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      Automated cardiovascular magnetic resonance image analysis with fully convolutional networks

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          Abstract

          Background

          Cardiovascular resonance (CMR) imaging is a standard imaging modality for assessing cardiovascular diseases (CVDs), the leading cause of death globally. CMR enables accurate quantification of the cardiac chamber volume, ejection fraction and myocardial mass, providing information for diagnosis and monitoring of CVDs. However, for years, clinicians have been relying on manual approaches for CMR image analysis, which is time consuming and prone to subjective errors. It is a major clinical challenge to automatically derive quantitative and clinically relevant information from CMR images.

          Methods

          Deep neural networks have shown a great potential in image pattern recognition and segmentation for a variety of tasks. Here we demonstrate an automated analysis method for CMR images, which is based on a fully convolutional network (FCN). The network is trained and evaluated on a large-scale dataset from the UK Biobank, consisting of 4,875 subjects with 93,500 pixelwise annotated images. The performance of the method has been evaluated using a number of technical metrics, including the Dice metric, mean contour distance and Hausdorff distance, as well as clinically relevant measures, including left ventricle (LV) end-diastolic volume (LVEDV) and end-systolic volume (LVESV), LV mass (LVM); right ventricle (RV) end-diastolic volume (RVEDV) and end-systolic volume (RVESV).

          Results

          By combining FCN with a large-scale annotated dataset, the proposed automated method achieves a high performance in segmenting the LV and RV on short-axis CMR images and the left atrium (LA) and right atrium (RA) on long-axis CMR images. On a short-axis image test set of 600 subjects, it achieves an average Dice metric of 0.94 for the LV cavity, 0.88 for the LV myocardium and 0.90 for the RV cavity. The mean absolute difference between automated measurement and manual measurement is 6.1 mL for LVEDV, 5.3 mL for LVESV, 6.9 gram for LVM, 8.5 mL for RVEDV and 7.2 mL for RVESV. On long-axis image test sets, the average Dice metric is 0.93 for the LA cavity (2-chamber view), 0.95 for the LA cavity (4-chamber view) and 0.96 for the RA cavity (4-chamber view). The performance is comparable to human inter-observer variability.

          Conclusions

          We show that an automated method achieves a performance on par with human experts in analysing CMR images and deriving clinically relevant measures.

          Electronic supplementary material

          The online version of this article (10.1186/s12968-018-0471-x) contains supplementary material, which is available to authorized users.

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          Most cited references26

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          Dermatologist-level classification of skin cancer with deep neural networks

          Skin cancer, the most common human malignancy, is primarily diagnosed visually, beginning with an initial clinical screening and followed potentially by dermoscopic analysis, a biopsy and histopathological examination. Automated classification of skin lesions using images is a challenging task owing to the fine-grained variability in the appearance of skin lesions. Deep convolutional neural networks (CNNs) show potential for general and highly variable tasks across many fine-grained object categories. Here we demonstrate classification of skin lesions using a single CNN, trained end-to-end from images directly, using only pixels and disease labels as inputs. We train a CNN using a dataset of 129,450 clinical images—two orders of magnitude larger than previous datasets—consisting of 2,032 different diseases. We test its performance against 21 board-certified dermatologists on biopsy-proven clinical images with two critical binary classification use cases: keratinocyte carcinomas versus benign seborrheic keratoses; and malignant melanomas versus benign nevi. The first case represents the identification of the most common cancers, the second represents the identification of the deadliest skin cancer. The CNN achieves performance on par with all tested experts across both tasks, demonstrating an artificial intelligence capable of classifying skin cancer with a level of competence comparable to dermatologists. Outfitted with deep neural networks, mobile devices can potentially extend the reach of dermatologists outside of the clinic. It is projected that 6.3 billion smartphone subscriptions will exist by the year 2021 (ref. 13) and can therefore potentially provide low-cost universal access to vital diagnostic care.
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            Comparison of Sociodemographic and Health-Related Characteristics of UK Biobank Participants With Those of the General Population

