Pathological neural networks and artificial neural networks in ALS: diagnostic classification based on pathognomonic neuroimaging features

被引:51
作者
Bede, Peter [1 ,2 ]
Murad, Aizuri [1 ]
Hardiman, Orla [1 ]
机构
[1] Trinity Coll Dublin, Trinity Biomed Sci Inst, Computat Neuroimaging Grp, Room 5-43,Pearse St, Dublin 2, Ireland
[2] Sorbonne Univ, Pitie Salpetriere Univ Hosp, Paris, France
关键词
Neuroradiology; Machine learning; Amyotrophic lateral sclerosis; Neuroimaging; Artificial neural networks; AMYOTROPHIC-LATERAL-SCLEROSIS; CERVICAL CORD; BRAIN; WHITE; MRI; ATLAS; MIND;
D O I
10.1007/s00415-021-10801-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The description of group-level, genotype- and phenotype-associated imaging traits is academically important, but the practical demands of clinical neurology centre on the accurate classification of individual patients into clinically relevant diagnostic, prognostic and phenotypic categories. Similarly, pharmaceutical trials require the precision stratification of participants based on quantitative measures. A single-centre study was conducted with a uniform imaging protocol to test the accuracy of an artificial neural network classification scheme on a cohort of 378 participants composed of patients with ALS, healthy subjects and disease controls. A comprehensive panel of cerebral volumetric measures, cortical indices and white matter integrity values were systematically retrieved from each participant and fed into a multilayer perceptron model. Data were partitioned into training and testing and receiver-operating characteristic curves were generated for the three study-groups. Area under the curve values were 0.930 for patients with ALS, 0.958 for disease controls, and 0.931 for healthy controls relying on all input imaging variables. The ranking of variables by classification importance revealed that white matter metrics were far more relevant than grey matter indices to classify single subjects. The model was further tested in a subset of patients scanned within 6 weeks of their diagnosis and an AUC of 0.915 was achieved. Our study indicates that individual subjects may be accurately categorised into diagnostic groups in an observer-independent classification framework based on multiparametric, spatially registered radiology data. The development and validation of viable computational models to interpret single imaging datasets are urgently required for a variety of clinical and clinical trial applications.
引用
收藏
页码:2440 / 2452
页数:13
相关论文
共 83 条
[1]   Adaptive functional reorganization in amyotrophic lateral sclerosis: coexisting degenerative and compensatory changes [J].
Abidi, M. ;
de Marco, G. ;
Couillandre, A. ;
Feron, M. ;
Mseddi, E. ;
Termoz, N. ;
Querin, G. ;
Pradat, P. -F. ;
Bede, P. .
EUROPEAN JOURNAL OF NEUROLOGY, 2020, 27 (01) :121-128
[2]   Neural Correlates of Motor Imagery of Gait in Amyotrophic Lateral Sclerosis [J].
Abidi, Malek ;
de Marco, Giovanni ;
Grami, Fatma ;
Termoz, Nicolas ;
Couillandre, Annabelle ;
Querin, Giorgia ;
Bede, Peter ;
Pradat, Pierre-Francois .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2021, 53 (01) :223-233
[3]   Neuroimaging in amyotrophic lateral sclerosis: current and emerging uses [J].
Agosta, Federica ;
Spinelli, Edoardo Gioele ;
Filippi, Massimo .
EXPERT REVIEW OF NEUROTHERAPEUTICS, 2018, 18 (05) :395-406
[4]   Unraveling ALS due to SOD1 mutation through the combination of brain and cervical cord MRI [J].
Agosta, Federica ;
Spinelli, Edoardo Gioele ;
Marjanovic, Ivan V. ;
Stevic, Zorica ;
Pagani, Elisabetta ;
Valsasina, Paola ;
Salak-Djokic, Biljana ;
Jankovic, Milena ;
Lavrnic, Dragana ;
Kostic, Vladimir S. ;
Filippi, Massimo .
NEUROLOGY, 2018, 90 (08) :E707-E716
[5]   Structural brain correlates of cognitive and behavioral impairment in MND [J].
Agosta, Federica ;
Ferraro, Pilar M. ;
Riva, Nilo ;
Spinelli, Edoardo G. ;
Chio, Adriano ;
Canu, Elisa ;
Valsasina, Paola ;
Lunetta, Christian ;
Iannaccone, Sandro ;
Copetti, Massimiliano ;
Prudente, Evelina ;
Comi, Giancarlo ;
Falini, Andrea ;
Filippi, Massimo .
HUMAN BRAIN MAPPING, 2016, 37 (04) :1614-1626
[6]   MRI signatures of the frontotemporal lobar degeneration continuum [J].
Agosta, Federica ;
Galantucci, Sebastiano ;
Magnani, Giuseppe ;
Marcone, Alessandra ;
Martinelli, Daniele ;
Volonte, Maria Antonietta ;
Riva, Nilo ;
Iannaccone, Sandro ;
Ferraro, Pilar M. ;
Caso, Francesca ;
Chio, Adriano ;
Comi, Giancarlo ;
Falini, Andrea ;
Filippi, Massimo .
HUMAN BRAIN MAPPING, 2015, 36 (07) :2602-2614
[7]   Artificial neural networks in medical diagnosis [J].
Amato, Filippo ;
Lopez, Alberto ;
Pena-Mendez, Eladia Maria ;
Vanhara, Petr ;
Hampl, Ales ;
Havel, Josef .
JOURNAL OF APPLIED BIOMEDICINE, 2013, 11 (02) :47-58
[8]   Genotype-associated cerebellar profiles in ALS: focal cerebellar pathology and cerebro-cerebellar connectivity alterations [J].
Bede, Peter ;
Chipika, Rangariroyashe H. ;
Christidi, Foteini ;
Hengeveld, Jennifer C. ;
Karavasilis, Efstratios ;
Argyropoulos, Georgios D. ;
Lope, Jasmin ;
Li Hi Shing, Stacey ;
Velonakis, Georgios ;
Dupuis, Leonie ;
Doherty, Mark A. ;
Vajda, Alice ;
McLaughlin, Russell L. ;
Hardiman, Orla .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2021, 92 (11) :1197-1205
[9]   Consideration of C9orf72-associated ALS-FTD as a neurodevel-opmental disorder: insights from neuroimaging [J].
Bede, Peter ;
Siah, We Fong ;
McKenna, Mary Clare ;
Li Hi Shing, Stacey .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2020, 91 (11) :1138-1138
[10]   Brainstem pathology in amyotrophic lateral sclerosis and primary lateral sclerosis: A longitudinal neuroimaging study [J].
Bede, Peter ;
Chipika, Rangariroyashe H. ;
Finegan, Eoin ;
Shing, Stacey Li Hi ;
Doherty, Mark A. ;
Hengeveld, Jennifer C. ;
Vajda, Alice ;
Hutchinson, Siobhan ;
Donaghy, Colette ;
McLaughlin, Russell L. ;
Hardiman, Orla .
NEUROIMAGE-CLINICAL, 2019, 24