Use of a Ray-Based Reconstruction Algorithm to Accurately Quantify Preclinical MicroSPECT Images

This work aimed to measure the in vivo quantification errors obtained when ray-based iterative reconstruction is used in micro-single-photon emission computed tomography (SPECT). This was investigated with an extensive phantom-based evaluation and two typical in vivo studies using 99m Tc and 111 In,...

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Main Authors: Bert Vandeghinste, Roel Van Holen, Christian Vanhove, Filip De Vos, Stefaan Vandenberghe, Steven Staelens
Format: Article
Language:English
Published: SAGE Publishing 2014-06-01
Series:Molecular Imaging
Online Access:https://doi.org/10.2310/7290.2014.00007
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author Bert Vandeghinste
Roel Van Holen
Christian Vanhove
Filip De Vos
Stefaan Vandenberghe
Steven Staelens
author_facet Bert Vandeghinste
Roel Van Holen
Christian Vanhove
Filip De Vos
Stefaan Vandenberghe
Steven Staelens
author_sort Bert Vandeghinste
collection DOAJ
description This work aimed to measure the in vivo quantification errors obtained when ray-based iterative reconstruction is used in micro-single-photon emission computed tomography (SPECT). This was investigated with an extensive phantom-based evaluation and two typical in vivo studies using 99m Tc and 111 In, measured on a commercially available cadmium zinc telluride (CZT)-based small-animal scanner. Iterative reconstruction was implemented on the GPU using ray tracing, including (1) scatter correction, (2) computed tomography-based attenuation correction, (3) resolution recovery, and (4) edge-preserving smoothing. It was validated using a National Electrical Manufacturers Association (NEMA) phantom. The in vivo quantification error was determined for two radiotracers: [ 99m Tc]DMSA in naive mice ( n = 10 kidneys) and [ 111 In]octreotide in mice ( n = 6) inoculated with a xenograft neuroendocrine tumor (NCI-H727). The measured energy resolution is 5.3% for 140.51 keV ( 99m Tc), 4.8% for 171.30 keV, and 3.3% for 245.39 keV ( 111 In). For 99m Tc, an uncorrected quantification error of 28 ± 3% is reduced to 8 ± 3%. For 111 In, the error reduces from 26 ± 14% to 6 ± 22%. The in vivo error obtained with “ m Tc-dimercaptosuccinic acid ([ 99m Tc]DMSA) is reduced from 16.2 ± 2.8% to −0.3 ± 2.1% and from 16.7 ± 10.1% to 2.2 ± 10.6% with [ 111 In]octreotide. Absolute quantitative in vivo SPECT is possible without explicit system matrix measurements. An absolute in vivo quantification error smaller than 5% was achieved and exemplified for both [” m Tc]DMSA and [ 111 In]octreotide.
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spelling doaj.art-e0340e8896ff42748c7a1cdeb6990fd62025-01-03T00:12:14ZengSAGE PublishingMolecular Imaging1536-01212014-06-011310.2310/7290.2014.0000710.2310_7290.2014.00007Use of a Ray-Based Reconstruction Algorithm to Accurately Quantify Preclinical MicroSPECT ImagesBert VandeghinsteRoel Van HolenChristian VanhoveFilip De VosStefaan VandenbergheSteven StaelensThis work aimed to measure the in vivo quantification errors obtained when ray-based iterative reconstruction is used in micro-single-photon emission computed tomography (SPECT). This was investigated with an extensive phantom-based evaluation and two typical in vivo studies using 99m Tc and 111 In, measured on a commercially available cadmium zinc telluride (CZT)-based small-animal scanner. Iterative reconstruction was implemented on the GPU using ray tracing, including (1) scatter correction, (2) computed tomography-based attenuation correction, (3) resolution recovery, and (4) edge-preserving smoothing. It was validated using a National Electrical Manufacturers Association (NEMA) phantom. The in vivo quantification error was determined for two radiotracers: [ 99m Tc]DMSA in naive mice ( n = 10 kidneys) and [ 111 In]octreotide in mice ( n = 6) inoculated with a xenograft neuroendocrine tumor (NCI-H727). The measured energy resolution is 5.3% for 140.51 keV ( 99m Tc), 4.8% for 171.30 keV, and 3.3% for 245.39 keV ( 111 In). For 99m Tc, an uncorrected quantification error of 28 ± 3% is reduced to 8 ± 3%. For 111 In, the error reduces from 26 ± 14% to 6 ± 22%. The in vivo error obtained with “ m Tc-dimercaptosuccinic acid ([ 99m Tc]DMSA) is reduced from 16.2 ± 2.8% to −0.3 ± 2.1% and from 16.7 ± 10.1% to 2.2 ± 10.6% with [ 111 In]octreotide. Absolute quantitative in vivo SPECT is possible without explicit system matrix measurements. An absolute in vivo quantification error smaller than 5% was achieved and exemplified for both [” m Tc]DMSA and [ 111 In]octreotide.https://doi.org/10.2310/7290.2014.00007
spellingShingle Bert Vandeghinste
Roel Van Holen
Christian Vanhove
Filip De Vos
Stefaan Vandenberghe
Steven Staelens
Use of a Ray-Based Reconstruction Algorithm to Accurately Quantify Preclinical MicroSPECT Images
Molecular Imaging
title Use of a Ray-Based Reconstruction Algorithm to Accurately Quantify Preclinical MicroSPECT Images
title_full Use of a Ray-Based Reconstruction Algorithm to Accurately Quantify Preclinical MicroSPECT Images
title_fullStr Use of a Ray-Based Reconstruction Algorithm to Accurately Quantify Preclinical MicroSPECT Images
title_full_unstemmed Use of a Ray-Based Reconstruction Algorithm to Accurately Quantify Preclinical MicroSPECT Images
title_short Use of a Ray-Based Reconstruction Algorithm to Accurately Quantify Preclinical MicroSPECT Images
title_sort use of a ray based reconstruction algorithm to accurately quantify preclinical microspect images
url https://doi.org/10.2310/7290.2014.00007
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