Artificial neural network based characterization of the volume of tissue activated during deep brain stimulation

被引:94
作者
Chaturvedi, Ashutosh [1 ,2 ]
Lujan, J. Luis [2 ]
McIntyre, Cameron C. [1 ,2 ]
机构
[1] Case Western Reserve Univ, Dept Biomed Engn, Cleveland, OH 44106 USA
[2] Cleveland Clin Fdn, Dept Biomed Engn, Cleveland, OH 44195 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1088/1741-2560/10/5/056023
中图分类号
R318 [生物医学工程];
学科分类号
100103 [病原生物学];
摘要
Objective. Clinical deep brain stimulation (DBS) systems can be programmed with thousands of different stimulation parameter combinations (e. g. electrode contact(s), voltage, pulse width, frequency). Our goal was to develop novel computational tools to characterize the effects of stimulation parameter adjustment for DBS. Approach. The volume of tissue activated (VTA) represents a metric used to estimate the spatial extent of DBS for a given parameter setting. Traditional methods for calculating the VTA rely on activation function (AF)-based approaches and tend to overestimate the neural response when stimulation is applied through multiple electrode contacts. Therefore, we created a new method for VTA calculation that relied on artificial neural networks (ANNs). Main results. The ANN-based predictor provides more accurate descriptions of the spatial spread of activation compared to AF-based approaches for monopolar stimulation. In addition, the ANN was able to accurately estimate the VTA in response to multi-contact electrode configurations. Significance. The ANN-based approach may represent a useful method for fast computation of the VTA in situations with limited computational resources, such as a clinical DBS programming application on a tablet computer.
引用
收藏
页数:8
相关论文
共 22 条
[1]
Boyd S.P, 2004, Convex optimization, DOI [DOI 10.1017/CBO9780511804441, 10.1017/CBO9780511804441]
[2]
Patient-speciftic analysis of the volume of tissue activated during deep brain stimulation [J].
Butson, Christopher R. ;
Cooper, Scott E. ;
Henderson, Jaimie M. ;
McIntyre, Cameron C. .
NEUROIMAGE, 2007, 34 (02) :661-670
[3]
Role of electrode design on the volume of tissue activated during deep brain stimulation [J].
Butson, Christopher R. ;
McIntyre, Cameron C. .
JOURNAL OF NEURAL ENGINEERING, 2006, 3 (01) :1-8
[4]
Sources and effects of electrode impedance during deep brain stimulation [J].
Butson, CR ;
Maks, CB ;
McIntyre, CC .
CLINICAL NEUROPHYSIOLOGY, 2006, 117 (02) :447-454
[5]
Tissue and electrode capacitance reduce neural activation volumes during deep brain stimulation [J].
Butson, CR ;
McIntyre, CC .
CLINICAL NEUROPHYSIOLOGY, 2005, 116 (10) :2490-2500
[6]
Patient-specific models of deep brain stimulation: Influence of field model complexity on neural activation predictions [J].
Chaturvedi, Ashutosh ;
Butson, Christopher R. ;
Lempka, Scott F. ;
Cooper, Scott E. ;
McIntyre, Cameron C. .
BRAIN STIMULATION, 2010, 3 (02) :65-77
[7]
Reversing cognitive-motor impairments in Parkinson's disease patients using a computational modelling approach to deep brain stimulation programming [J].
Frankemolle, Anneke M. M. ;
Wu, Jennifer ;
Noecker, Angela M. ;
Voelcker-Rehage, Claudia ;
Ho, Jason C. ;
Vitek, Jerrold L. ;
McIntyre, Cameron C. ;
Alberts, Jay L. .
BRAIN, 2010, 133 :746-761
[8]
The NEURON simulation environment [J].
Hines, ML ;
Carnevale, NT .
NEURAL COMPUTATION, 1997, 9 (06) :1179-1209
[9]
Automated Optimal Coordination of Multiple-DOF Neuromuscular Actions in Feedforward Neuroprostheses [J].
Lujan, J. Luis ;
Crago, Patrick E. .
IEEE TRANSACTIONS ON BIOMEDICAL ENGINEERING, 2009, 56 (01) :179-187
[10]
Spatial steering of deep brain stimulation volumes using a novel lead design [J].
Martens, H. C. F. ;
Toader, E. ;
Decre, M. M. J. ;
Anderson, D. J. ;
Vetter, R. ;
Kipke, D. R. ;
Baker, Kenneth B. ;
Johnson, Matthew D. ;
Vitek, Jerrold L. .
CLINICAL NEUROPHYSIOLOGY, 2011, 122 (03) :558-566