Perivascular Spaces Segmentation in Brain MRI Using Optimal 3D Filtering

Perivascular Spaces (PVS) are a recently recognised feature of Small Vessel Disease (SVD), also indicating neuroinflammation, and are an important part of the brain's circulation and glymphatic drainage system. Quantitative analysis of PVS on Magnetic Resonance Images (MRI) is important for understanding their relationship with neurological diseases. In this work, we propose a segmentation technique based on the 3D Frangi filtering for extraction of PVS from MRI. Based on prior knowledge from neuroradiological ratings of PVS, we used ordered logit models to optimise Frangi filter parameters in response to the variability in the scanner's parameters and study protocols. We optimized and validated our proposed models on two independent cohorts, a dementia sample (N=20) and patients who previously had mild to moderate stroke (N=48). Results demonstrate the robustness and generalisability of our segmentation method. Segmentation-based PVS burden estimates correlated with neuroradiological assessments (Spearman's $\rho$ = 0.74, p $<$ 0.001), suggesting the great potential of our proposed metho

Influence of threshold selection and image sequence in in-vivo segmentation of enlarged perivascular spaces

BACKGROUND: Growing interest surrounds perivascular spaces (PVS) as a clinical biomarker of brain dysfunction given their association with cerebrovascular risk factors and disease. Neuroimaging techniques allowing quick and reliable quantification are being developed, but, in practice, they require optimisation as their limits of validity are usually unspecified.NEW METHOD: We evaluate modifications and alternatives to a state-of-the-art (SOTA) PVS segmentation method that uses a vesselness filter to enhance PVS discrimination, followed by thresholding of its response, applied to brain magnetic resonance images (MRI) from patients with sporadic small vessel disease acquired at 3 T.RESULTS: The method is robust against inter-observer differences in threshold selection, but separate thresholds for each region of interest (i.e., basal ganglia, centrum semiovale, and midbrain) are required. Noise needs to be assessed prior to selecting these thresholds, as effect of noise and imaging artefacts can be mitigated with a careful optimisation of these thresholds. PVS segmentation from T1-weighted images alone, misses small PVS, therefore, underestimates PVS count, may overestimate individual PVS volume especially in the basal ganglia, and is susceptible to the inclusion of calcified vessels and mineral deposits. Visual analyses indicated the incomplete and fragmented detection of long and thin PVS as the primary cause of errors, with the Frangi filter coping better than the Jerman filter.COMPARISON WITH EXISTING METHODS: Limits of validity to a SOTA PVS segmentation method applied to 3 T MRI with confounding pathology are given.CONCLUSIONS: Evidence presented reinforces the STRIVE-2 recommendation of using T2-weighted images for PVS assessment wherever possible. The Frangi filter is recommended for PVS segmentation from MRI, offering robust output against variations in threshold selection and pathology presentation.</p

Extraction and quantification of perivascular spaces based on vesselness filtering: A potential biomarker for Fabry disease

Tese de mestrado integrado, Engenharia Biomédica e Biofísica (Engenharia Clínica e Instrumentação Médica), Universidade de Lisboa, Faculdade de Ciências, 2020Perivascular Spaces (PVS) allow interstitial solutes to be cleared from the brain contributing to the brain‘s homeostasis. Dysfunction of these pathways can occur if there is deposition of substances causing stagnation of fluid (CSF). Quantitative analysis of PVS on Magnetic Resonance Images (MRI) is important for understanding their relationship with dementia, stroke and vascular diseases. Manual delineation of PVS is very time consuming, and clinicians have to check multiple views in order to obtain a very accurate segmentation. Therefore, finding a method that would provide a reliable visual and quantitative information of a patient with PVS would enable a continuous monitoring giving clinical support throughout the development of each disease. Moreover, it would allow to understand and characterize PVS, provide useful insights into their role in normal brain physiology and small vessel disease (SVD). This work focused on the segmentation and further quantification of PVS in the brain using a vesselness filter (Frangi filter) . The Frangi filter, typically used to detect vessel-like or tube-like structures and fibers in volumetric image data, was capable to delineate, map and extract elongated and dot like features of PVS that were not easily seen when comparing with the non filtered images. However, this method requires a careful parameter optimization and further validation, since it presented different output behaviour in each MRI acquisition (T1-Weighted, T2-Weighted and T2-FLAIR). Also, quantitative analysis regarding the Frangi segmentation indicate that PVS visual rating scores may have a positive association with PVS volume. Statistical significance was found by clustering patients diagnosed with Multiple System atrophy (MSA), Progressive Supranuclear Palsy (PSP) and Fabry disease (FD) when compared with control patients

Enhancement of Perivascular Spaces in 7 T MR Image using Haar Transform of Non-local Cubes and Block-matching Filtering

