Preprocessing of 18F-DMFP-PET Data Based on Hidden Markov Random Fields and the Gaussian Distribution

18F-DMFP-PET is an emerging neuroimaging modality used to diagnose Parkinson's disease (PD) that allows us to examine postsynaptic dopamine D2/3 receptors. Like other neuroimaging modalities used for PD diagnosis, most of the total intensity of 18F-DMFP-PET images is concentrated in the striatum. However, other regions can also be useful for diagnostic purposes. An appropriate delimitation of the regions of interest contained in 18F-DMFP-PET data is crucial to improve the automatic diagnosis of PD. In this manuscript we propose a novel methodology to preprocess 18F-DMFP-PET data that improves the accuracy of computer aided diagnosis systems for PD. First, the data were segmented using an algorithm based on Hidden Markov Random Field. As a result, each neuroimage was divided into 4 maps according to the intensity and the neighborhood of the voxels. The maps were then individually normalized so that the shape of their histograms could be modeled by a Gaussian distribution with equal parameters for all the neuroimages. This approach was evaluated using a dataset with neuroimaging data from 87 parkinsonian patients. After these preprocessing steps, a Support Vector Machine classifier was used to separate idiopathic and non-idiopathic PD. Data preprocessed by the proposed method provided higher accuracy results than the ones preprocessed with previous approaches.

[1]  V. Dhawan,et al.  Changes in network activity with the progression of Parkinson's disease. , 2007, Brain : a journal of neurology.

[2]  Jogeshwar Mukherjee,et al.  Striatal and extrastriatal microPET imaging of D2/D3 dopamine receptors in rat brain with [18F]fallypride and [18F]desmethoxyfallypride , 2011, Synapse.

[3]  Juan Manuel Górriz,et al.  Distinguishing Parkinson's disease from atypical parkinsonian syndromes using PET data and a computer system based on support vector machines and Bayesian networks , 2015, Front. Comput. Neurosci..

[4]  R. Prashanth,et al.  Automatic classification and prediction models for early Parkinson's disease diagnosis from SPECT imaging , 2014, Expert Syst. Appl..

[5]  Robert P. W. Duin,et al.  Classifiers in almost empty spaces , 2000, Proceedings 15th International Conference on Pattern Recognition. ICPR-2000.

[6]  M. Sawada,et al.  Biochemistry of postmortem brains in Parkinson's disease: historical overview and future prospects. , 2007, Journal of neural transmission. Supplementum.

[7]  Francesco Giammarile,et al.  New strategy for automatic tumor segmentation by adaptive thresholding on PET/CT images , 2012, Journal of applied clinical medical physics.

[8]  Javier Ramírez,et al.  Linear intensity normalization of FP-CIT SPECT brain images using the α-stable distribution , 2013, NeuroImage.

[9]  Juan Manuel Górriz,et al.  GMM based SPECT image classification for the diagnosis of Alzheimer's disease , 2011, Appl. Soft Comput..

[10]  A. Hartmann Postmortem studies in Parkinson's disease , 2004, Dialogues in clinical neuroscience.

[11]  Karl J. Friston,et al.  CHAPTER 6 – Segmentation , 2007 .

[12]  Päivi Marjamäki,et al.  A post-mortem study on striatal dopamine receptors in Parkinson's disease , 1991, Brain Research.

[13]  Richard S. J. Frackowiak,et al.  Cerebral blood flow, blood volume and oxygen utilization. Normal values and effect of age. , 1990, Brain : a journal of neurology.

[14]  J. M. GÓRRIZ,et al.  Case-Based Statistical Learning: A Non-Parametric Implementation With a Conditional-Error Rate SVM , 2017, IEEE Access.

[15]  F Segovia,et al.  Improved Parkinsonism diagnosis using a partial least squares based approach. , 2012, Medical physics.

[16]  Janaina Mourão Miranda,et al.  PRoNTo: Pattern Recognition for Neuroimaging Toolbox , 2013, Neuroinformatics.

