456 research outputs found
Multiple Sclerosis Detection in Multispectral Magnetic Resonance Images with Principal Components Analysis
This paper presents a local feature vector based method for automated Multiple Sclerosis (MS) lesion segmentation of multi spectral MRI data. Twenty datasets from MS patients with FLAIR, T1,T2, MD and FA data with expert annotations are available as training set from the MICCAI 2008 challenge on MS, and 24 test datasets. Our local feature vector method contains neighbourhood voxel intensities, histogram and MS probability atlas information. Principal Component Analysis(PCA) with log-likelihood ratio is used to classify each voxel. MRI suffers from intensity inhomogenities. We try to correct this 'bias field' with 3 methods: a genetic algorithm, edge preserving filtering and atlas based correction. A large observer variability exist between expert classifications, but the similarity scores between model and expert classifications are often lower. Our model gives the best classification results with raw data, because bias correction gives artifacts at the edges and flatten large MS lesions
Deteção automática de lesões de esclerose múltipla em imagens de ressonância magnética cerebral utilizando BIANCA
The aim of this work was to design and optimize a workflow to apply the
Machine Learning classifier BIANCA (Brain Intensity AbNormalities
Classification Algorithm) to detect lesions characterized by white matter T2
hyperintensity in clinical Magnetic Resonance Multiple Sclerosis datasets.
The designed pipeline includes pre-processing, lesion identification and
optimization of BIANCA options.
The classifier has been trained and tuned on 15 cases making up the training
dataset of the MICCAI 2016 (Medical Image Computing and Computer
Assisted Interventions) challenge and then tested on 30 cases from the Lesjak
et al. public dataset.
The results obtained are in good agreement with those reported by the 13
teams concluding the MICCAI 2016 challenge, thus confirming that this
algorithm can be a reliable tool to detect and classify Multiple Sclerosis lesions
in Magnetic Resonance studies.Este trabalho teve como objetivo a conceção e otimização de um procedimento
para aplicação de um algoritmo de Machine Learning, o classificador BIANCA
(Brain Intensity AbNormalities Classification Algorithm), para deteção de lesões
caracterizadas por hiperintensidade em T2 da matéria branca em estudos
clÃnicos de Esclerose Múltipla por Ressonância Magnética.
O procedimento concebido inclui pré-processamento, identificação das lesões
e otimização dos parâmetros do algoritmo BIANCA.
O classificador foi treinado e afinado utilizando os 15 casos clÃnicos que
constituÃam o conjunto de treino do desafio MICCAI 2016 (Medical Image
Computing and Computer Assisted Interventions) e posteriormente testado em
30 casos clÃnicos de uma base de dados pública (Lesjak et al.).
Os resultados obtidos são em concordância com os alcançados pelas 13
equipas que concluÃram o desafio MICCAI 2016, confirmando que este
algoritmo pode ser uma ferramenta válida para a deteção e classificação de
lesões de Esclerose Múltipla em estudos de Ressonância Magnética.Mestrado em Tecnologias da Imagem Médic
Neuroimaging of structural pathology and connectomics in traumatic brain injury: Toward personalized outcome prediction.
Recent contributions to the body of knowledge on traumatic brain injury (TBI) favor the view that multimodal neuroimaging using structural and functional magnetic resonance imaging (MRI and fMRI, respectively) as well as diffusion tensor imaging (DTI) has excellent potential to identify novel biomarkers and predictors of TBI outcome. This is particularly the case when such methods are appropriately combined with volumetric/morphometric analysis of brain structures and with the exploration of TBI-related changes in brain network properties at the level of the connectome. In this context, our present review summarizes recent developments on the roles of these two techniques in the search for novel structural neuroimaging biomarkers that have TBI outcome prognostication value. The themes being explored cover notable trends in this area of research, including (1) the role of advanced MRI processing methods in the analysis of structural pathology, (2) the use of brain connectomics and network analysis to identify outcome biomarkers, and (3) the application of multivariate statistics to predict outcome using neuroimaging metrics. The goal of the review is to draw the community's attention to these recent advances on TBI outcome prediction methods and to encourage the development of new methodologies whereby structural neuroimaging can be used to identify biomarkers of TBI outcome
Exploring variability in medical imaging
Although recent successes of deep learning and novel machine learning techniques improved the perfor-
mance of classification and (anomaly) detection in computer vision problems, the application of these
methods in medical imaging pipeline remains a very challenging task. One of the main reasons for this
is the amount of variability that is encountered and encapsulated in human anatomy and subsequently
reflected in medical images. This fundamental factor impacts most stages in modern medical imaging
processing pipelines.
