Abstract:The hippocampus is one of the first brain structures affected by Alzheimer's disease (AD). While many automatic methods for hippocampal segmentation exist, few studies have compared them on the same data. In this study, we compare four fully automated hippocampal segmentation methods in terms of their conformity with manual segmentation and their ability to be used as an AD biomarker in clinical settings. We also apply error correction to the four automatic segmentation methods, and complete a comprehensive va… Show more
“…Twenty subjects were selected from each of the following clinical subgroups: normal controls, mild cognitive impairment, and Alzheimer's disease. Since this dataset was previously used to compare several state‐of‐the‐art algorithms (Zandifar et al, ), for our experiments, we use the same data (e.g., previously preprocessed as described in Zandifar et al) to enable meaningful comparisons with the results reported in the aforementioned work. Pre‐processing consisted of patch‐based (PB) denoising (Coupé et al, ), N3 nonuniformity correction (Sled, Zijdenbos, & Evans, ), linear intensity normalization to the range [0,100], and affine registration to the MNI‐ICBM152 template (Fonov et al, ) with 1 × 1 × 1 mm 3 resolution.…”
Section: Experiments and Resultsmentioning
confidence: 99%
“…We further compared several variants of our CNN‐based method with several other popular and/or state‐of‐the‐art segmentation methods on the same dataset using the segmentations previously produced in the work of Zandifar et al (), which includes results for four different methods, both before and after applying EC (Wang et al, ), a machine learning based wrapper which attempts to correct systematic errors made by the initial host segmentation method. The methods included are FreeSurfer (Fischl, ), ANIMAL (Collins & Pruessner, ) (a multiatlas technique combining nonlinear registration with majority‐vote label fusion), traditional PB segmentation (Coupé et al, ) (a multiatlas technique combining linear registration with PB label fusion), and an augmented approach combining PB segmentation with nonlinear registration.…”
Section: Experiments and Resultsmentioning
confidence: 99%
“…Note that the results from the 2.5D CNN method (Kushibar et al, 2018) are not included in the boxplots because only summary statistics were available. Of our CNN-based methods, the performance of the baseline network CNN-B was poorest overall T A B L E 5 Comparison of four of our CNN-based segmentation methods with previously reported results (Zandifar et al, 2017)…”
Section: Subcortical Segmentation In the Ibsr Datasetmentioning
confidence: 89%
“…Some such methods have attempted to learn complex mappings between image features and labels using traditional machine-learning based classifiers (e.g., support vector machines (Boser, Guyon, & Vapnik, 1992) and random forests (Breiman, 2001)) combined with handcrafted feature sets (Morra et al, 2010;Zikic et al, 2012), while others have found success transferring labels using a combination of linear or nonlinear image registration with local and/or nonlocal label fusion (so-called "multiatlas segmentation" methods (Coupé et al, 2011, Heckemann, Hajnal, Aljabar, Rueckert, & Hammers, 2006, Iglesias & Sabuncu, 2015). Indeed, many state-of-the-art results (e.g., hippocampus segmentation (Zandifar, Fonov, Coupé, Pruessner, & Collins, 2017) and brain extraction (Novosad & Collins, 2018) exploit a complementary combination of both multiatlas segmentation and machine-learning methods (e.g., error correction (EC) (Wang et al, 2011)).…”
Section: Introductionmentioning
confidence: 99%
“…The left hippocampus is overlaid in green, and the right hippocampus in blue. Errors are overlaid in red in columns four and six Compared to the best method fromZandifar et al (2017), which combines PB segmentation with nonlinear registration and EC (PBS + NLR + EC), our best performing method (CNN-SP-D + DA) yielded an improvement of 2.1% in terms of mean Dice and a decrease in mean MHD of 0.17 mm (over both left and right hippocampi), both of which were highly statistically significant (p ≤ 10 −9 ). CNN-SP-D + DA was also considerably more robust than the methods examined in the work of Zandifar et al, producing fewer outliers with low overlap (Figure 5).…”
Neuroanatomical segmentation in magnetic resonance imaging (MRI) of the brain is a prerequisite for quantitative volume, thickness, and shape measurements, as well as an important intermediate step in many preprocessing pipelines. This work introduces a new highly accurate and versatile method based on 3D convolutional neural networks for the automatic segmentation of neuroanatomy in T1-weighted MRI. In combination with a deep 3D fully convolutional architecture, efficient linear registration-derived spatial priors are used to incorporate additional spatial context into the network. An aggressive data augmentation scheme using random elastic deformations is also used to regularize the networks, allowing for excellent performance even in cases where only limited labeled training data are available. Applied to hippocampus segmentation in an elderly population (mean Dice coefficient = 92.1%) and subcortical segmentation in a healthy adult population (mean Dice coefficient = 89.5%), we demonstrate new state-ofthe-art accuracies and a high robustness to outliers. Further validation on a multistructure segmentation task in a scan-rescan dataset demonstrates accuracy (mean Dice coefficient = 86.6%) similar to the scan-rescan reliability of expert manual segmentations (mean Dice coefficient = 86.9%), and improved reliability compared to both expert manual segmentations and automated segmentations using FIRST. Furthermore, our method maintains a highly competitive runtime performance (e.g., requiring only 10 s for left/ right hippocampal segmentation in 1 × 1 × 1 mm 3 MNI stereotaxic space), orders of magnitude faster than conventional multiatlas segmentation methods.