[17]  Juan Manuel Górriz,et al.  Automatic detection of Parkinsonism using significance measures and component analysis in DaTSCAN imaging , 2014, Neurocomputing.

[18]  Albert Gjedde,et al.  Data-driven intensity normalization of PET group comparison studies is superior to global mean normalization , 2009, NeuroImage.

[19]  Karl J. Friston,et al.  Incorporating Prior Knowledge into Image Registration , 1997, NeuroImage.

[20]  R. Buchert,et al.  [18F]FDG-PET is superior to [123I]IBZM-SPECT for the differential diagnosis of parkinsonism , 2012, Neurology.

[21]  F. Segovia,et al.  Classification of functional brain images using a GMM-based multi-variate approach , 2010, Neuroscience Letters.

[22]  F. Niccolini,et al.  Dopamine receptor mapping with PET imaging in Parkinson’s disease , 2014, Journal of Neurology.

[23]  Hellmuth Obrig,et al.  Reference Cluster Normalization Improves Detection of Frontotemporal Lobar Degeneration by Means of FDG-PET , 2012, PloS one.

[24]  F Segovia,et al.  Automatic assistance to Parkinson's disease diagnosis in DaTSCAN SPECT imaging. , 2012, Medical physics.

[25]  Paul Cumming,et al.  The Value of the Dopamine D2/3 Receptor Ligand 18F-Desmethoxyfallypride for the Differentiation of Idiopathic and Nonidiopathic Parkinsonian Syndromes , 2010, Journal of Nuclear Medicine.

[26]  Richard Simon,et al.  Bias in error estimation when using cross-validation for model selection , 2006, BMC Bioinformatics.

[27]  Stephen M. Smith,et al.  Segmentation of brain MR images through a hidden Markov random field model and the expectation-maximization algorithm , 2001, IEEE Transactions on Medical Imaging.

[28]  Barry Horwitz,et al.  An Automatic Threshold-Based Scaling Method for Enhancing the Usefulness of Tc-HMPAO SPECT in the Diagnosis of Alzheimer's Disease , 1998, MICCAI.

[29]  Vladimir N. Vapnik,et al.  The Nature of Statistical Learning Theory , 2000, Statistics for Engineering and Information Science.

[30]  Kai Boetzel,et al.  Multivariate Analysis of 18F-DMFP PET Data to Assist the Diagnosis of Parkinsonism , 2017, Front. Neuroinform..

[31]  Andrea Bergmann,et al.  Statistical Parametric Mapping The Analysis Of Functional Brain Images , 2016 .

[32]  T. Vogt,et al.  The dopamine D2 receptor ligand 18F-desmethoxyfallypride: an appropriate fluorinated PET tracer for the differential diagnosis of parkinsonism , 2004, European Journal of Nuclear Medicine and Molecular Imaging.

[33]  Christophe Phillips,et al.  Multiclass classification of FDG PET scans for the distinction between Parkinson's disease and atypical parkinsonian syndromes , 2013, NeuroImage: Clinical.

[34]  Jian Wang,et al.  Simultaneous tumor segmentation, image restoration, and blur kernel estimation in PET using multiple regularizations , 2017, Comput. Vis. Image Underst..

[35]  Perry E Radau,et al.  Clinical testing of an optimized software solution for an automated, observer-independent evaluation of dopamine transporter SPECT studies. , 2005, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[36]  J. Booij,et al.  [123I]FP-CIT SPECT is a useful method to monitor the rate of dopaminergic degeneration in early-stage Parkinson's disease , 2001, Journal of Neural Transmission.

[37]  U. Dillmann,et al.  Striatal FP-CIT uptake differs in the subtypes of early Parkinson’s disease , 2007, Journal of Neural Transmission.

[38]  K. S. Nijran,et al.  Automatic classification of 123I-FP-CIT (DaTSCAN) SPECT images , 2011, Nuclear medicine communications.