Oualid M. Benkarim
Pompeu Fabra University
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Featured researches published by Oualid M. Benkarim.
International Workshop on Machine Learning in Medical Imaging | 2016
Gerard Sanroma; Oualid M. Benkarim; Gemma Piella; Miguel Ángel González Ballester
Two common ways of approaching atlas-based segmentation of brain MRI are (1) intensity-based modelling and (2) multi-atlas label fusion. Intensity-based methods are robust to registration errors but need distinctive image appearances. Multi-atlas label fusion can identify anatomical correspondences with faint appearance cues, but needs a reasonable registration. We propose an ensemble segmentation method that combines the complementary features of both types of approaches. Our method uses the probabilistic estimates of the base methods to compute their optimal combination weights in a spatially varying way. We also propose an intensity-based method (to be used as base method) that offers a trade-off between invariance to registration errors and dependence on distinct appearances. Results show that sacrificing invariance to registration errors (up to a certain degree) improves the performance of our intensity-based method. Our proposed ensemble method outperforms the rest of participating methods in most of the structures of the NeoBrainS12 Challenge on neonatal brain segmentation. We achieve up to \(\sim \)10 % of improvement in some structures.
Human Brain Mapping | 2017
Oualid M. Benkarim; Gerard Sanroma; Veronika A. M. Zimmer; Emma Muñoz-Moreno; N.M. Hahner; Elisenda Eixarch; Oscar Camara; Miguel Ángel González Ballester; Gemma Piella
Investigating the human brain in utero is important for researchers and clinicians seeking to understand early neurodevelopmental processes. With the advent of fast magnetic resonance imaging (MRI) techniques and the development of motion correction algorithms to obtain high‐quality 3D images of the fetal brain, it is now possible to gain more insight into the ongoing maturational processes in the brain. In this article, we present a review of the major building blocks of the pipeline toward performing quantitative analysis of in vivo MRI of the developing brain and its potential applications in clinical settings. The review focuses on T1‐ and T2‐weighted modalities, and covers state of the art methodologies involved in each step of the pipeline, in particular, 3D volume reconstruction, spatio‐temporal modeling of the developing brain, segmentation, quantification techniques, and clinical applications. Hum Brain Mapp 38:2772–2787, 2017.
medical image computing and computer assisted intervention | 2016
Oualid M. Benkarim; Gemma Piella; Miguel Ángel González Ballester; Gerard Sanroma
Multiple-atlas segmentation has recently shown success in automatic segmentation of brain images. It consists in registering the labelmaps from a set of atlases to the anatomy of a target image, and then fusing the multiple labelmaps into a consensus segmentation on the target image. Accurately estimating the confidence of each atlas decision is key for the success of label fusion. Common approaches either rely on local patch similarity, probabilistic statistical frameworks or a combination of both. We present a probabilistic label fusion framework that takes into account label confidence at each point. Maximum likelihood atlas confidences are estimated by explicitly modelling the relationship between image appearance and segmentation errors. We also propose a novel type of label-dependent appearance features based on atlas labelmaps. Our results indicate that the proposed label fusion framework achieves state-of-the-art performance in the segmentation of subcortical structures.
international conference on machine learning | 2015
Gerard Sanroma; Oualid M. Benkarim; Gemma Piella; Guorong Wu; Xiaofeng Zhu; Dinggang Shen; Miguel Ángel González Ballester
In this last decade, multiple-atlas segmentation MAS has emerged as a promising technique for medical image segmentation. In MAS, a novel target image is segmented by fusing the label maps of a set of annotated images or atlases, after spatial normalization. Weighted voting is a well-known label fusion strategy consisting of computing each target label as a weighted average of the atlas labels in a local neighborhood. The weights, denoting the local anatomical similarity of the candidate atlases, are often approximated using image-patch similarity measurements. Such an approach, known as patch-based label fusion PBLF, may fail to discriminate the anatomically relevant patches in challenging regions with high label variability. In order to overcome this limitation we propose a supervised method that embeds the original image patches onto a space that emphasizes the appearance characteristics that are critical for a correct labeling, while supressing the irrelevant ones. We show that PBLF using the embedded patches compares favourably with state-of-the-art methods in brain MR image segmentation experiments.
