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      Accurate hybrid template–based and MR-based attenuation correction using UTE images for simultaneous PET/MR brain imaging applications

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          Abstract

          Background

          Attenuation correction is one of the most crucial correction factors for accurate PET data quantitation in hybrid PET/MR scanners, and computing accurate attenuation coefficient maps from MR brain acquisitions is challenging. Here, we develop a method for accurate bone and air segmentation using MR ultrashort echo time (UTE) images.

          Methods

          MR UTE images from simultaneous MR and PET imaging of five healthy volunteers was used to generate a whole head, bone and air template image for inclusion into an improved MR derived attenuation correction map, and applied to PET image data for quantitative analysis. Bone, air and soft tissue were segmented based on Gaussian Mixture Models with probabilistic tissue maps as a priori information. We present results for two approaches for bone attenuation coefficient assignments: one using a constant attenuation correction value; and another using an estimated continuous attenuation value based on a calibration fit. Quantitative comparisons were performed to evaluate the accuracy of the reconstructed PET images, with respect to a reference image reconstructed with manually segmented attenuation maps.

          Results

          The DICE coefficient analysis for the air and bone regions in the images demonstrated improvements compared to the UTE approach, and other state-of-the-art techniques. The most accurate whole brain and regional brain analyses were obtained using constant bone attenuation coefficient values.

          Conclusions

          A novel attenuation correction method for PET data reconstruction is proposed. Analyses show improvements in the quantitative accuracy of the reconstructed PET images compared to other state-of-the-art AC methods for simultaneous PET/MR scanners. Further evaluation is needed with radiopharmaceuticals other than FDG, and in larger cohorts of participants.

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          Most cited references44

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          Deep Learning MR Imaging–based Attenuation Correction for PET/MR Imaging

          Purpose To develop and evaluate the feasibility of deep learning approaches for magnetic resonance (MR) imaging-based attenuation correction (AC) (termed deep MRAC) in brain positron emission tomography (PET)/MR imaging. Materials and Methods A PET/MR imaging AC pipeline was built by using a deep learning approach to generate pseudo computed tomographic (CT) scans from MR images. A deep convolutional auto-encoder network was trained to identify air, bone, and soft tissue in volumetric head MR images coregistered to CT data for training. A set of 30 retrospective three-dimensional T1-weighted head images was used to train the model, which was then evaluated in 10 patients by comparing the generated pseudo CT scan to an acquired CT scan. A prospective study was carried out for utilizing simultaneous PET/MR imaging for five subjects by using the proposed approach. Analysis of covariance and paired-sample t tests were used for statistical analysis to compare PET reconstruction error with deep MRAC and two existing MR imaging-based AC approaches with CT-based AC. Results Deep MRAC provides an accurate pseudo CT scan with a mean Dice coefficient of 0.971 ± 0.005 for air, 0.936 ± 0.011 for soft tissue, and 0.803 ± 0.021 for bone. Furthermore, deep MRAC provides good PET results, with average errors of less than 1% in most brain regions. Significantly lower PET reconstruction errors were realized with deep MRAC (-0.7% ± 1.1) compared with Dixon-based soft-tissue and air segmentation (-5.8% ± 3.1) and anatomic CT-based template registration (-4.8% ± 2.2). Conclusion The authors developed an automated approach that allows generation of discrete-valued pseudo CT scans (soft tissue, bone, and air) from a single high-spatial-resolution diagnostic-quality three-dimensional MR image and evaluated it in brain PET/MR imaging. This deep learning approach for MR imaging-based AC provided reduced PET reconstruction error relative to a CT-based standard within the brain compared with current MR imaging-based AC approaches. © RSNA, 2017 Online supplemental material is available for this article.
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            MRI-based attenuation correction for PET/MRI using ultrashort echo time sequences.

            One of the challenges in PET/MRI is the derivation of an attenuation map to correct the PET image for attenuation. Different methods have been suggested for deriving the attenuation map from an MR image. Because the low signal intensity of cortical bone on images acquired with conventional MRI sequences makes it difficult to detect this tissue type, these methods rely on some sort of anatomic precondition to predict the attenuation map, raising the question of whether these methods will be usable in the clinic when patients may exhibit anatomic abnormalities. We propose the use of the transverse relaxation rate, derived from images acquired with an ultrashort echo time sequence to classify the voxels into 1 of 3 tissue classes (bone, soft tissue, or air), without making any assumptions on patient anatomy. Each voxel is assigned a linear attenuation coefficient corresponding to its tissue class. A reference CT scan is used to determine the voxel-by-voxel accuracy of the proposed method. The overall accuracy of the MRI-based attenuation correction is evaluated using a method that takes into account the nonlocal effects of attenuation correction. As a proof of concept, the head of a pig was used as a phantom for imaging. The new method yielded a correct tissue classification in 90% of the voxels. Five human brain PET/CT and MRI datasets were also processed, yielding slightly worse voxel-by-voxel performance, compared to a CT-derived attenuation map. The PET datasets were reconstructed using the segmented MRI attenuation map derived with the new method, and the resulting images were compared with segmented CT-based attenuation correction. An average error of around 5% was found in the brain. The feasibility of using the transverse relaxation rate map derived from ultrashort echo time MR images for the estimation of the attenuation map was shown on phantom and clinical brain data. The results indicate that the new method, compared with CT-based attenuation correction, yields clinically acceptable errors. The proposed method does not make any assumptions about patient anatomy and could therefore also be used in cases in which anatomic abnormalities are present.
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              Attenuation correction for a combined 3D PET/CT scanner.

