29 research outputs found

    Classification of interstitial lung disease patterns with topological texture features

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    Topological texture features were compared in their ability to classify morphological patterns known as 'honeycombing' that are considered indicative for the presence of fibrotic interstitial lung diseases in high-resolution computed tomography (HRCT) images. For 14 patients with known occurrence of honey-combing, a stack of 70 axial, lung kernel reconstructed images were acquired from HRCT chest exams. A set of 241 regions of interest of both healthy and pathological (89) lung tissue were identified by an experienced radiologist. Texture features were extracted using six properties calculated from gray-level co-occurrence matrices (GLCM), Minkowski Dimensions (MDs), and three Minkowski Functionals (MFs, e.g. MF.euler). A k-nearest-neighbor (k-NN) classifier and a Multilayer Radial Basis Functions Network (RBFN) were optimized in a 10-fold cross-validation for each texture vector, and the classification accuracy was calculated on independent test sets as a quantitative measure of automated tissue characterization. A Wilcoxon signed-rank test was used to compare two accuracy distributions and the significance thresholds were adjusted for multiple comparisons by the Bonferroni correction. The best classification results were obtained by the MF features, which performed significantly better than all the standard GLCM and MD features (p < 0.005) for both classifiers. The highest accuracy was found for MF.euler (97.5%, 96.6%; for the k-NN and RBFN classifier, respectively). The best standard texture features were the GLCM features 'homogeneity' (91.8%, 87.2%) and 'absolute value' (90.2%, 88.5%). The results indicate that advanced topological texture features can provide superior classification performance in computer-assisted diagnosis of interstitial lung diseases when compared to standard texture analysis methods.Comment: 8 pages, 5 figures, Proceedings SPIE Medical Imaging 201

    Classification of lung disease in HRCT scans using integral geometry measures and functional data analysis

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    A framework for classification of chronic lung disease from high-resolution CT scans is presented. We use a set of features which measure the local morphology and topology of the 3D voxels within the lung parenchyma and apply functional data classification to the extracted features. We introduce the measures, Minkowski functionals, which derive from integral geometry and show results of classification on lungs containing various stages of chronic lung disease: emphysema, fibrosis and honey-combing. Once trained, the presented method is shown to be efficient and specific at characterising the distribution of disease in HRCT slices

    Experimental and quantitative imaging techniques in interstitial lung disease.

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    Interstitial lung diseases (ILDs) are a heterogeneous group of conditions, with a wide and complex variety of imaging features. Difficulty in monitoring, treating and exploring novel therapies for these conditions is in part due to the lack of robust, readily available biomarkers. Radiological studies are vital in the assessment and follow-up of ILD, but currently CT analysis in clinical practice is qualitative and therefore somewhat subjective. In this article, we report on the role of novel and quantitative imaging techniques across a range of imaging modalities in ILD and consider how they may be applied in the assessment and understanding of ILD. We critically appraised evidence found from searches of Ovid online, PubMed and the TRIP database for novel and quantitative imaging studies in ILD. Recent studies have explored the capability of texture-based lung parenchymal analysis in accurately quantifying several ILD features. Newer techniques are helping to overcome the challenges inherent to such approaches, in particular distinguishing peripheral reticulation of lung parenchyma from pleura and accurately identifying the complex density patterns that accompany honeycombing. Robust and validated texture-based analysis may remove the subjectivity that is inherent to qualitative reporting and allow greater objective measurements of change over time. In addition to lung parenchymal feature quantification, pulmonary vessel volume analysis on CT has demonstrated prognostic value in two retrospective analyses and may be a sign of vascular changes in ILD which, to date, have been difficult to quantify in the absence of overt pulmonary hypertension. Novel applications of existing imaging techniques, such as hyperpolarised gas MRI and positron emission tomography (PET), show promise in combining structural and functional information. Although structural imaging of lung tissue is inherently challenging in terms of conventional proton MRI techniques, inroads are being made with ultrashort echo time, and dynamic contrast-enhanced MRI may be used for lung perfusion assessment. In addition, inhaled hyperpolarised 129Xenon gas MRI may provide multifunctional imaging metrics, including assessment of ventilation, intra-acinar gas diffusion and alveolar-capillary diffusion. PET has demonstrated high standard uptake values (SUVs) of 18F-fluorodeoxyglucose in fibrosed lung tissue, challenging the assumption that these are 'burned out' and metabolically inactive regions. Regions that appear structurally normal also appear to have higher SUV, warranting further exploration with future longitudinal studies to assess if this precedes future regions of macroscopic structural change. Given the subtleties involved in diagnosing, assessing and predicting future deterioration in many forms of ILD, multimodal quantitative lung structure-function imaging may provide the means of identifying novel, sensitive and clinically applicable imaging markers of disease. Such imaging metrics may provide mechanistic and phenotypic information that can help direct appropriate personalised therapy, can be used to predict outcomes and could potentially be more sensitive and specific than global pulmonary function testing. Quantitative assessment may objectively assess subtle change in character or extent of disease that can assist in efficacy of antifibrotic therapy or detecting early changes of potentially pneumotoxic drugs involved in early intervention studies