Variability of human anatomy makes it virtually impossible to build large datasets for each disease
with labels and annotation for fully supervised machine learning. An efficient way to cope with this is
to try and learn only from normal samples. Such data is much easier to collect. A case study of such
an automatic anomaly detection system based on normative learning is presented in this work. We
present a framework for detecting fetal cardiac anomalies during ultrasound screening using generative
models, which are trained only utilising normal/healthy subjects.
However, despite the significant improvement in automatic abnormality detection systems, clinical
routine continues to rely exclusively on the contribution of overburdened medical experts to diagnosis
and localise abnormalities. Integrating human expert knowledge into the medical imaging processing
pipeline entails uncertainty which is mainly correlated with inter-observer variability. From the per-
spective of building an automated medical imaging system, it is still an open issue, to what extent
this kind of variability and the resulting uncertainty are introduced during the training of a model
and how it affects the final performance of the task. Consequently, it is very important to explore the
effect of inter-observer variability both, on the reliable estimation of model’s uncertainty, as well as
on the model’s performance in a specific machine learning task. A thorough investigation of this issue
is presented in this work by leveraging automated estimates for machine learning model uncertainty,
inter-observer variability and segmentation task performance in lung CT scan images.
Finally, a presentation of an overview of the existing anomaly detection methods in medical imaging
was attempted. This state-of-the-art survey includes both conventional pattern recognition methods
and deep learning based methods. It is one of the first literature surveys attempted in the specific
research area.Open Acces
Slowly expanding lesions relate to persisting black-holes and clinical outcomes in relapse-onset multiple sclerosis
Black holes; Chronic active lesions; Volumetric MRIAgujeros negros; Lesiones activas crónicas; Resonancia magnética volumétricaForats negres; Lesions actives cròniques; Ressonà ncia magnètica volumètricaBackground
Slowly expanding lesions (SELs) are MRI markers of chronic active lesions in multiple sclerosis (MS). T1-hypointense black holes, and reductions in magnetization transfer ratio (MTR) are pathologically correlated with myelin and axonal loss. While all associated with progressive MS, the relationship between these lesion’s metrics and clinical outcomes in relapse-onset MS has not been widely investigated.
Objectives
To explore the relationship of SELs with T1-hypointense black holes, and longitudinal T1 intensity contrast ratio and MTR, their correlation to brain volume, and their contribution to MS disability in relapse-onset patients.
Methods
135 patients with relapsing-remitting MS (RRMS) were studied with clinical assessments and brain MRI (T2/FLAIR and T1-weighted scans at 1.5/3 T) at baseline and two subsequent follow-ups; a subset of 83 patients also had MTR acquisitions. Early-onset patients were defined when the baseline disease duration was ≤ 5 years (n = 85). SELs were identified using deformation field maps from the manually segmented baseline T2 lesions and differentiated from the non-SELs. Persisting black holes (PBHs) were defined as a subset of T2 lesions with a signal below a patient-specific grey matter T1 intensity in a semi-quantitative manner. SELs, PBH counts, and brain volume were computed, and their associations were assessed through Spearman and Pearson correlation. Clusters of patients according to low (up to 2), intermediate (3 to 10), or high (more than 10) SEL counts were determined with a Gaussian generalised mixture model. Mixed-effects and logistic regression models assessed volumes, T1 and MTR within SELs, and their correlation with Expanded Disability Status Scale (EDSS) and confirmed disability progression (CDP).
Results
Mean age at study onset was 35.5 years (73% female), disease duration 5.5 years and mean time to last follow-up 6.5 years (range 1 to 12.5); median baseline EDSS 1.5 (range 0 to 5.5) and a mean EDSS change of 0.31 units at final follow-up. Among 4007 T2 lesions, 27% were classified as SELs and 10% as PBHs. Most patients (n = 65) belonged to the cluster with an intermediate SEL count (3 to 10 SELs). The percentage of PBHs was higher in SELs than non-SELs (up to 61% vs 44%, p < 0.001) and within-patient SEL volumes positively correlated with PBH volumes (r = 0.53, p < 0.001). SELs showed a decrease in T1 intensity over time (beta = -0.004, 95%CI −0.005 to −0.003, p < 0.001), accompanied by lower cross-sectional baseline and follow-up MTR. In mixed-effects models, EDSS worsening was predicted by the SEL log-volumes increase over time (beta = 0.11, 95%CI 0.03 to 0.20, p = 0.01), which was confirmed in the sub-cohort of patients with early onset MS (beta = 0.14, 95%CI 0.04 to 0.25, p = 0.008). In logistic regressions, a higher risk for CDP was associated with SEL volumes (OR = 5.15, 95%CI 1.60 to 16.60, p = 0.006).