NeuroImage: Clinical | 2018
Oualid M. Benkarim; Nadine Hahner; Gemma Piella; Eduard Gratacós; Miguel Ángel González Ballester; Elisenda Eixarch; Gerard Sanroma
Neuroimaging of brain diseases plays a crucial role in understanding brain abnormalities and early diagnosis. Of great importance is the study of brain abnormalities in utero and the assessment of deviations in case of maldevelopment. In this work, brain magnetic resonance images from 23 isolated non-severe ventriculomegaly (INSVM) fetuses and 25 healthy controls between 26 and 29 gestational weeks were used to identify INSVM-related cortical folding deviations from normative development. Since these alterations may reflect abnormal neurodevelopment, our working hypothesis is that markers of cortical folding can provide cues to improve the prediction of later neurodevelopmental problems in INSVM subjects. We analyzed the relationship of ventricular enlargement with cortical folding alterations in a regional basis using several curvature-based measures describing the folding of each cortical region. Statistical analysis (global and hemispheric) and sparse linear regression approaches were then used to find the cortical regions whose folding is associated with ventricular dilation. Results from both approaches were in great accordance, showing a significant cortical folding decrease in the insula, posterior part of the temporal lobe and occipital lobe. Moreover, compared to the global analysis, stronger ipsilateral associations of ventricular enlargement with reduced cortical folding were encountered by the hemispheric analysis. Our findings confirm and extend previous studies by identifying various cortical regions and emphasizing ipsilateral effects of ventricular enlargement in altered folding. This suggests that INSVM is an indicator of altered cortical development, and moreover, cortical regions with reduced folding constitute potential prognostic biomarkers to be used in follow-up studies to decipher the outcome of INSVM fetuses.
International Workshop on Patch-based Techniques in Medical Imaging | 2017
Gerard Sanroma; Víctor Andrea; Oualid M. Benkarim; José V. Manjón; Pierrick Coupé; Oscar Camara; Gemma Piella; Miguel Ángel González Ballester
Alzheimer’s disease (AD) is characterized by a progressive decline in the cognitive functions accompanied by an atrophic process which can already be observed in the early stages using magnetic resonance images (MRI). Individualized prediction of future progression to AD, when patients are still in the mild cognitive impairment (MCI) stage, has potential impact for preventive treatment. Atrophy patterns extracted from longitudinal MRI sequences provide valuable information to identify MCI patients at higher risk of developing AD in the future. We present a novel descriptor that uses the similarity between local image patches to encode local displacements due to atrophy between a pair of longitudinal MRI scans. Using a conventional logistic regression classifier, our descriptor achieves \(76\%\) accuracy in predicting which MCI patients will progress to AD up to 3 years before conversion.
medical image computing and computer assisted intervention | 2018
Oualid M. Benkarim; Gerard Sanroma; Gemma Piella; Islem Rekik; Nadine Hahner; Elisenda Eixarch; Miguel Ángel González Ballester; Dinggang Shen; Gang Li
Fetal ventriculomegaly (VM) is a condition with dilation of one or both lateral ventricles, and is diagnosed as an atrial diameter larger than 10 mm. Evidence of altered cortical folding associated with VM has been shown in the literature. However, existing studies use a holistic approach (i.e., ventricle as a whole) based on diagnosis or ventricular volume, thus failing to reveal the spatially-heterogeneous association patterns between cortex and ventricle. To address this issue, we develop a novel method to identify spatially fine-scaled association maps between cortical development and VM by leveraging vertex-wise correlations between the growth patterns of both ventricular and cortical surfaces in terms of area expansion and curvature information. Our approach comprises multiple steps. In the first step, we define a joint graph Laplacian matrix using cortex-to-ventricle correlations. Next, we propose a spectral embedding of the cortex-to-ventricle graph into a common underlying space where their joint growth patterns are projected. More importantly, in the joint ventricle-cortex space, the vertices of associated regions from both cortical and ventricular surfaces would lie close to each other. In the final step, we perform clustering in the joint embedded space to identify associated sub-regions between cortex and ventricle. Using a dataset of 25 healthy fetuses and 23 fetuses with isolated non-severe VM within the age range of 26-29 gestational weeks, our results show that the proposed approach is able to reveal clinically relevant and meaningful regional associations.