    CT-Based Local Distribution Metric Improves Characterization of COPD

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    Parametric response mapping (PRM) of paired CT lung images has been shown to improve the phenotyping of COPD by allowing for the visualization and quantification of non-emphysematous air trapping component, referred to as functional small airways disease (fSAD). Although promising, large variability in the standard method for analyzing PRM(fSAD) has been observed. We postulate that representing the 3D PRM(fSAD) data as a single scalar quantity (relative volume of PRM(fSAD)) oversimplifies the original 3D data, limiting its potential to detect the subtle progression of COPD as well as varying subtypes. In this study, we propose a new approach to analyze PRM. Based on topological techniques, we generate 3D maps of local topological features from 3D PRM(fSAD) classification maps. We found that the surface area of fSAD (S(fSAD)) was the most robust and significant independent indicator of clinically meaningful measures of COPD. We also confirmed by micro-CT of human lung specimens that structural differences are associated with unique S(fSAD) patterns, and demonstrated longitudinal feature alterations occurred with worsening pulmonary function independent of an increase in disease extent. These findings suggest that our technique captures additional COPD characteristics, which may provide important opportunities for improved diagnosis of COPD patients

    Infective/inflammatory disorders

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    The radiological investigation of musculoskeletal tumours : chairperson's introduction

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    Integrated Graph Theoretic, Radiomics, and Deep Learning Framework for Personalized Clinical Diagnosis, Prognosis, and Treatment Response Assessment of Body Tumors

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    Purpose: A new paradigm is beginning to emerge in radiology with the advent of increased computational capabilities and algorithms. The future of radiological reading rooms is heading towards a unique collaboration between computer scientists and radiologists. The goal of computational radiology is to probe the underlying tissue using advanced algorithms and imaging parameters and produce a personalized diagnosis that can be correlated to pathology. This thesis presents a complete computational radiology framework (I GRAD) for personalized clinical diagnosis, prognosis and treatment planning using an integration of graph theory, radiomics, and deep learning. Methods: There are three major components of the I GRAD framework–image segmentation, feature extraction, and clinical decision support. Image Segmentation: I developed the multiparametric deep learning (MPDL) tissue signature model for segmentation of normal and abnormal tissue from multiparametric (mp) radiological images. The segmentation MPDL network was constructed from stacked sparse autoencoders (SSAE) with five hidden layers. The MPDL network parameters were optimized using k-fold cross-validation. In addition, the MPDL segmentation network was tested on an independent dataset. Feature Extraction: I developed the radiomic feature mapping (RFM) and contribution scattergram (CSg) methods for characterization of spatial and inter-parametric relationships in multiparametric imaging datasets. The radiomic feature maps were created by filtering radiological images with first and second order statistical texture filters followed by the development of standardized features for radiological correlation to biology and clinical decision support. The contribution scattergram was constructed to visualize and understand the inter-parametric relationships of the breast MRI as a complex network. This multiparametric imaging complex network was modeled using manifold learning and evaluated using graph theoretic analysis. Feature Integration: The different clinical and radiological features extracted from multiparametric radiological images and clinical records were integrated using a hybrid multiview manifold learning technique termed the Informatics Radiomics Integration System (IRIS). IRIS uses hierarchical clustering in combination with manifold learning to visualize the high-dimensional patient space on a two-dimensional heatmap. The heatmap highlights the similarity and dissimilarity between different patients and variables. Results: All the algorithms and techniques presented in this dissertation were developed and validated using breast cancer as a model for diagnosis and prognosis using multiparametric breast magnetic resonance imaging (MRI). The deep learning MPDL method demonstrated excellent dice similarity of 0.87±0.05 and 0.84±0.07 for segmentation of lesions on malignant and benign breast patients, respectively. Furthermore, each of the methods, MPDL, RFM, and CSg demonstrated excellent results for breast cancer diagnosis with area under the receiver (AUC) operating characteristic (ROC) curve of 0.85, 0.91, and 0.87, respectively. Furthermore, IRIS classified patients with low risk of breast cancer recurrence from patients with medium and high risk with an AUC of 0.93 compared to OncotypeDX, a 21 gene assay for breast cancer recurrence. Conclusion: By integrating advanced computer science methods into the radiological setting, the I-GRAD framework presented in this thesis can be used to model radiological imaging data in combination with clinical and histopathological data and produce new tools for personalized diagnosis, prognosis or treatment planning by physicians