Conclusions
SELs are associated with accumulation of more destructive pathology as indicated by an association with PBH volume, longitudinal reduction in T1 intensity and MTR. Higher SEL volumes are associated with clinical progression, while lower ones are associated with stability in relapse-onset MS
A Survey on Deep Learning in Medical Image Analysis
Deep learning algorithms, in particular convolutional networks, have rapidly
become a methodology of choice for analyzing medical images. This paper reviews
the major deep learning concepts pertinent to medical image analysis and
summarizes over 300 contributions to the field, most of which appeared in the
last year. We survey the use of deep learning for image classification, object
detection, segmentation, registration, and other tasks and provide concise
overviews of studies per application area. Open challenges and directions for
future research are discussed.Comment: Revised survey includes expanded discussion section and reworked
introductory section on common deep architectures. Added missed papers from
before Feb 1st 201
Slowly expanding lesions relate to persisting black-holes and clinical outcomes in relapse-onset multiple sclerosis
Background: Slowly expanding lesions (SELs) are MRI markers of chronic active lesions in multiple sclerosis (MS). T1-hypointense black holes, and reductions in magnetization transfer ratio (MTR) are pathologically correlated with myelin and axonal loss. While all associated with progressive MS, the relationship between these lesion's metrics and clinical outcomes in relapse-onset MS has not been widely investigated. Objectives: To explore the relationship of SELs with T1-hypointense black holes, and longitudinal T1 intensity contrast ratio and MTR, their correlation to brain volume, and their contribution to MS disability in relapse-onset patients. Methods: 135 patients with relapsing-remitting MS (RRMS) were studied with clinical assessments and brain MRI (T2/FLAIR and T1-weighted scans at 1.5/3 T) at baseline and two subsequent follow-ups; a subset of 83 patients also had MTR acquisitions. Early-onset patients were defined when the baseline disease duration was & LE; 5 years (n = 85). SELs were identified using deformation field maps from the manually segmented baseline T2 lesions and differentiated from the non-SELs. Persisting black holes (PBHs) were defined as a subset of T2 lesions with a signal below a patient-specific grey matter T1 intensity in a semi-quantitative manner. SELs, PBH counts, and brain volume were computed, and their associations were assessed through Spearman and Pearson correlation. Clusters of patients according to low (up to 2), intermediate (3 to 10), or high (more than 10) SEL counts were determined with a Gaussian generalised mixture model. Mixed-effects and logistic regression models assessed volumes, T1 and MTR within SELs, and their correlation with Expanded Disability Status Scale (EDSS) and confirmed disability progression (CDP). Results: Mean age at study onset was 35.5 years (73% female), disease duration 5.5 years and mean time to last follow-up 6.5 years (range 1 to 12.5); median baseline EDSS 1.5 (range 0 to 5.5) and a mean EDSS change of 0.31 units at final follow-up. Among 4007 T2 lesions, 27% were classified as SELs and 10% as PBHs. Most patients (n = 65) belonged to the cluster with an intermediate SEL count (3 to 10 SELs). The percentage of PBHs was higher in SELs than non-SELs (up to 61% vs 44%, p < 0.001) and within-patient SEL volumes positively correlated with PBH volumes (r = 0.53, p < 0.001). SELs showed a decrease in T1 intensity over time (beta = -0.004, 95%CI -0.005 to -0.003, p < 0.001), accompanied by lower cross-sectional baseline and follow-up MTR. In mixed effects models, EDSS worsening was predicted by the SEL log-volumes increase over time (beta = 0.11, 95% CI 0.03 to 0.20, p = 0.01), which was confirmed in the sub-cohort of patients with early onset MS (beta = 0.14, 95%CI 0.04 to 0.25, p = 0.008). In logistic regressions, a higher risk for CDP was associated with SEL volumes (OR = 5.15, 95%CI 1.60 to 16.60, p = 0.006). Conclusions: SELs are associated with accumulation of more destructive pathology as indicated by an association with PBH volume, longitudinal reduction in T1 intensity , MTR. Higher SEL volumes are associated with clinical progression, while lower ones are associated with stability in relapse-onset MS
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