54 research outputs found
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Deep Learning-based Prescription of Cardiac MRI Planes.
PurposeTo develop and evaluate a system to prescribe imaging planes for cardiac MRI based on deep learning (DL)-based localization of key anatomic landmarks.Materials and methodsAnnotated landmarks on 892 long-axis (LAX) and 493 short-axis (SAX) cine steady-state free precession series from cardiac MR images were retrospectively collected between February 2012 and June 2017. U-Net-based heatmap regression was used for localization of cardiac landmarks, which were used to compute cardiac MRI planes. Performance was evaluated by comparing localization distances and plane angle differences between DL predictions and ground truth. The plane angulations from DL were compared with those prescribed by the technologist at the original time of acquisition. Data were split into 80% for training and 20% for testing, and results confirmed with fivefold cross-validation.ResultsOn LAX images, DL localized the apex within mean 12.56 mm ± 19.11 (standard deviation) and the mitral valve (MV) within 7.68 mm ± 6.91. On SAX images, DL localized the aortic valve within 5.78 mm ± 5.68, MV within 5.90 mm ± 5.24, pulmonary valve within 6.55 mm ± 6.39, and tricuspid valve within 6.39 mm ± 5.89. On the basis of these localizations, average angle bias and mean error of DL-predicted imaging planes relative to ground truth annotations were as follows: SAX, -1.27° ± 6.81 and 4.93° ± 4.86; four chambers, 0.38° ± 6.45 and 5.16° ± 3.80; three chambers, 0.13° ± 12.70 and 9.02° ± 8.83; and two chamber, 0.25° ± 9.08 and 6.53° ± 6.28, respectively.ConclusionDL-based anatomic localization is a feasible strategy for planning cardiac MRI planes. This approach can produce imaging planes comparable to those defined by ground truth landmarks.© RSNA, 2019 Supplemental material is available for this article
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Automated CT and MRI Liver Segmentation and Biometry Using a Generalized Convolutional Neural Network.
PurposeTo assess feasibility of training a convolutional neural network (CNN) to automate liver segmentation across different imaging modalities and techniques used in clinical practice and apply this to enable automation of liver biometry.MethodsWe trained a 2D U-Net CNN for liver segmentation in two stages using 330 abdominal MRI and CT exams acquired at our institution. First, we trained the neural network with non-contrast multi-echo spoiled-gradient-echo (SGPR)images with 300 MRI exams to provide multiple signal-weightings. Then, we used transfer learning to generalize the CNN with additional images from 30 contrast-enhanced MRI and CT exams.We assessed the performance of the CNN using a distinct multi-institutional data set curated from multiple sources (n = 498 subjects). Segmentation accuracy was evaluated by computing Dice scores. Utilizing these segmentations, we computed liver volume from CT and T1-weighted (T1w) MRI exams, and estimated hepatic proton- density-fat-fraction (PDFF) from multi-echo T2*w MRI exams. We compared quantitative volumetry and PDFF estimates between automated and manual segmentation using Pearson correlation and Bland-Altman statistics.ResultsDice scores were 0.94 ± 0.06 for CT (n = 230), 0.95 ± 0.03 (n = 100) for T1w MR, and 0.92 ± 0.05 for T2*w MR (n = 169). Liver volume measured by manual and automated segmentation agreed closely for CT (95% limit-of-agreement (LoA) = [-298 mL, 180 mL]) and T1w MR (LoA = [-358 mL, 180 mL]). Hepatic PDFF measured by the two segmentations also agreed closely (LoA = [-0.62%, 0.80%]).ConclusionsUtilizing a transfer-learning strategy, we have demonstrated the feasibility of a CNN to be generalized to perform liver segmentations across different imaging techniques and modalities. With further refinement and validation, CNNs may have broad applicability for multimodal liver volumetry and hepatic tissue characterization
The interactions of alcohol, sex, and stress