Perivascular spaces (PVSs) in brain have a close relationship with typical neurological diseases. The quantitative studies of PVSs are meaningful but usually difficult, due to their thin and weak signals and also background noise in the 7 T brain magnetic resonance images (MRI). To clearly distinguish the PVSs in the 7 T MRI, we propose a novel PVS enhancement method based on the Haar transform of non-local cubes. Specifically, we extract a certain number of cubes from a small neighbor to form a cube group, and then perform Haar transform on each cube group. The Haar transform coefficients are processed using a nonlinear function to amplify the weak signals relevant to the PVSs and to suppress the noise. The enhanced image is reconstructed using the inverse Haar transform of the processed coefficients. Finally, we perform a block-matching 4D filtering on the enhanced image to further remove any remaining noise, and thus obtain an enhanced and denoised 7 T MRI for PVS segmentation. We apply two existing methods to complete PVS segmentation, i.e., (1) vesselness-thresholding and (2) random forest classification. The experimental results show that the PVS segmentation performances can be significantly improved by using the enhanced and denoised 7 T MRI

Application of the Ordered Logit Model to Optimising Frangi Filter Parameters for Segmentation of Perivascular Spaces

La segmentación de los espacios perivasculares (EVP) de las imágenes de resonancia magnética (RM) del cerebro es importante para comprender el sistema linfático del cerebro y su relación con las enfermedades neurológicas. El filtro Frangi podría ser una herramienta valiosa para este propósito. Sin embargo, sus parámetros deben ajustarse en respuesta a la variabilidad en los parámetros del escáner y los protocolos de estudio. Conociendo las clasificaciones neurorradiológicas del PVS, utilizamos el modelo logit ordenado para optimizar los parámetros del filtro Frangi. El volumen de PVS obtenido se correlacionó de manera significativa y fuerte con las evaluaciones neurorradiológicas (ρ = 0.75, p <0.001 de Spearman), lo que sugiere que el modelo logit ordenado podría ser una buena alternativa a los marcos de optimización convencionales para segmentar PVS en MRI

Rationale and design of a longitudinal study of cerebral small vessel diseases, clinical and imaging outcomes in patients presenting with mild ischaemic stroke: Mild Stroke Study 3

Background: Cerebral small vessel disease is a major cause of dementia and stroke, visible on brain magnetic resonance imaging. Recent data suggest that small vessel disease lesions may be dynamic, damage extends into normal-appearing brain and microvascular dysfunctions include abnormal blood–brain barrier leakage, vasoreactivity and pulsatility, but much remains unknown regarding underlying pathophysiology, symptoms, clinical features and risk factors of small vessel disease. Patients and Methods: The Mild Stroke Study 3 is a prospective observational cohort study to identify risk factors for and clinical implications of small vessel disease progression and regression among up to 300 adults with non-disabling stroke. We perform detailed serial clinical, cognitive, lifestyle, physiological, retinal and brain magnetic resonance imaging assessments over one year; we assess cerebrovascular reactivity, blood flow, pulsatility and blood–brain barrier leakage on magnetic resonance imaging at baseline; we follow up to four years by post and phone. The study is registered ISRCTN 12113543. Summary: Factors which influence direction and rate of change of small vessel disease lesions are poorly understood. We investigate the role of small vessel dysfunction using advanced serial neuroimaging in a deeply phenotyped cohort to increase understanding of the natural history of small vessel disease, identify those at highest risk of early disease progression or regression and uncover novel targets for small vessel disease prevention and therapy

Characterizing and revealing biomarkers on patients with Cerebral Amyloid Angiopathy using artificial intelligence

