspc.2017.01.007.

[15]

Gupta D, Julka A, Jain S, Aggarwal T, Khanna A, Arunkumar N, De Albuquerque V H C. Optimized cuttlefish algorithm for diagnosis of Parkinson's disease. Cognitive Systems Research, 2018, 52: 36-48. https://doi.org/10.1016/j.cogsys.2018.06.006.

[16]

Zeng W, Liu F, Wang Q, Wang Y, Ma L, Zhang Y. Parkinson's disease classification using gait analysis via deterministic learning. Neuroscience Letters, 2016, 633: 268-278. https://doi.org/10.1016/j.neulet.2016.09.043.

[17]
Huang Y A, Huang Z A, You Z H, Hu P, Li L P, Li Z W, Wang L. Precise prediction of pathogenic microorganisms using 16S rRNA gene sequences. In Proc. the 15th International Conference on Intelligent Computing, August 2019, pp.138-150. https://doi.org/10.1007/978-3-030-26969-2_13.
[18]

Du L, Liu K, Zhang T, Yao X, Yan J, Risacher S L, Han J, Guo L, Saykin A J, Shen L, Alzheimer's Disease Neuroimaging Initiative. A novel SCCA approach via truncated 1-norm and truncated group lasso for brain imaging genetics. Bioinformatics, 2017, 34(2): 278-285. https://doi.org/10.1093/bioinformatics/btx594.

[19]

Du L, Liu K, Zhu L, Yao X, Risacher S L, Guo L, Saykin A J, Shen L, Alzheimer's Disease Neuroimaging Initiative. Identifying progressive imaging genetic patterns via multitask sparse canonical correlation analysis: A longitudinal study of the ADNI cohort. Bioinformatics, 2019, 35(14): i474-i483. https://doi.org/10.1093/bioinformatics/btz320.

[20]

Du L, Liu K, Yao X, Risacher S L, Shen L. Detecting genetic associations with brain imaging phenotypes in Alzheimer's disease via a novel structured SCCA approach. Medical Image Analysis, 2020, 61: Article No. 101656. https://doi.org/10.1016/j.media.2020.101656.

[21]

Wei L, Su R, Luan S, Liao Z, Manavalan B, Zou Q, Shi X. Iterative feature representations improve N4-methylcytosine site prediction. Bioinformatics, 2019, 35(23): 4930-4937. https://doi.org/10.1093/bioinformatics/btz408.

[22]

Chen F X, Kang D Z, Chen F Y, Liu Y, Wu G, Li X, Yu L H, Lin Y X, Lin Z Y. Gray matter atrophy associated with mild cognitive impairment in Parkinson's disease. Neuroscience Letters, 2016, 617: 160-165. https://doi.org/10.1016/j.neulet.2015.12.055.

[23]

Guimarães R P, Arci Santos M C, Dagher A et al. Pattern of reduced functional connectivity and structural abnormalities in Parkinson's disease: An exploratory study. Frontiers in Neurology, 2017, 7: 243. https://doi.org/10.3389/fneur.2016.00243.

[24]

Hou Y, Wei Q, Ou R, Yang J, Song W, Gong Q, Shang H. Impaired topographic organization in cognitively unimpaired drug-naïve patients with rigidity-dominant Parkinson’ disease. Parkinsonism & Related Disorders, 2018, 56: 52-57. https://doi.org/10.1016/j.parkreldis.2018.06.021.

[25]

Zhao L, Wang E, Zhang X et al. Cortical structural connectivity alterations in primary insomnia: Insights from MRI-based morphometric correlation analysis. BioMed Research International, 2015, 2015: Article No. 817595. https://doi.org/10.1155/2015/817595.

[26]

Meunier D, Stamatakis E A, Tyler L K. Age-related functional reorganization, structural changes, and preserved cognition. Neurobiology of Aging, 2014, 35(1): 42-54. https://doi.org/10.1016/j.neurobiolaging.2013.07.003.

[27]

Li H F, Yang L, Yin D, Chen W J, Liu G L, Ni W, Wang N, Yu W, Wu Z Y, Wang Z. Associations between neuroanatomical abnormality and motor symptoms in paroxysmal kinesigenic dyskinesia. Parkinsonism & Related Disorders, 2019, 62: 134-140. https://doi.org/10.1016/j.parkreldis.2018.12.029.

[28]

Reijnders J S A M, Scholtissen B, Weber W E J, Aalten P, Verhey F R J, Leentjens A F G. Neuroanatomical correlates of apathy in Parkinson's disease: A magnetic resonance imaging study using voxel-based morphometry. Movement Disorders, 2010, 25(14): 2318-2325. https://doi.org/10.1002/mds.23268.