    Quantitative imaging in radiation oncology

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    Artificially intelligent eyes, built on machine and deep learning technologies, can empower our capability of analysing patients’ images. By revealing information invisible at our eyes, we can build decision aids that help our clinicians to provide more effective treatment, while reducing side effects. The power of these decision aids is to be based on patient tumour biologically unique properties, referred to as biomarkers. To fully translate this technology into the clinic we need to overcome barriers related to the reliability of image-derived biomarkers, trustiness in AI algorithms and privacy-related issues that hamper the validation of the biomarkers. This thesis developed methodologies to solve the presented issues, defining a road map for the responsible usage of quantitative imaging into the clinic as decision support system for better patient care

    Correlated Polarity Noise Reduction: Development, Analysis, and Application of a Novel Noise Reduction Paradigm

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    <p>Image noise is a pervasive problem in medical imaging. It is a property endemic to all imaging modalities and one especially familiar in those modalities that employ ionizing radiation. Statistical uncertainty is a major limiting factor in the reduction of ionizing radiation dose; patient exposure must be minimized but high image quality must also be achieved to retain the clinical utility of medical images. One way to achieve the goal of radiation dose reduction is through the use of image post processing with noise reduction algorithms. By acquiring images at lower than normal exposure followed by algorithmic noise reduction, it is possible to restore image noise to near normal levels. However, many denoising algorithms degrade the integrity of other image quality components in the process. </p><p>In this dissertation, a new noise reduction algorithm is investigated: Correlated Polarity Noise Reduction (CPNR). CPNR is a novel noise reduction technique that uses a statistical approach to reduce noise variance while maintaining excellent resolution and a "normal" noise appearance. In this work, the algorithm is developed in detail with the introduction of several methods for improving polarity estimation accuracy and maintaining the normality of the residual noise intensity distribution. Several image quality characteristics are assessed in the production of this new algorithm including its effects on residual noise texture, residual noise magnitude distribution, resolution effects, and nonlinear distortion effects. An in-depth review of current linear methods for medical imaging system resolution analysis will be presented along with several newly discovered improvements to existing techniques. This is followed by the presentation of a new paradigm for quantifying the frequency response and distortion properties of nonlinear algorithms. Finally, the new CPNR algorithm is applied to computed tomography (CT) to assess its efficacy as a dose reduction tool in 3-D imaging.</p><p>It was found that the CPNR algorithm can be used to reduce x ray dose in projection radiography by a factor of at least two without objectionable degradation of image resolution. This is comparable to other nonlinear image denoising algorithms such as the bilateral filter and wavelet denoising. However, CPNR can accomplish this level of dose reduction with few edge effects and negligible nonlinear distortion of the anatomical signal as evidenced by the newly developed nonlinear assessment paradigm. In application to multi-detector CT, XCAT simulations showed that CPNR can be used to reduce noise variance by 40% with minimal blurring of anatomical structures under a filtered back-projection reconstruction paradigm. When an apodization filter was applied, only 33% noise variance reduction was achieved, but the edge-saving qualities were largely retained. In application to cone-beam CT for daily patient positioning in radiation therapy, up to 49% noise variance reduction was achieved with as little as 1% reduction in the task transfer function measured from reconstructed data at the cutoff frequency. </p><p>This work concludes that the CPNR paradigm shows promise as a viable noise reduction tool which can be used to maintain current standards of clinical image quality at almost half of normal radiation exposure This algorithm has favorable resolution and nonlinear distortion properties as measured using a newly developed set of metrics for nonlinear algorithm resolution and distortion assessment. Simulation studies and the initial application of CPNR to cone-beam CT data reveal that CPNR may be used to reduce CT dose by 40%-49% with minimal degradation of image resolution.</p>Dissertatio
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