Cargando…

A strategy to account for noise in the X-variable to reduce underestimation in Logan graphical analysis for quantifying receptor density in positron emission tomography

BACKGROUND: The Logan graphical analysis (LGA) algorithm is widely used to quantify receptor density for parametric imaging in positron emission tomography (PET). Estimating receptor density, in terms of the non-displaceable binding potential (BP(ND)), from the LGA using the ordinary least-squares (...

Descripción completa

Detalles Bibliográficos
Autores principales: Shigwedha, Paulus K., Yamada, Takahiro, Hanaoka, Kohei, Ishii, Kazunari, Kimura, Yuichi, Fukuoka, Yutaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011280/
https://www.ncbi.nlm.nih.gov/pubmed/32041550
http://dx.doi.org/10.1186/s12880-020-0421-6
_version_ 1783496038299992064
author Shigwedha, Paulus K.
Yamada, Takahiro
Hanaoka, Kohei
Ishii, Kazunari
Kimura, Yuichi
Fukuoka, Yutaka
author_facet Shigwedha, Paulus K.
Yamada, Takahiro
Hanaoka, Kohei
Ishii, Kazunari
Kimura, Yuichi
Fukuoka, Yutaka
author_sort Shigwedha, Paulus K.
collection PubMed
description BACKGROUND: The Logan graphical analysis (LGA) algorithm is widely used to quantify receptor density for parametric imaging in positron emission tomography (PET). Estimating receptor density, in terms of the non-displaceable binding potential (BP(ND)), from the LGA using the ordinary least-squares (OLS) method has been found to be negatively biased owing to noise in PET data. This is because OLS does not consider errors in the X-variable (predictor variable). Existing bias reduction methods can either only reduce the bias slightly or reduce the bias accompanied by increased variation in the estimates. In this study, we addressed the bias reduction problem by applying a different regression method. METHODS: We employed least-squares cubic (LSC) linear regression, which accounts for errors in both variables as well as the correlation of these errors. Noise-free PET data were simulated, for (11)C-carfentanil kinetics, with known BP(ND) values. Statistical noise was added to these data and the BP(ND)s were re-estimated from the noisy data by three methods, conventional LGA, multilinear reference tissue model 2 (MRTM2), and LSC-based LGA; the results were compared. The three methods were also compared in terms of beta amyloid (A β) quantification of (11)C-Pittsburgh compound B brain PET data for two patients with Alzheimer’s disease and differing A β depositions. RESULTS: Amongst the three methods, for both synthetic and actual data, LSC was the least biased, followed by MRTM2, and then the conventional LGA, which was the most biased. Variations in the LSC estimates were smaller than those in the MRTM2 estimates. LSC also required a shorter computational time than MRTM2. CONCLUSIONS: The results suggest that LSC provides a better trade-off between the bias and variability than the other two methods. In particular, LSC performed better than MRTM2 in all aspects; bias, variability, and computational time. This makes LSC a promising method for BP(ND) parametric imaging in PET studies.
format Online
Article
Text
id pubmed-7011280
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-70112802020-02-14 A strategy to account for noise in the X-variable to reduce underestimation in Logan graphical analysis for quantifying receptor density in positron emission tomography Shigwedha, Paulus K. Yamada, Takahiro Hanaoka, Kohei Ishii, Kazunari Kimura, Yuichi Fukuoka, Yutaka BMC Med Imaging Research Article BACKGROUND: The Logan graphical analysis (LGA) algorithm is widely used to quantify receptor density for parametric imaging in positron emission tomography (PET). Estimating receptor density, in terms of the non-displaceable binding potential (BP(ND)), from the LGA using the ordinary least-squares (OLS) method has been found to be negatively biased owing to noise in PET data. This is because OLS does not consider errors in the X-variable (predictor variable). Existing bias reduction methods can either only reduce the bias slightly or reduce the bias accompanied by increased variation in the estimates. In this study, we addressed the bias reduction problem by applying a different regression method. METHODS: We employed least-squares cubic (LSC) linear regression, which accounts for errors in both variables as well as the correlation of these errors. Noise-free PET data were simulated, for (11)C-carfentanil kinetics, with known BP(ND) values. Statistical noise was added to these data and the BP(ND)s were re-estimated from the noisy data by three methods, conventional