K E Y W O R D Sdeep learning, magnetic resonance imaging, neural networks, neuroanatomy, segmentation, spatial priors † Data used in preparation of this article were obtained from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database (adni.loni.usc.edu). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. A complete listing of ADNI investigators can be found at
“…Twenty subjects were selected from each of the following clinical subgroups: normal controls, mild cognitive impairment, and Alzheimer's disease. Since this dataset was previously used to compare several state‐of‐the‐art algorithms (Zandifar et al, ), for our experiments, we use the same data (e.g., previously preprocessed as described in Zandifar et al) to enable meaningful comparisons with the results reported in the aforementioned work. Pre‐processing consisted of patch‐based (PB) denoising (Coupé et al, ), N3 nonuniformity correction (Sled, Zijdenbos, & Evans, ), linear intensity normalization to the range [0,100], and affine registration to the MNI‐ICBM152 template (Fonov et al, ) with 1 × 1 × 1 mm 3 resolution.…”
Section: Experiments and Resultsmentioning
confidence: 99%
“…We further compared several variants of our CNN‐based method with several other popular and/or state‐of‐the‐art segmentation methods on the same dataset using the segmentations previously produced in the work of Zandifar et al (), which includes results for four different methods, both before and after applying EC (Wang et al, ), a machine learning based wrapper which attempts to correct systematic errors made by the initial host segmentation method. The methods included are FreeSurfer (Fischl, ), ANIMAL (Collins & Pruessner, ) (a multiatlas technique combining nonlinear registration with majority‐vote label fusion), traditional PB segmentation (Coupé et al, ) (a multiatlas technique combining linear registration with PB label fusion), and an augmented approach combining PB segmentation with nonlinear registration.…”
Section: Experiments and Resultsmentioning
confidence: 99%
“…Note that the results from the 2.5D CNN method (Kushibar et al, 2018) are not included in the boxplots because only summary statistics were available. Of our CNN-based methods, the performance of the baseline network CNN-B was poorest overall T A B L E 5 Comparison of four of our CNN-based segmentation methods with previously reported results (Zandifar et al, 2017)…”
Section: Subcortical Segmentation In the Ibsr Datasetmentioning
confidence: 89%
“…Some such methods have attempted to learn complex mappings between image features and labels using traditional machine-learning based classifiers (e.g., support vector machines (Boser, Guyon, & Vapnik, 1992) and random forests (Breiman, 2001)) combined with handcrafted feature sets (Morra et al, 2010;Zikic et al, 2012), while others have found success transferring labels using a combination of linear or nonlinear image registration with local and/or nonlocal label fusion (so-called "multiatlas segmentation" methods (Coupé et al, 2011, Heckemann, Hajnal, Aljabar, Rueckert, & Hammers, 2006, Iglesias & Sabuncu, 2015). Indeed, many state-of-the-art results (e.g., hippocampus segmentation (Zandifar, Fonov, Coupé, Pruessner, & Collins, 2017) and brain extraction (Novosad & Collins, 2018) exploit a complementary combination of both multiatlas segmentation and machine-learning methods (e.g., error correction (EC) (Wang et al, 2011)).…”
Section: Introductionmentioning
confidence: 99%
“…The left hippocampus is overlaid in green, and the right hippocampus in blue. Errors are overlaid in red in columns four and six Compared to the best method fromZandifar et al (2017), which combines PB segmentation with nonlinear registration and EC (PBS + NLR + EC), our best performing method (CNN-SP-D + DA) yielded an improvement of 2.1% in terms of mean Dice and a decrease in mean MHD of 0.17 mm (over both left and right hippocampi), both of which were highly statistically significant (p ≤ 10 −9 ). CNN-SP-D + DA was also considerably more robust than the methods examined in the work of Zandifar et al, producing fewer outliers with low overlap (Figure 5).…”
Neuroanatomical segmentation in magnetic resonance imaging (MRI) of the brain is a prerequisite for quantitative volume, thickness, and shape measurements, as well as an important intermediate step in many preprocessing pipelines. This work introduces a new highly accurate and versatile method based on 3D convolutional neural networks for the automatic segmentation of neuroanatomy in T1-weighted MRI. In combination with a deep 3D fully convolutional architecture, efficient linear registration-derived spatial priors are used to incorporate additional spatial context into the network. An aggressive data augmentation scheme using random elastic deformations is also used to regularize the networks, allowing for excellent performance even in cases where only limited labeled training data are available. Applied to hippocampus segmentation in an elderly population (mean Dice coefficient = 92.1%) and subcortical segmentation in a healthy adult population (mean Dice coefficient = 89.5%), we demonstrate new state-ofthe-art accuracies and a high robustness to outliers. Further validation on a multistructure segmentation task in a scan-rescan dataset demonstrates accuracy (mean Dice coefficient = 86.6%) similar to the scan-rescan reliability of expert manual segmentations (mean Dice coefficient = 86.9%), and improved reliability compared to both expert manual segmentations and automated segmentations using FIRST. Furthermore, our method maintains a highly competitive runtime performance (e.g., requiring only 10 s for left/ right hippocampal segmentation in 1 × 1 × 1 mm 3 MNI stereotaxic space), orders of magnitude faster than conventional multiatlas segmentation methods.