              In this work we demonstrate the proof of principle of CT-based attenuation correction of 3D positron emission tomography (PET) data by using scans of bone and soft tissue equivalent phantoms and scans of humans. This method of attenuation correction is intended for use in a single scanner that combines volume-imaging (3D) PET with x-ray computed tomography (CT) for the purpose of providing accurately registered anatomical localization of structures seen in the PET image. The goal of this work is to determine if we can perform attenuation correction of the PET emission data using accurately aligned CT attenuation information. We discuss possible methods of calculating the PET attenuation map at 511 keV based on CT transmission information acquired from 40 keV through 140 keV. Data were acquired on separate CT and PET scanners and were aligned using standard image registration procedures. Results are presented on three of the attenuation calculation methods: segmentation, scaling, and our proposed hybrid segmentation/scaling method. The results are compared with those using the standard 3D PET attenuation correction method as a gold standard. We demonstrate the efficacy of our proposed hybrid method for converting the CT attenuation map from an effective CT photon energy of 70 keV to the PET photon energy of 511 keV. We conclude that using CT information is a feasible way to obtain attenuation correction factors for 3D PET.
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                Author and article information

                Contributors
                +48 534 065 750 , jakubbaran92@gmail.com
                zhaolin.chen@monash.edu
                francesco.sforazzini@gmail.com
                nicholas.ferris@monash.edu
                sharna.jamadar@monash.edu
                benjamin_schmitt@siemens-healthineers.com
                david.faul@siemens-healthineers.com
                n.j.shah@fz-juelich.de
                mcholewa@ur.edu.pl
                gary.egan@monash.edu
                Journal
                BMC Med Imaging
                BMC Med Imaging
                BMC Medical Imaging
                BioMed Central (London )
                1471-2342
                6 November 2018
                6 November 2018
                2018
                : 18
                : 41
                Affiliations
                [1 ]ISNI 0000 0004 1936 7857, GRID grid.1002.3, Monash Biomedical Imaging, , Monash University, ; Melbourne, Australia
                [2 ]ISNI 0000 0001 2154 3176, GRID grid.13856.39, Department of Biophysics, Faculty of Mathematics and Natural Sciences, , University of Rzeszow, ; Rzeszow, Poland
                [3 ]ISNI 0000 0001 1958 0162, GRID grid.413454.3, Institute of Nuclear Science Polish Academy of Science, ; Krakow, Poland
                [4 ]ISNI 0000 0004 1936 7857, GRID grid.1002.3, Department of Electrical and Computer Systems Engineering, , Monash University, ; Melbourne, Australia
                [5 ]ISNI 0000 0000 9295 3933, GRID grid.419789.a, Monash Imaging, Monash Health, ; Clayton, Australia
                [6 ]ISNI 0000 0004 1936 7857, GRID grid.1002.3, Monash Institute of Cognitive and Clinical Neurosciences and School of Psychological Sciences, , Monash University, ; Melbourne, Australia
                [7 ]ISNI 0000 0004 1936 7857, GRID grid.1002.3, Australian Research Council Centre of Excellence for Integrative Brain Function, , Monash University, ; Melbourne, Australia
                [8 ]Siemens Healthcare Pty Ltd, Sydney, Australia
                [9 ]Siemens Healthcare Pty Ltd, New York, USA
                [10 ]ISNI 0000 0001 2297 375X, GRID grid.8385.6, Institute of Neuroscience and Medicine, Forschungszentrum Juelich GmbH, ; Juelich, Germany
                Author information
                http://orcid.org/0000-0002-4946-3837
                Article
                283
                10.1186/s12880-018-0283-3
                6220492
                30400875
                b188ed65-f74b-4b46-b48e-190536aac316
                © The Author(s). 2018

                Open AccessThis 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
                : 1 August 2018
                : 24 October 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100000923, Australian Research Council;
                Award ID: CE1400007
                Award Recipient :
                Funded by: ARC Discovery Early Career Researcher
                Award ID: DE150100406
                Award Recipient :
                Funded by: Reignwood Cultural Foundation
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2018

                Radiology & Imaging
                pet/mr,attenuation correction,brain,ute
                Radiology & Imaging
                pet/mr, attenuation correction, brain, ute

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