Application of Empirical Mode Decomposition (EMD) on DaTSCAN SPECT images to explore Parkinson Disease
Highlights
► Procedure to classify DaTSCAN images using Empirical Mode Decomposition (EMD). ► Intensity normalization and filtering, PCA and SVM are used in combination with EMD. ► This approach outperforms the voxel-as-features method used as a baseline. ► Acc, Sen and Spe are highly improved (above 90%) and fairly stable on final tests.
Introduction
Parkinsonian Syndrome (PS) or Parkinsonism is one of the most common neurodegenerative disorders, characterized by the presence of hypokinesia associated with rest tremor, rigidity or postural instability. Parkinsonism is commonly caused by Parkinson’s Disease (PD), a neurodegenerative disease which originates due to progressive loss of dopaminergic neurons of the nigrostriatal pathway. This cell loss involves a substantial decrease in the dopamine content of the striatum and a loss of dopamine transporters (Booij et al., 1997). Up to 2% population over 65 years suffer from PD and about 20–25% of all are not correctly diagnosed.
I-ioflupane (better known as DaTSCAN) is a neuroimaging radiopharmaceutical drug used to assist the diagnosis of Parkinsonism. This drug binds to the dopamine transporters in the striatum. Dopamine transporters (DAT) are proteins situated at the presynaptic terminal of dopaminergic neurons which are responsible for the re-uptake of dopamine. In order to obtain the distribution of the radiopharmaceutical in the brain and visualize the loss of dopamine, a Single-Proton Emission Computed Tomography (SPECT) camera is used (Booij et al., 1997, Winogrodzka et al., 2003). The SPECT maps obtained are normally examined by experts on PS diagnosis (Lozano, del Valle Torres, García, Cardo, & Arillo, 2007). These experts often use proprietary software to delimit Regions Of Interest (ROIs) and quantify the radiopharmaceutical uptake (Górriz et al., 2011, Jennings et al., 2004, Ortega Lozano et al., 2010, Pirker et al., 2000). This procedure is subjective and prone to errors since it relies on gross changes in transporter density throughout the ROI (Salas-Gonzalez et al., 2010). As such, it may not be sensitive to changes in the pattern of distribution that can characterize the progression of the disease (Scherfler & Nocker, 2009).
Recently some methods based on the machine learning paradigm have been applied to image analysis procedures, developing CAD systems for several neurodegenerative diseases (Seppi et al., 2006, Zubal et al., 2007), just like Alzheimer Disease or Parkinson Disease (Illán et al., 2012, Segovia et al., 2012). This CAD system is used for the extraction of complex high-dimensional features of the images that will be used to train the automatic classifier SVM to discriminate between normal and pathological controls (Illán et al., 2010, Illán et al., 2012, Ramírez et al., 2009), performing thus an automatic diagnosis (Chaves et al., 2012, Chaves et al., 2011, Chaves et al., 2012, Chaves et al., 2011, Martı´nez-Murcia et al., 2012, Ortiz et al., 2011).
The aim of this work is to continue the work undertaken by Gallix, Górriz, Ramírez, ÁIllán, and Lang (2012) and evaluate the performance of an adaptative image decomposition technique based on EMD (Zeiler et al., 2010). For this purpose we make use of different methods. Firstly we apply a preprocessing method consisting on an intensity normalization and a gaussian filtering of the images to remove noise added by the image reconstruction system in the Hospital. Once the noise is removed, images are decomposed with EMD and filtered again. Finally we make use of Principal Component Analysis (PCA) (Maćkiewicz and Ratajczak, 1993, Moore, 1981) and Independent Component Analysis (ICA) (Hyvärinen, 1999b) to extract their features and classify with a Support Vector Machines (SVM) method (Martínez et al., 2010, Segovia et al., 2012, Vapnik, 1998) as shown in Fig. 1.
This article is organized as follows. In Section 2 the image acquisition, preprocessing, adaptative image decomposition technique (EMD), feature extraction and classification methods used in this work are presented. In Section 3 we describe the experiment proposed, comparing the results obtained with the baseline results (VAF). Results are discussed in Section 3 too, and finally, conclusions are shown in Section 4.
Section snippets
Database
The images were obtained after a period of three hours after the intravenous injection of 111–185 MBq of I-123-Ioflupane, with prior thyroid blocking with Lugol’s solution. The tomographic study (SPECT) with Ioflupane/FP-CIT-I-123 was performed using a triple-head gamma-camera (Picker 3000), equipped with collimators for a low-energy and ultra high-resolution neurofan beam (Leuhr-NeuroFan). A 360° circular orbit was made around the cranium, with a rotation radius of 12.9–13.2 cm, step and shoot
Experiments and results
For all the experiments, we have used part of the database previously described, focussing on Axial slices. Thus, from the beginning we have 80 patients with 45 different slices each one. Within those 45 slices we have selected only 21 central slices (Fig. 3) because slices from the extrema have deficiencies and a significant lack of information.
Six experiments were performed considering different preprocessing and post-processing methods:
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Experiment I:
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Preprocess: No intensity normalization,
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Conclusion
In this paper, a new approach to Computed Aided Diagnosis (CAD) for Parkinsonian Syndrome (PS) is proposed. Once reviewed and analysed the results of all available options, the one who gives a better performance is obtained by applying an intensity normalization to the maximum and a Gaussian Filter before MEEMD, after the decomposition, IMFs and residue are filtered with a Gaussian filter, and then a feature selection and extraction is done prior to classification, which corresponds to
Acknowledgments
This work was partly supported by the MICINN under the TEC2008-02113 project and the Consejera de Innovacin, Ciencia y Empresa (Junta de Andalucía, Spain) under the Excellence Projects P07-TIC-02566, P09-TIC-4530, P11-TIC-7103, P11-TIC-7103 and TEC2012–34306
We are grateful to M. Gómez-Río and coworkers from the Virgen de las Nieves hospital in Granada (Spain) for providing and labeling the SPECT images used in this work.
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