[29]

Melzer T R, Watts R, MacAskill M R, Pitcher T L, Livingston L, Keenan R J, Dalrymple-Alford J C, Anderson T J. Grey matter atrophy in cognitively impaired Parkinson's disease. Journal of Neurology, Neurosurgery, and Psychiatry, 2012, 83(2): 188-194. https://doi.org/10.1136/jnnp-2011-300828.

[30]

De Schipper L J, Hafkemeijer A, van der Grond J, Marinus J, Henselmans J M L, van Hilten J J. Altered whole-brain and network-based functional connectivity in Parkinson's disease. Frontiers in Neurology, 2018, 9: Article No. 419. https://doi.org/10.3389/fneur.2018.00419.

[31]

Evangelisti S, Pittau F, Testa C et al. L-dopa modulation of brain connectivity in Parkinson's disease patients: A pilot EEG-fMRI study. Frontiers in Neuroscience, 2019, 13: Article No. 611. https://doi.org/10.3389/fnins.2019.00611.

[32]

Wang Q, Li W X, Dai S X, Guo Y C, Han F F, Zheng J J, Li G H, Huang J F. Meta-analysis of Parkinson's disease and Alzheimer's disease revealed commonly impaired pathways and dysregulation of NRF2-dependent genes. Journal of Alzheimer's Disease, 2017, 56(4): 1525-1539. https://doi.org/10.3233/JAD-161032.

[33]

International Parkinson Disease Genomics Consortium. Imputation of sequence variants for identification of genetic risks for Parkinson's disease: A meta-analysis of genome-wide association studies. The Lancet, 2011, 377(9766): 641-649. https://doi.org/10.1016/S0140-6736(10)62345-8.

[34]

Ahmed I, Tamouza R, Delord M et al. Association between Parkinson's disease and the HLA-DRB1 locus. Movement Disorders, 2012, 27(9): 1104-1110. https://doi.org/10.1002/mds.25035.

[35]

Bao W, Jiang Z, Huang D S. Novel human microbe-disease association prediction using network consistency projection. BMC Bioinformatics, 2017, 18(16): Article No. 543. https://doi.org/10.1186/s12859-017-1968-2.

[36]

Sivaranjini S, Sujatha C M. Deep learning based diagnosis of Parkinson's disease using convolutional neural network. Multimedia Tools and Applications, 2019, 79(3): 15467–15479. https://doi.org/10.1007/s11042-019-7469-8.

[37]
Martinez-Murcia F J, Ortiz A, Gorriz J M, Ramirez J, Castillo-Barnes D, Salas-Gonzalez D, Segovia F. Deep convolutional autoencoders vs PCA in a highly-unbalanced Parkinson's disease dataset: A DaTSCAN study. In Proc. the 13th International Conference on Soft Computing Models in Industrial and Environmental Applications, June 2018, pp. 47-56. https://doi.org/10.1007/978-3-319-94120-2_5.
[38]

Gao C, Sun H, Wang T et al. Model-based and model-free machine learning techniques for diagnostic prediction and classification of clinical outcomes in Parkinson's disease. Scientific Reports, 2018, 8(1): Article No. 7129. https://doi.org/10.1038/s41598-018-24783-4.

[39]

Abós A, Baggio H C, Segura B, García-Díaz A I, Compta Y, Martí M J, Valldeoriola F, Junqué C. Discriminating cognitive status in Parkinson's disease through functional connectomics and machine learning. Scientific Reports, 2017, 7: Article No. 45347. https://doi.org/10.1038/srep45347.

[40]

Niu Y W, Wang G H, Yan G Y, Chen X. Integrating random walk and binary regression to identify novel miRNA-disease association. BMC Bioinformatics, 2019, 20(1): Article No. 59. https://doi.org/10.1186/s12859-019-2640-9.

[41]

Zhao Y, Chen X, Yin J. Adaptive boosting-based computational model for predicting potential miRNA-disease associations. Bioinformatics, 2019, 35(22): 4730-4738. https://doi.org/10.1093/bioinformatics/btz297.

Journal of Computer Science and Technology
Pages 361-374
Cite this article:
Bi X-A, Xing Z-X, Xu R-H, et al. An Efficient WRF Framework for Discovering Risk Genes and Abnormal Brain Regions in Parkinson's Disease Based on Imaging Genetics Data. Journal of Computer Science and Technology, 2021, 36(2): 361-374. https://doi.org/10.1007/s11390-021-0801-6

361

Views

1

Crossref

1

Web of Science

1

Scopus

0

CSCD

Altmetrics

Received: 14 July 2020
Accepted: 28 February 2021
Published: 05 March 2021
©Institute of Computing Technology, Chinese Academy of Sciences 2021
Return