Brain-PET image reconstruction methods affect software-aided diagnosis in patients with neurodegenerative diseases

Objectives: The introduction of new developments in neuro-PET, such as digital silicon photomultiplier detectors, time-of-flight (TOF), point-spread-function (PSF) modelling and penalized reconstruction methods has resulted in improved spatial resolution and signal to noise ratio in reconstructed im...

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Veröffentlicht in:The Journal of nuclear medicine (1978) 2018-05, Vol.59, p.1780
Hauptverfasser: Lindstrom, Elin, Danfors, Torsten, Lindsjo, Lars, Lubberink, Mark
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Danfors, Torsten
Lindsjo, Lars
Lubberink, Mark
description Objectives: The introduction of new developments in neuro-PET, such as digital silicon photomultiplier detectors, time-of-flight (TOF), point-spread-function (PSF) modelling and penalized reconstruction methods has resulted in improved spatial resolution and signal to noise ratio in reconstructed images. The objective of this study was to investigate how the improved PET image reconstruction affects quantitative outcome measures and software-aided assessing of patient pathologies. Methods: Twenty-four subjects with 18F-FDG PET examinations, 15 neurodegenerative disease subjects and 9 melanoma subjects without brain involvement (normal controls), scanned on a digital TOF PET/CT scanner, were included in the study. All subjects received 3 MBq/kg, patients were scanned for 10 min starting 45 min post injection, whereas controls were scanned circa 70 min post injection during 2 min. Two reconstruction methods were used; ordered subsets expectation maximization (OSEM; 3 iterations, 16/34 subsets, 3/5 mm Gaussian postfilter, +/- TOF, +/- PSF modelling) and block-sequential regularized expectation maximization (BSREM) (TOF, PSF, penalty regularization parameter β of 75, 150, 225, and 300). A 256 by 256 matrix over a 25 cm FOV was used. Each reconstructed image was anatomically normalized into template space using Cortex ID Suite software (GE Healthcare). Automated analysis of tracer uptake in 26 regions of interest and comparison with the corresponding tracer uptake in normal subjects in terms of z-scores was performed using the whole brain as reference area. Results: TOF, PSF modelling and BSREM gradually increased the relative uptake difference to the normal subjects' database within the software, i.e. resulting in decreasing z-scores. The controls of the study yielded similar results to the normal database when using OSEM 3/16 5 mm reconstruction, without TOF and PSF, with a mean z-score of -0.3. BSREM with β 150, OSEM-TOF-PSF 3/34 3 mm and 5 mm resulted in average z-scores of -1.2, -0.99, and -0.62, respectively. Reducing the filter from 5 to 3 mm decreased z-scores between 19% and 33%, while increasing the number of subsets from 16 to 34 decreased z-scores by 6-29%. Use of TOF with OSEM resulted in slightly decreased z-scores of 1-12%. PSF modelling also decreased z-scores by 9% to 28%. BSREM reconstruction resulted in reduced z-scores compared to OSEM reconstructions regardless of β, the z-score difference to OSEM 3/16 5 mm was -0.96, -0.71, -0.59, and -0.4
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The objective of this study was to investigate how the improved PET image reconstruction affects quantitative outcome measures and software-aided assessing of patient pathologies. Methods: Twenty-four subjects with 18F-FDG PET examinations, 15 neurodegenerative disease subjects and 9 melanoma subjects without brain involvement (normal controls), scanned on a digital TOF PET/CT scanner, were included in the study. All subjects received 3 MBq/kg, patients were scanned for 10 min starting 45 min post injection, whereas controls were scanned circa 70 min post injection during 2 min. Two reconstruction methods were used; ordered subsets expectation maximization (OSEM; 3 iterations, 16/34 subsets, 3/5 mm Gaussian postfilter, +/- TOF, +/- PSF modelling) and block-sequential regularized expectation maximization (BSREM) (TOF, PSF, penalty regularization parameter β of 75, 150, 225, and 300). A 256 by 256 matrix over a 25 cm FOV was used. Each reconstructed image was anatomically normalized into template space using Cortex ID Suite software (GE Healthcare). Automated analysis of tracer uptake in 26 regions of