LGA, multilinear reference tissue model 2 (MRTM2), and LSC-based LGA; the results were compared. The three methods were also compared in terms of beta amyloid (A β) quantification of (11)C-Pittsburgh compound B brain PET data for two patients with Alzheimer’s disease and differing A β depositions. RESULTS: Amongst the three methods, for both synthetic and actual data, LSC was the least biased, followed by MRTM2, and then the conventional LGA, which was the most biased. Variations in the LSC estimates were smaller than those in the MRTM2 estimates. LSC also required a shorter computational time than MRTM2. CONCLUSIONS: The results suggest that LSC provides a better trade-off between the bias and variability than the other two methods. In particular, LSC performed better than MRTM2 in all aspects; bias, variability, and computational time. This makes LSC a promising method for BP(ND) parametric imaging in PET studies. BioMed Central 2020-02-10 /pmc/articles/PMC7011280/ /pubmed/32041550 http://dx.doi.org/10.1186/s12880-020-0421-6 Text en © The Author(s) 2020 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.
spellingShingle Research Article
Shigwedha, Paulus K.
Yamada, Takahiro
Hanaoka, Kohei
Ishii, Kazunari
Kimura, Yuichi
Fukuoka, Yutaka
A strategy to account for noise in the X-variable to reduce underestimation in Logan graphical analysis for quantifying receptor density in positron emission tomography
title A strategy to account for noise in the X-variable to reduce underestimation in Logan graphical analysis for quantifying receptor density in positron emission tomography
title_full A strategy to account for noise in the X-variable to reduce underestimation in Logan graphical analysis for quantifying receptor density in positron emission tomography
title_fullStr A strategy to account for noise in the X-variable to reduce underestimation in Logan graphical analysis for quantifying receptor density in positron emission tomography
title_full_unstemmed A strategy to account for noise in the X-variable to reduce underestimation in Logan graphical analysis for quantifying receptor density in positron emission tomography
title_short A strategy to account for noise in the X-variable to reduce underestimation in Logan graphical analysis for quantifying receptor density in positron emission tomography
title_sort strategy to account for noise in the x-variable to reduce underestimation in logan graphical analysis for quantifying receptor density in positron emission tomography
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7011280/
https://www.ncbi.nlm.nih.gov/pubmed/32041550
http://dx.doi.org/10.1186/s12880-020-0421-6
work_keys_str_mv AT shigwedhapaulusk astrategytoaccountfornoiseinthexvariabletoreduceunderestimationinlogangraphicalanalysisforquantifyingreceptordensityinpositronemissiontomography
AT yamadatakahiro astrategytoaccountfornoiseinthexvariabletoreduceunderestimationinlogangraphicalanalysisforquantifyingreceptordensityinpositronemissiontomography
AT hanaokakohei astrategytoaccountfornoiseinthexvariabletoreduceunderestimationinlogangraphicalanalysisforquantifyingreceptordensityinpositronemissiontomography
AT ishiikazunari astrategytoaccountfornoiseinthexvariabletoreduceunderestimationinlogangraphicalanalysisforquantifyingreceptordensityinpositronemissiontomography
AT kimurayuichi astrategytoaccountfornoiseinthexvariabletoreduceunderestimationinlogangraphicalanalysisforquantifyingreceptordensityinpositronemissiontomography
AT fukuokayutaka astrategytoaccountfornoiseinthexvariabletoreduceunderestimationinlogangraphicalanalysisforquantifyingreceptordensityinpositronemissiontomography
AT shigwedhapaulusk strategytoaccountfornoiseinthexvariabletoreduceunderestimationinlogangraphicalanalysisforquantifyingreceptordensityinpositronemissiontomography
AT yamadatakahiro strategytoaccountfornoiseinthexvariabletoreduceunderestimationinlogangraphicalanalysisforquantifyingreceptordensityinpositronemissiontomography
AT hanaokakohei strategytoaccountfornoiseinthexvariabletoreduceunderestimationinlogangraphicalanalysisforquantifyingreceptordensityinpositronemissiontomography
AT ishiikazunari strategytoaccountfornoiseinthexvariabletoreduceunderestimationinlogangraphicalanalysisforquantifyingreceptordensityinpositronemissiontomography
AT kimurayuichi strategytoaccountfornoiseinthexvariabletoreduceunderestimationinlogangraphicalanalysisforquantifyingreceptordensityinpositronemissiontomography
AT fukuokayutaka strategytoaccountfornoiseinthexvariabletoreduceunderestimationinlogangraphicalanalysisforquantifyingreceptordensityinpositronemissiontomography