What can artificial neural networks teach us about neurodegenerative disorders with extrapyramidal features?

被引:17
|
作者
Litvan, I
DeLeo, JM
Hauw, JJ
Daniel, SE
Jellinger, K
McKee, A
Dickson, D
Horoupian, DS
Lantos, PL
Tabaton, M
机构
[1] NIH, DIV COMP RES & TECHNOL, BETHESDA, MD 20892 USA
[2] MASSACHUSETTS GEN HOSP, DEPT NEUROPATHOL, BOSTON, MA 02114 USA
[3] ALBERT EINSTEIN COLL MED, DEPT NEUROPATHOL, NEW YORK, NY USA
[4] STANDFORD SCH MED, DEPT PATHOL NEUROPATHOL, STANFORD, CA USA
[5] CASE WESTERN RESERVE UNIV, DIV NEUROPATHOL, CLEVELAND, OH 44106 USA
[6] HOP LA PITIE SALPETRIERE, ASSOC CLAUDE BERNARD, INSERM U360, RAYMOND ESCOUROLLE NEUROPATHOL LAB, PARIS, FRANCE
[7] LUDWIG BOLTZMANN INST CLIN NEUROBIOL, VIENNA, AUSTRIA
[8] INST PSYCHIAT, PARKINSONS DIS SOC BRAIN TISSUE BANK, LONDON, ENGLAND
[9] INST PSYCHIAT, INST NEUROL, DEPT NEUROPATHOL, LONDON, ENGLAND
基金
英国医学研究理事会;
关键词
artificial neural networks; dystal; neurodegenerative disorders; neuropathology; progressive supranuclear palsy;
D O I
10.1093/brain/119.3.831
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Artificial neural networks (ANNs), computer paradigms that can learn, excel in pattern recognition tasks such as disease diagnosis. Artificial neural networks operate in two different learning modes: supervised, in which a known diagnostic outcome is presented to the ANN, and unsupervised, in which the diagnostic outcome is not presented. A supervised learning ANN could emulate human expert diagnostic performance and identify relevant predictive markers in the diagnostic task, while an unsupervised learning ANN could suggest reasonable alternative diagnostic classification criteria. In the present study, we used ANN methodology to try to overcome the neuropathological difficulties in differentiating the subtypes of progressive supranuclear palsy (PSP), and in differentiating PSP from postencephalitic parkinsonism (PEP) and corticobasal degeneration, or Pick's disease from corticobasal degeneration. First, we applied supervised learning ANN to classify 62 cases of these disorders and to identify diagnostic markers that distinguish them. In a second experiment, we used unsupervised learning ANN to investigate possible alternative nosological classifications. Artificial neural networks input data for each case consisted of values representing histological features, including neurofibrillary tangles, neuronal loss and gliosis found in multiple brain sampling areas. The supervised learning ANN achieved excellent accuracy in classifying PSP but had difficulty classifying the other disorders. This method identified a few features that might help to differentiate PEP, supported currently proposed criteria for Pick's disease, corticobasal degeneration and typical PSP, but detected no features to characterize the atypical subtype of PSP. In general, unsupervised learning ANN supported the present nosological classification for PSP, PEP, Pick's disease and corticobasal degeneration, although it overlapped some groups. Artificial neural networks methodology appears promising for studying neurodegenerative disorders.
引用
收藏
页码:831 / 839
页数:9
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