Dissertação de mestrado em BioinformáticaCerebral Amyloid Angiopathy is a cerebrovascular disorder resulting from the deposition of an amyloidogenic protein in small and medium sized cortical and leptomeningeal vessels. A primary cause of spontaneous intracerebral haemorrhages, it manifests predominantly in the elder population. Although CAA is a common neuropathological finding on itself, it is also known to frequently occur in conjunction with Alzheimer’s disease, being sometimes misdiagnosed. Currently, CAA diagnosis is generally conducted by post-mortem examination or, in live patients by the examination of an evacuated hematoma or brain biopsy samples, which are typically unavailable. Therefore, a reliable and non-invasive method for diagnosing CAA would facilitate the clinical decision making and accelerate the clinical intervention. The main goal of this dissertation is to study the application of Machine Learning (ML) to reveal possible biomarkers to aid the diagnosis and early medical intervention, and better understand the disease. Therefore, three scenarios were tested: Classification of four neurodegenerative diseases with annotation data obtained from visual rating scores, age and gender; Classification of the diseases with radiomic data derived from the patient’s MRI; and a combination of the previous experiments. The results show that the application of Artificial intelligence in the medical field brings advantages to support the physicians in the decision making process and, at some point, make a correct prediction of the disease label. Although the results are satisfactory, there are still improvements to be done. For instance, image segmentation of cerebral lesions or brain regions and additional clinical information of the patients would be of value.Angiopatia Amiloide Cerebral (AAC) é uma doença vascular cerebral resultante da deposição de matéria amiloide. Principal causa de hemorragias cerebral espontâneas, a AAC manifesta se predominantemente na população idosa. Embora a AAC seja uma doença que por si só tem um grande impacto no grupo etário referido, ocorre em simultâneo com inúmeras outras doenças neurodegenerativas, como a doença de Alzheimer. Atualmente, o diagnóstico de AAC realiza-se quer em post-mortem, quer em pacientes vivos. No entanto, o diagnóstico em vida é conseguido por meio de biópsias de tecidos cerebrais, sendo um método invasivo, o que dificulta a intervenção clínica. Deste modo, torna-se imperativa a procura de alternativas fiáveis e não invasivas em vida para auxiliar o diagnóstico da doença e permitir a melhoria da qualidade de vida do paciente. Perante os progressos na área da tecnologia e medicina, esta dissertação propõe o estudo da aplicação de algoritmos de Machine Learning (ML) para revelar possíveis biomarcadores para auxiliar o diagnóstico e permitir uma intervenção precoce. Deste modo, foram testados três cenários distintos: a classificação de quatro doenças neurodegenerativas com dados anotados obtidos a partir de métricas visuais de avaliação da atrofia, idade e sexo; a classificação das doenças com dados gerados a partir de métodos radiómicos; e uma combinação das duas abordagens anteriores. Neste documento apresenta-se e discute-se os resultados obtidos com a aplicação de quatro diferentes algoritmos de ML que visam a deteção automática da doença associada à imagem testada. Adicionalmente, é feita uma análise crítica de quais as características mais relevantes que levaram à tomada de decisão por parte do algoritmo. Os resultados demonstram que através de aplicação de metodologias automáticas é possível o auxílio ao diagnostico médico por especialistas e, no limite, a realização de diagnostico automático com elevada precisão. Finalmente, são apresentadas possíveis alternativas de trabalho futuro para que os resultados possam ser aperfeiçoados, como por exemplo, a segmentação das regiões de interesse, i.e., identificação das lesões, aquando da anotação por especialistas. Mediante a inclusão dessa segmentação, uma vez que será mais especifica, os resultados serão, por sua vez, aprimorados

Segmentation of perivascular spaces in 7 T MR image using auto-context model with orientation-normalized features

Quantitative study of perivascular spaces (PVSs) in brain magnetic resonance (MR) images is important for understanding the brain lymphatic system and its relationship with neurological diseases. One of major challenges is the accurate extraction of PVSs that have very thin tubular structures with various directions in three-dimensional (3D) MR images. In this paper, we propose a learning-based PVS segmentation method to address this challenge. Specifically, we first determine a region of interest (ROI) by using the anatomical brain structure and the vesselness information derived from eigenvalues of image derivatives. Then, in the ROI, we extract a number of randomized Haar features which are normalized with respect to the principal directions of the underlying image derivatives. The classifier is trained by the random forest model that can effectively learn both discriminative features and classifier parameters to maximize the information gain. Finally, a sequential learning strategy is used to further enforce various contextual patterns around the thin tubular structures into the classifier. For evaluation, we apply our proposed method to the 7T brain MR images scanned from 17 healthy subjects aged from 25 to 37. The performance is measured by voxel-wise segmentation accuracy, cluster- wise classification accuracy, and similarity of geometric properties, such as volume, length, and diameter distributions between the predicted and the true PVSs. Moreover, the accuracies are also evaluated on the simulation images with motion artifacts and lacunes to demonstrate the potential of our method in segmenting PVSs from elderly and patient populations. The experimental results show that our proposed method outperforms all existing PVS segmentation methods

Topological relationships between perivascular spaces and progression of white matter hyperintensities:A pilot study in a sample of the Lothian Birth Cohort 1936

Enlarged perivascular spaces (PVS) and white matter hyperintensities (WMH) are features of cerebral small vessel disease which can be seen in brain magnetic resonance imaging (MRI). Given the associations and proposed mechanistic link between PVS and WMH, they are hypothesized to also have topological proximity. However, this and the influence of their spatial proximity on WMH progression are unknown. We analyzed longitudinal MRI data from 29 out of 32 participants (mean age at baseline = 71.9 years) in a longitudinal study of cognitive aging, from three waves of data collection at 3-year intervals, alongside semi-automatic segmentation masks for PVS and WMH, to assess relationships. The majority of deep WMH clusters were found adjacent to or enclosing PVS (waves−1: 77%; 2: 76%; 3: 69%), especially in frontal, parietal, and temporal regions. Of the WMH clusters in the deep white matter that increased between waves, most increased around PVS (waves−1–2: 73%; 2–3: 72%). Formal statistical comparisons of severity of each of these two SVD markers yielded no associations between deep WMH progression and PVS proximity. These findings may suggest some deep WMH clusters may form and grow around PVS, possibly reflecting the consequences of impaired interstitial fluid drainage via PVS. The utility of these relationships as predictors of WMH progression remains unclear