Medical Image Analysis | 2018
Gerard Sanroma; Oualid M. Benkarim; Gemma Piella; Oscar Camara; Guorong Wu; Dinggang Shen; Juan Domingo Gispert; José Luis Molinuevo; Miguel Ángel González Ballester; Alzheimer's Disease Neuroimaging Initiative
HighlightsWe present a method to improve discriminative abilities of patch‐based label fusion.We use neural networks to learn optimal embeddings of image patches.Our method allows for embeddings with different complexities.Our method scales linearly with the number of atlases both in train and test phases.Results show an improvement over standard PBLF even with the simplest embeddings. Graphical abstract Figure. No Caption available. Abstract In brain structural segmentation, multi‐atlas strategies are increasingly being used over single‐atlas strategies because of their ability to fit a wider anatomical variability. Patch‐based label fusion (PBLF) is a type of such multi‐atlas approaches that labels each target point as a weighted combination of neighboring atlas labels, where atlas points with higher local similarity to the target contribute more strongly to label fusion. PBLF can be potentially improved by increasing the discriminative capabilities of the local image similarity measurements. We propose a framework to compute patch embeddings using neural networks so as to increase discriminative abilities of similarity‐based weighted voting in PBLF. As particular cases, our framework includes embeddings with different complexities, namely, a simple scaling, an affine transformation, and non‐linear transformations. We compare our method with state‐of‐the‐art alternatives in whole hippocampus and hippocampal subfields segmentation experiments using publicly available datasets. Results show that even the simplest versions of our method outperform standard PBLF, thus evidencing the benefits of discriminative learning. More complex transformation models tended to achieve better results than simpler ones, obtaining a considerable increase in average Dice score compared to standard PBLF.
Computerized Medical Imaging and Graphics | 2018
Gerard Sanroma; Oualid M. Benkarim; Gemma Piella; Karim Lekadir; N.M. Hahner; Elisenda Eixarch; Miguel Ángel González Ballester
Segmentation of brain structures during the pre-natal and early post-natal periods is the first step for subsequent analysis of brain development. Segmentation techniques can be roughly divided into two families. The first, which we denote as registration-based techniques, rely on initial estimates derived by registration to one (or several) templates. The second family, denoted as learning-based techniques, relate imaging (and spatial) features to their corresponding anatomical labels. Each approach has its own qualities and both are complementary to each other. In this paper, we explore two ensembling strategies, namely, stacking and cascading to combine the strengths of both families. We present experiments on segmentation of 6-month infant brains and a cohort of fetuses with isolated non-severe ventriculomegaly (INSVM). INSVM is diagnosed when ventricles are mildly enlarged and no other anomalies are apparent. Prognosis is difficult based solely on the degree of ventricular enlargement. In order to find markers for a more reliable prognosis, we use the resulting segmentations to find abnormalities in the cortical folding of INSVM fetuses. Segmentation results show that either combination strategy outperform all of the individual methods, thus demonstrating the capability of learning systematic combinations that lead to an overall improvement. In particular, the cascading strategy outperforms the ensembling one, the former one obtaining top 5, 7 and 13 results (out of 21 teams) in the segmentation of white matter, gray matter and cerebro-spinal fluid in the iSeg2017 MICCAI Segmentation Challenge. The resulting segmentations reveal that INSVM fetuses have a less convoluted cortex. This points to cortical folding abnormalities as potential markers of later neurodevelopmental outcomes.
Medical Image Analysis | 2017
Oualid M. Benkarim; Gemma Piella; Miguel Ángel González Ballester; Gerard Sanroma
HighlightsWe propose a probabilistic label fusion approach for multi‐atlas segmentation.Discriminative learning is used to learn from atlas segmentation errors.We explore different spatial pooling strategies for modeling such errors.Novel label‐dependent features are proposed to augment our feature vectors.Results on brain MRI segmentation show state‐of‐the‐art performance. Graphical abstract Figure. No caption available. ABSTRACT Quantitative neuroimaging analyses often rely on the accurate segmentation of anatomical brain structures. In contrast to manual segmentation, automatic methods offer reproducible outputs and provide scalability to study large databases. Among existing approaches, multi‐atlas segmentation has recently shown to yield state‐of‐the‐art performance in automatic segmentation of brain images. It consists in propagating the labelmaps from a set of atlases to the anatomy of a target image using image registration, and then fusing these multiple warped labelmaps into a consensus segmentation on the target image. Accurately estimating the contribution of each atlas labelmap to the final segmentation is a critical step for the success of multi‐atlas segmentation. Common approaches to label fusion either rely on local patch similarity, probabilistic statistical frameworks or a combination of both. In this work, we propose a probabilistic label fusion framework based on atlas label confidences computed at each voxel of the structure of interest. Maximum likelihood atlas confidences are estimated using a supervised approach, explicitly modeling the relationship between local image appearances and segmentation errors produced by each of the atlases. We evaluate different spatial pooling strategies for modeling local segmentation errors. We also present a novel type of label‐dependent appearance features based on atlas labelmaps that are used during confidence estimation to increase the accuracy of our label fusion. Our approach is evaluated on the segmentation of seven subcortical brain structures from the MICCAI 2013 SATA Challenge dataset and the hippocampi from the ADNI dataset. Overall, our results indicate that the proposed label fusion framework achieves superior performance to state‐of‐the‐art approaches in the majority of the evaluated brain structures and shows more robustness to registration errors.