K E Y W O R D Sdeep learning, magnetic resonance imaging, neural networks, neuroanatomy, segmentation, spatial priors † Data used in preparation of this article were obtained from the Alzheimer's Disease Neuroimaging Initiative (ADNI) database (adni.loni.usc.edu). As such, the investigators within the ADNI contributed to the design and implementation of ADNI and/or provided data but did not participate in analysis or writing of this report. A complete listing of ADNI investigators can be found at
Background: Magnetic resonance imaging (MRI) has become important in the diagnostic work-up of neurodegenerative diseases. icobrain dm, a CE-labeled and FDA-cleared automated brain volumetry software, has shown potential in differentiating cognitively healthy controls (HC) from Alzheimer's disease (AD) dementia (ADD) patients in selected research cohorts.Objective: This study examines the diagnostic value of icobrain dm for AD in routine clinical practice, including a comparison to the widely used FreeSurfer software, and investigates if combined brain volumes contribute to establish an AD diagnosis. Methods: The study population included HC (n = 90), subjective cognitive decline (SCD, n = 93), mild cognitive impairment (MCI, n = 357), and ADD (n = 280) patients. Through automated volumetric analyses of global, cortical, and subcortical brain structures on clinical brain MRI T1w (n = 820) images from a retrospective, multi-center study (REMEMBER), icobrain dm's (v.4.4.0) ability to differentiate disease stages via ROC analysis was compared to FreeSurfer (v.6.0). Stepwise backward regression models were constructed to investigate if combined brain volumes can differentiate between AD stages. Results: icobrain dm outperformed FreeSurfer in processing time (15-30 min versus 9-32 h), robustness (0 versus 67 failures), and diagnostic performance for whole brain, hippocampal volumes, and lateral ventricles between HC and ADD patients. Stepwise backward regression showed improved diagnostic accuracy for pairwise group differentiations, with highest performance obtained for distinguishing HC from ADD (AUC = 0.914; Specificity 83.0%; Sensitivity 86.3%). Conclusion: Automated volumetry has a diagnostic value for ADD diagnosis in routine clinical practice. Our findings indicate that combined brain volumes improve diagnostic accuracy, using real-world imaging data from a clinical setting.
Brain extraction is an important first step in many magnetic resonance neuroimaging studies. Due to variability in brain morphology and in the appearance of the brain due to differences in scanner acquisition parameters, the development of a generally applicable brain extraction algorithm has proven challenging. Learning-based brain extraction algorithms in particular perform well when the target and training images are sufficiently similar, but often perform worse when this condition is not met. In this study, we propose a new patch-based multi-atlas segmentation method for brain extraction which is specifically developed for accurate and robust processing across datasets. Using a diverse collection of labeled images from 5 different datasets, extensive comparisons were made with 9 other commonly used brain extraction methods, both before and after applying error correction (a machine learning method for automatically correcting segmentation errors) to each method. The proposed method performed equal to or better than the other methods in each of two segmentation scenarios: a challenging inter-dataset segmentation scenario in which no dataset-specific atlases were used (mean Dice coefficient 98.57%, volumetric correlation 0.994 across datasets following error correction), and an intra-dataset segmentation scenario in which only dataset-specific atlases were used (mean Dice coefficient 99.02%, volumetric correlation 0.998 across datasets following error correction). Furthermore, combined with error correction, the proposed method runs in less than one-tenth of the time required by the other top-performing methods in the challenging inter-dataset comparisons. Validation on an independent multi-centre dataset also confirmed the excellent performance of the proposed method.
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