interest and comparison with the corresponding tracer uptake in normal subjects in terms of z-scores was performed using the whole brain as reference area. Results: TOF, PSF modelling and BSREM gradually increased the relative uptake difference to the normal subjects' database within the software, i.e. resulting in decreasing z-scores. The controls of the study yielded similar results to the normal database when using OSEM 3/16 5 mm reconstruction, without TOF and PSF, with a mean z-score of -0.3. BSREM with β 150, OSEM-TOF-PSF 3/34 3 mm and 5 mm resulted in average z-scores of -1.2, -0.99, and -0.62, respectively. Reducing the filter from 5 to 3 mm decreased z-scores between 19% and 33%, while increasing the number of subsets from 16 to 34 decreased z-scores by 6-29%. Use of TOF with OSEM resulted in slightly decreased z-scores of 1-12%. PSF modelling also decreased z-scores by 9% to 28%. BSREM reconstruction resulted in reduced z-scores compared to OSEM reconstructions regardless of β, the z-score difference to OSEM 3/16 5 mm was -0.96, -0.71, -0.59, and -0.46 for β 75, 150, 225 and 300, respectively. Within the patient group, 6.2±2.8 (range, 2-11) regions per patient were assessed as pathologic (z-score &lt; -2) when using the OSEM 3/16 5 mm reconstructed data, compared to 9.0±2.8 (range, 4-14) regions per patient using BSREM with β 150. In the controls, 2.2±2.0 (range, 0-6) and 6.2±2.0 (range, 3-9) regions per subject would be considered pathologic using OSEM 3/16 5 mm and BSREM β 150, respectively. Conclusions: Based on the findings of this study, software-aided diagnosis is affected by image reconstruction methods and parameter settings. The number of regions identified as pathological tends to increase in both patients and normal controls using image quality enhancement tools, such as TOF, PSF modelling and BSREM reconstruction. To avoid false-positive results, software-aided diagnosis should be used with caution when employing improved image reconstruction methods compared to those used for acquisition of the normal database.</description><identifier>ISSN: 0161-5505</identifier><identifier>EISSN: 1535-5667</identifier><language>eng</language><publisher>New York: Society of Nuclear Medicine</publisher><subject>Brain ; Computed tomography ; Computer programs ; Diagnosis ; Identification methods ; Image acquisition ; Image enhancement ; Image processing ; Image quality ; Image reconstruction ; Injection ; Mathematical models ; Maximization ; Medical diagnosis ; Medical imaging ; Melanoma ; Modelling ; Neurodegenerative diseases ; Neuroimaging ; Optimization ; Parameter identification ; Patients ; Photomultiplier tubes ; Positron emission ; Positron emission tomography ; Regularization ; Signal to noise ratio ; Software ; Spatial discrimination ; Spatial resolution ; Tomography</subject><ispartof>The Journal of nuclear medicine (1978), 2018-05, Vol.59, p.1780</ispartof><rights>Copyright Society of Nuclear Medicine May 1, 2018</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781</link.rule.ids></links><search><creatorcontrib>Lindstrom, Elin</creatorcontrib><creatorcontrib>Danfors, Torsten</creatorcontrib><creatorcontrib>Lindsjo, Lars</creatorcontrib><creatorcontrib>Lubberink, Mark</creatorcontrib><title>Brain-PET image reconstruction methods affect software-aided diagnosis in patients with neurodegenerative diseases</title><title>The Journal of nuclear medicine (1978)</title><description>Objectives: The introduction of new developments in neuro-PET, such as digital silicon photomultiplier detectors, time-of-flight (TOF), point-spread-function (PSF) modelling and penalized reconstruction methods has resulted in improved spatial resolution and signal to noise ratio in reconstructed images. The objective of this study was to investigate how the improved PET image reconstruction affects quantitative outcome measures and software-aided assessing of patient pathologies. Methods: Twenty-four subjects with 18F-FDG PET examinations, 15 neurodegenerative disease subjects and 9 melanoma subjects without brain involvement (normal controls), scanned on a digital TOF PET/CT scanner, were included in the study. All subjects received 3 MBq/kg, patients were scanned for 10 min starting 45 min post injection, whereas controls were scanned circa 70 min post injection during 2 min. Two reconstruction methods were used; ordered subsets expectation