            Abstract The UK Biobank cohort is a population-based cohort of 500,000 participants recruited in the United Kingdom (UK) between 2006 and 2010. Approximately 9.2 million individuals aged 40–69 years who lived within 25 miles (40 km) of one of 22 assessment centers in England, Wales, and Scotland were invited to enter the cohort, and 5.5% participated in the baseline assessment. The representativeness of the UK Biobank cohort was investigated by comparing demographic characteristics between nonresponders and responders. Sociodemographic, physical, lifestyle, and health-related characteristics of the cohort were compared with nationally representative data sources. UK Biobank participants were more likely to be older, to be female, and to live in less socioeconomically deprived areas than nonparticipants. Compared with the general population, participants were less likely to be obese, to smoke, and to drink alcohol on a daily basis and had fewer self-reported health conditions. At age 70–74 years, rates of all-cause mortality and total cancer incidence were 46.2% and 11.8% lower, respectively, in men and 55.5% and 18.1% lower, respectively, in women than in the general population of the same age. UK Biobank is not representative of the sampling population; there is evidence of a “healthy volunteer” selection bias. Nonetheless, valid assessment of exposure-disease relationships may be widely generalizable and does not require participants to be representative of the population at large.
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              Mastering the game of Go with deep neural networks and tree search.

              The game of Go has long been viewed as the most challenging of classic games for artificial intelligence owing to its enormous search space and the difficulty of evaluating board positions and moves. Here we introduce a new approach to computer Go that uses 'value networks' to evaluate board positions and 'policy networks' to select moves. These deep neural networks are trained by a novel combination of supervised learning from human expert games, and reinforcement learning from games of self-play. Without any lookahead search, the neural networks play Go at the level of state-of-the-art Monte Carlo tree search programs that simulate thousands of random games of self-play. We also introduce a new search algorithm that combines Monte Carlo simulation with value and policy networks. Using this search algorithm, our program AlphaGo achieved a 99.8% winning rate against other Go programs, and defeated the human European Go champion by 5 games to 0. This is the first time that a computer program has defeated a human professional player in the full-sized game of Go, a feat previously thought to be at least a decade away.
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                Author and article information

                Contributors
                w.bai@imperial.ac.uk
                m.sinclair@imperial.ac.uk
                g.tarroni@imperial.ac.uk
                o.oktay13@imperial.ac.uk
                m.rajchl@imperial.ac.uk
                g.vaillant@imperial.ac.uk
                a.lee@qmul.ac.uk
                n.aung@qmul.ac.uk
                elena.lukaschuk@cardiov.ox.ac.uk
                m.sanghvi@qmul.ac.uk
                filip@zemrak.co.uk
                k.fung@qmul.ac.uk
                j.paiva@qmul.ac.uk
                valentina@simula.no
                dryj@yuhs.ac
                h.suzuki@imperial.ac.uk
                b.kainz@imperial.ac.uk
                p.matthews@imperial.ac.uk
                s.e.petersen@qmul.ac.uk
                stefan.piechnik@cardiov.ox.ac.uk
                stefan.neubauer@cardiov.ox.ac.uk
                b.glocker@imperial.ac.uk
                d.rueckert@imperial.ac.uk
                Journal
                J Cardiovasc Magn Reson
                J Cardiovasc Magn Reson
                Journal of Cardiovascular Magnetic Resonance
                BioMed Central (London )
                1097-6647
                1532-429X
                14 September 2018
                14 September 2018
                2018
                : 20
                : 65
                Affiliations
                [1 ]ISNI 0000 0001 2113 8111, GRID grid.7445.2, Biomedical Image Analysis Group, Department of Computing, Imperial College London, ; London, UK
                [2 ]ISNI 0000 0001 2171 1133, GRID grid.4868.2, NIHR Biomedical Research Centre at Barts, Queen Mary University of London, ; London, UK
                [3 ]ISNI 0000 0004 1936 8948, GRID grid.4991.5, Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, ; Oxford, UK
                [4 ]ISNI 0000 0001 2113 8111, GRID grid.7445.2, Division of Brain Sciences, Department of Medicine, Imperial College London, ; London, UK
                Author information
                http://orcid.org/0000-0003-2943-7698
                Article
                471
                10.1186/s12968-018-0471-x
                6138894
                30217194
                9949e37c-8084-4ff8-872f-027a06e8df94
                © The Author(s) 2018

                Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 23 November 2017
                : 20 June 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100000266, Engineering and Physical Sciences Research Council;
                Award ID: EP/P001009/1
                Categories
                Research
                Custom metadata
                © The Author(s) 2018

                Cardiovascular Medicine
                cmr image analysis,fully convolutional networks,machine learning
                Cardiovascular Medicine
                cmr image analysis, fully convolutional networks, machine learning

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