Human history is deeply intertwined with alcohol consumption. While alcohol use disorders (AUD) are often considered on an individual level they represent a societal problem, with increasing evidence for a dichotomy between men and women in their sequelae. It is known that stress impacts all aspects of the addiction cycle and while much work has been focused on the acute use of ethanol or withdrawal, many questions still remain about the transition to dependence and variation between sexes. This study sought to evolve our understanding of the changes occurring within the context of chronic ethanol exposure, as this is an area of investigation poised to significantly impact treatment paradigms. In chapter 2, preclinical studies were performed to elucidate the activation changes occurring in the stress responsive central nucleus of the amygdala (CeA) within chronic ethanol exposure on both a long term and short term scale, and to examine the effect of this chronic ethanol use on the stress response. Next, in chapter 3, anatomical approaches were utilized to link two major monoaminergic nuclei, the locus coeruleus (LC) and the dorsal raphe nucleus (DRN), by virtue of coordinate projections from the limbic stress nucleus, the CeA. The phenotype of these collateralized neurons was then identified as containing the key stress peptides corticotropin releasing factor (CRF) or dynorphin (DYN). Finally, in chapter 4, a molecular marker of the stress response, the CRFr, was examined in the LC using immunoelectron microscopy, and found to be dysregulated in a dichotomous fashion, potentially underlying some of the stress vulnerability seen in AUD. This study offers both molecular and circuitry targets that may be considered in future treatment paradigms, and highlights the importance of individualized treatment strategies for maximal patient benefit.
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Clinical Performance and Role of Expert Supervision of Deep Learning for Cardiac Ventricular Volumetry: A Validation Study
PurposeTo evaluate the performance of a deep learning (DL) algorithm for clinical measurement of right and left ventricular volume and function across cardiac MR images obtained for a range of clinical indications and pathologies.Materials and methodsA retrospective, Health Insurance Portability and Accountability Act-compliant study was conducted using the first 200 noncongenital clinical cardiac MRI examinations from June 2015 to June 2017 for which volumetry was available. Images were analyzed using commercially available software for automated DL-based and manual contouring of biventricular volumes. Fully automated measurements were compared using Pearson correlations, relative volume errors, and Bland-Altman analyses. Manual, automated, and expert revised contours for 50 MR images were examined by comparing regional Dice coefficients at the base, midventricle, and apex to further analyze the contour quality.ResultsFully automated and manual left ventricular volumes were strongly correlated for end-systolic volume (ESV: Pearson r = 0.99, P < .001), end-diastolic volume (EDV: r = 0.97, P < .001), and ejection fraction (EF: r = 0.94, P < .001). Right ventricular measurements were also correlated for ESV (r = 0.93, P < .001), EDV (r = 0.92, P < .001), and EF (r = 0.73, P < .001). Visual inspection of segmentation quality showed most errors (73%) occurred at the cardiac base. Mean Dice coefficients between manual, automated, and expert revised contours ranged from 0.92 to 0.95, with greatest variance at the base and apex.ConclusionFully automated ventricular segmentation by the tested algorithm provides contours and ventricular volumes that could be used to aid expert segmentation, but can benefit from expert supervision, particularly to resolve errors at the basal and apical slices. Supplemental material is available for this article. © RSNA, 2020
Response to letter regarding “Limited Scope for Latitudinal Extension of Reef Corals”
In their recent letter, Madin et al. (2016) dispute our findings in Muir et al. (2015a) that reduced levels of light during winter confine staghorn corals to shallower depths at higher latitudes and will ultimately limit their scope for latitudinal expansion as oceans warm. We based our conclusions on a rich global dataset analysed using two types of analyses: polynomial quantile regression models and species distribution models. Madin and colleagues’ reanalysis of our data focuses only on the quantile regression model, and in our view, provides no convincing quantitative evidence in support of their proposition that most species exhibit either no trend or a reverse trend to the one we described.
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