maximization (OSEM; 3 iterations, 16/34 subsets, 3/5 mm Gaussian postfilter, +/- TOF, +/- PSF modelling) and block-sequential regularized expectation maximization (BSREM) (TOF, PSF, penalty regularization parameter β of 75, 150, 225, and 300). A 256 by 256 matrix over a 25 cm FOV was used. Each reconstructed image was anatomically normalized into template space using Cortex ID Suite software (GE Healthcare). Automated analysis of tracer uptake in 26 regions of interest and comparison with the corresponding tracer uptake in normal subjects in terms of z-scores was performed using the whole brain as reference area. Results: TOF, PSF modelling and BSREM gradually increased the relative uptake difference to the normal subjects' database within the software, i.e. resulting in decreasing z-scores. The controls of the study yielded similar results to the normal database when using OSEM 3/16 5 mm reconstruction, without TOF and PSF, with a mean z-score of -0.3. BSREM with β 150, OSEM-TOF-PSF 3/34 3 mm and 5 mm resulted in average z-scores of -1.2, -0.99, and -0.62, respectively. Reducing the filter from 5 to 3 mm decreased z-scores between 19% and 33%, while increasing the number of subsets from 16 to 34 decreased z-scores by 6-29%. Use of TOF with OSEM resulted in slightly decreased z-scores of 1-12%. PSF modelling also decreased z-scores by 9% to 28%. BSREM reconstruction resulted in reduced z-scores compared to OSEM reconstructions regardless of β, the z-score difference to OSEM 3/16 5 mm was -0.96, -0.71, -0.59, and -0.46 for β 75, 150, 225 and 300, respectively. Within the patient group, 6.2±2.8 (range, 2-11) regions per patient were assessed as pathologic (z-score &lt; -2) when using the OSEM 3/16 5 mm reconstructed data, compared to 9.0±2.8 (range, 4-14) regions per patient using BSREM with β 150. In the controls, 2.2±2.0 (range, 0-6) and 6.2±2.0 (range, 3-9) regions per subject would be considered pathologic using OSEM 3/16 5 mm and BSREM β 150, respectively. Conclusions: Based on the findings of this study, software-aided diagnosis is affected by image reconstruction methods and parameter settings. The number of regions identified as pathological tends to increase in both patients and normal controls using image quality enhancement tools, such as TOF, PSF modelling and BSREM reconstruction. 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Danfors, Torsten ; Lindsjo, Lars ; Lubberink, Mark</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_24355481803</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Brain</topic><topic>Computed tomography</topic><topic>Computer programs</topic><topic>Diagnosis</topic><topic>Identification methods</topic><topic>Image acquisition</topic><topic>Image enhancement</topic><topic>Image processing</topic><topic>Image quality</topic><topic>Image reconstruction</topic><topic>Injection</topic><topic>Mathematical models</topic><topic>Maximization</topic><topic>Medical diagnosis</topic><topic>Medical imaging</topic><topic>Melanoma</topic><topic>Modelling</topic><topic>Neurodegenerative diseases</topic><topic>Neuroimaging</topic><topic>Optimization</topic><topic>Parameter identification</topic><topic>Patients</topic><topic>Photomultiplier tubes</topic><topic>Positron emission</topic><topic>Positron emission tomography</topic><topic>Regularization</topic><topic>Signal to noise ratio</topic><topic>Software</topic><topic>Spatial discrimination</topic><topic>Spatial resolution</topic><topic>Tomography</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lindstrom, Elin</creatorcontrib><creatorcontrib>Danfors, Torsten</creatorcontrib><creatorcontrib>Lindsjo, Lars</creatorcontrib><creatorcontrib>Lubberink, Mark</creatorcontrib><collection>Docstoc</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biochemistry Abstracts 1</collection><collection>Nursing &amp; Allied Health Premium</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>The Journal of nuclear medicine (1978)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lindstrom, Elin</au><au>Danfors, Torsten</au><au>Lindsjo, Lars</au><au>Lubberink, Mark</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Brain-PET image reconstruction methods affect software-aided diagnosis in patients with neurodegenerative diseases</atitle><jtitle>The Journal of nuclear medicine (1978)</jtitle><date>2018-05-01</date><risdate>2018</risdate><volume>59</volume><spage>1780</spage><pages>1780-</pages><issn>0161-5505</issn><eissn>1535-5667</eissn><abstract>Objectives: The introduction of new developments in neuro-PET, such as digital silicon photomultiplier detectors, time-of-flight (TOF), point-spread-function (PSF) modelling and penalized reconstruction methods has resulted in improved spatial resolution and signal to noise ratio in reconstructed images. The objective of this study was to investigate how the improved PET image reconstruction affects quantitative outcome measures and software-aided assessing of patient pathologies. Methods: Twenty-four subjects with 18F-FDG PET examinations, 15 neurodegenerative disease subjects and 9 melanoma subjects without brain involvement (normal controls), scanned on a digital TOF PET/CT scanner, were included in the study. All subjects received 3 MBq/kg, patients were scanned for 10 min starting 45 min post injection, whereas controls were scanned circa 70 min post injection during 2 min. Two reconstruction methods were used; ordered subsets expectation maximization (OSEM; 3 iterations, 16/34 subsets, 3/5 mm Gaussian postfilter, +/- TOF, +/- PSF modelling) and block-sequential regularized expectation maximization (BSREM) (TOF, PSF, penalty regularization parameter β of 75, 150, 225, and 300). A 256 by 256 matrix over a 25 cm FOV was used. Each reconstructed image was anatomically normalized into template space using Cortex ID Suite software (GE Healthcare). Automated analysis of tracer uptake in 26 regions of interest and comparison with the corresponding tracer uptake in normal subjects in terms of z-scores was performed using the whole brain as reference area. Results: TOF, PSF modelling and BSREM gradually increased the relative uptake difference to the normal subjects' database within the software, i.e. resulting in decreasing z-scores. The controls of the study yielded similar results to the normal database when using OSEM 3/16 5 mm reconstruction, without TOF and PSF, with a mean z-score of -0.3. BSREM with β 150, OSEM-TOF-PSF 3/34 3 mm and 5 mm resulted in average z-scores of -1.2, -0.99, and -0.62, respectively. Reducing the filter from 5 to 3 mm decreased z-scores between 19% and 33%, while increasing the number of subsets from 16 to 34 decreased z-scores by 6-29%. Use of TOF with OSEM resulted in slightly decreased z-scores of 1-12%. PSF modelling also decreased z-scores by 9% to 28%. BSREM reconstruction resulted in reduced z-scores compared to OSEM reconstructions regardless of β, the z-score difference to OSEM 3/16 5 mm was -0.96, -0.71, -0.59, and -0.46 for β 75, 150, 225 and 300, respectively. Within the patient group, 6.2±2.8 (range, 2-11) regions per patient were assessed as pathologic (z-score &lt; -2) when using the OSEM 3/16 5 mm reconstructed data, compared to 9.0±2.8 (range, 4-14) regions per patient using BSREM with β 150. In the controls, 2.2±2.0 (range, 0-6) and 6.2±2.0 (range, 3-9) regions per subject would be considered pathologic using OSEM 3/16 5 mm and BSREM β 150, respectively. Conclusions: Based on the findings of this study, software-aided diagnosis is affected by image reconstruction methods and parameter settings. The number of regions identified as pathological tends to increase in both patients and normal controls using image quality enhancement tools, such as TOF, PSF modelling and BSREM reconstruction. To avoid false-positive results, software-aided diagnosis should be used with caution when employing improved image reconstruction methods compared to those used for acquisition of the normal database.</abstract><cop>New York</cop><pub>Society of Nuclear Medicine</pub></addata></record>
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subjects Brain
Computed tomography
Computer programs
Diagnosis
Identification methods
Image acquisition
Image enhancement
Image processing
Image quality
Image reconstruction
Injection
Mathematical models
Maximization
Medical diagnosis
Medical imaging
Melanoma
Modelling
Neurodegenerative diseases
Neuroimaging
Optimization
Parameter identification
Patients
Photomultiplier tubes
Positron emission
Positron emission tomography
Regularization
Signal to noise ratio
Software
Spatial discrimination
Spatial resolution
Tomography
title Brain-PET image reconstruction methods affect software-aided diagnosis in patients with neurodegenerative diseases
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