A machine learning method for improving the accuracy of radiation biodosimetry by combining data from the dicentric chromosomes and micronucleus assays

Abstract A large-scale malicious or accidental radiological event can expose vast numbers of people to ionizing radiation. The dicentric chromosome (DCA) and cytokinesis-block micronucleus (CBMN) assays are well-established biodosimetry methods for estimating individual absorbed doses after radiatio...

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Main Authors: Igor Shuryak, Ekaterina Royba, Mikhail Repin, Helen C. Turner, Guy Garty, Naresh Deoli, David J. Brenner
Format: Article
Language:English
Published: Nature Portfolio 2022-12-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-022-25453-2
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author Igor Shuryak
Ekaterina Royba
Mikhail Repin
Helen C. Turner
Guy Garty
Naresh Deoli
David J. Brenner
author_facet Igor Shuryak
Ekaterina Royba
Mikhail Repin
Helen C. Turner
Guy Garty
Naresh Deoli
David J. Brenner
author_sort Igor Shuryak
collection DOAJ
description Abstract A large-scale malicious or accidental radiological event can expose vast numbers of people to ionizing radiation. The dicentric chromosome (DCA) and cytokinesis-block micronucleus (CBMN) assays are well-established biodosimetry methods for estimating individual absorbed doses after radiation exposure. Here we used machine learning (ML) to test the hypothesis that combining automated DCA and CBMN assays will improve dose reconstruction accuracy, compared with using either cytogenetic assay alone. We analyzed 1349 blood sample aliquots from 155 donors of different ages (3–69 years) and sexes (49.1% males), ex vivo irradiated with 0–8 Gy at dose rates from 0.08 Gy/day to ≥ 600 Gy/s. We compared the performances of several state-of-the-art ensemble ML methods and found that random forest generated the best results, with R2 for actual vs. reconstructed doses on a testing data subset = 0.845, and mean absolute error = 0.628 Gy. The most important predictor variables were CBMN and DCA frequencies, and age. Removing CBMN or DCA data from the model significantly increased squared errors on testing data (p-values 3.4 × 10–8 and 1.1 × 10–6, respectively). These findings demonstrate the promising potential of combining CBMN and DCA assay data to reconstruct radiation doses in realistic scenarios of heterogeneous populations exposed to a mass-casualty radiological event.
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spelling doaj.art-1a15af263c514e6d8d0c2477e6a4ca662022-12-22T04:18:47ZengNature PortfolioScientific Reports2045-23222022-12-0112111310.1038/s41598-022-25453-2A machine learning method for improving the accuracy of radiation biodosimetry by combining data from the dicentric chromosomes and micronucleus assaysIgor Shuryak0Ekaterina Royba1Mikhail Repin2Helen C. Turner3Guy Garty4Naresh Deoli5David J. Brenner6Center for Radiological Research, Columbia University Irving Medical CenterCenter for Radiological Research, Columbia University Irving Medical CenterCenter for Radiological Research, Columbia University Irving Medical CenterCenter for Radiological Research, Columbia University Irving Medical CenterRadiological Research Accelerator Facility, Columbia University Irving Medical CenterRadiological Research Accelerator Facility, Columbia University Irving Medical CenterCenter for Radiological Research, Columbia University Irving Medical CenterAbstract A large-scale malicious or accidental radiological event can expose vast numbers of people to ionizing radiation. The dicentric chromosome (DCA) and cytokinesis-block micronucleus (CBMN) assays are well-established biodosimetry methods for estimating individual absorbed doses after radiation exposure. Here we used machine learning (ML) to test the hypothesis that combining automated DCA and CBMN assays will improve dose reconstruction accuracy, compared with using either cytogenetic assay alone. We analyzed 1349 blood sample aliquots from 155 donors of different ages (3–69 years) and sexes (49.1% males), ex vivo irradiated with 0–8 Gy at dose rates from 0.08 Gy/day to ≥ 600 Gy/s. We compared the performances of several state-of-the-art ensemble ML methods and found that random forest generated the best results, with R2 for actual vs. reconstructed doses on a testing data subset = 0.845, and mean absolute error = 0.628 Gy. The most important predictor variables were CBMN and DCA frequencies, and age. Removing CBMN or DCA data from the model significantly increased squared errors on testing data (p-values 3.4 × 10–8 and 1.1 × 10–6, respectively). These findings demonstrate the promising potential of combining CBMN and DCA assay data to reconstruct radiation doses in realistic scenarios of heterogeneous populations exposed to a mass-casualty radiological event.https://doi.org/10.1038/s41598-022-25453-2
spellingShingle Igor Shuryak
Ekaterina Royba
Mikhail Repin
Helen C. Turner
Guy Garty
Naresh Deoli
David J. Brenner
A machine learning method for improving the accuracy of radiation biodosimetry by combining data from the dicentric chromosomes and micronucleus assays
Scientific Reports
title A machine learning method for improving the accuracy of radiation biodosimetry by combining data from the dicentric chromosomes and micronucleus assays
title_full A machine learning method for improving the accuracy of radiation biodosimetry by combining data from the dicentric chromosomes and micronucleus assays
title_fullStr A machine learning method for improving the accuracy of radiation biodosimetry by combining data from the dicentric chromosomes and micronucleus assays
title_full_unstemmed A machine learning method for improving the accuracy of radiation biodosimetry by combining data from the dicentric chromosomes and micronucleus assays
title_short A machine learning method for improving the accuracy of radiation biodosimetry by combining data from the dicentric chromosomes and micronucleus assays
title_sort machine learning method for improving the accuracy of radiation biodosimetry by combining data from the dicentric chromosomes and micronucleus assays
url https://doi.org/10.1038/s41598-022-25453-2
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