DNA damage in circulating leukocytes measured with the comet assay may predict the risk of death
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://hdl.handle.net/10216/149492 |
Resumo: | The comet assay or single cell gel electrophoresis, is the most common method used to measure strand breaks and a variety of other DNA lesions in human populations. To estimate the risk of overall mortality, mortality by cause, and cancer incidence associated to DNA damage, a cohort of 2,403 healthy individuals (25,978 person-years) screened in 16 laboratories using the comet assay between 1996 and 2016 was followed-up. Kaplan-Meier analysis indicated a worse overall survival in the medium and high tertile of DNA damage (p < 0.001). The effect of DNA damage on survival was modelled according to Cox proportional hazard regression model. The adjusted hazard ratio (HR) was 1.42 (1.06-1.90) for overall mortality, and 1.94 (1.04-3.59) for diseases of the circulatory system in subjects with the highest tertile of DNA damage. The findings of this study provide epidemiological evidence encouraging the implementation of the comet assay in preventive strategies for non-communicable diseases. Correction: https://doi.org/10.1038/s41598-021-98620-6 |
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DNA damage in circulating leukocytes measured with the comet assay may predict the risk of deathThe comet assay or single cell gel electrophoresis, is the most common method used to measure strand breaks and a variety of other DNA lesions in human populations. To estimate the risk of overall mortality, mortality by cause, and cancer incidence associated to DNA damage, a cohort of 2,403 healthy individuals (25,978 person-years) screened in 16 laboratories using the comet assay between 1996 and 2016 was followed-up. Kaplan-Meier analysis indicated a worse overall survival in the medium and high tertile of DNA damage (p < 0.001). The effect of DNA damage on survival was modelled according to Cox proportional hazard regression model. The adjusted hazard ratio (HR) was 1.42 (1.06-1.90) for overall mortality, and 1.94 (1.04-3.59) for diseases of the circulatory system in subjects with the highest tertile of DNA damage. The findings of this study provide epidemiological evidence encouraging the implementation of the comet assay in preventive strategies for non-communicable diseases. Correction: https://doi.org/10.1038/s41598-021-98620-6Nature Research20212021-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/149492eng2045-232210.1038/s41598-021-95976-7Bonassi, SCeppi, MMøller, PAzqueta, AMilić, MNeri, MBrunborg, GGodschalk, RKoppen, GLangie, SASTeixeira, JPBruzzone, MDa Silva, JBenedetti, DCavallo, DUrsini, CLGiovannelli, LMoretti, SRiso, PDel Bo', CRusso, PDobrzyńska, MGoroshinskaya, IASurikova, EIStaruchova, MBarančokova, MVolkovova, KKažimirova, ASmolkova, BLaffon, BValdiglesias, VPastor, SMarcos, RHernández, AGajski, GSpremo-Potparević, BŽivković, LBoutet-Robinet, EPerdry, HLebailly, PPerez, CLBasaran, NNemeth, ZSafar, ADusinska, MCollins, AhCOMET projectinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-29T15:23:39Zoai:repositorio-aberto.up.pt:10216/149492Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T00:22:32.038822Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
DNA damage in circulating leukocytes measured with the comet assay may predict the risk of death |
title |
DNA damage in circulating leukocytes measured with the comet assay may predict the risk of death |
spellingShingle |
DNA damage in circulating leukocytes measured with the comet assay may predict the risk of death Bonassi, S |
title_short |
DNA damage in circulating leukocytes measured with the comet assay may predict the risk of death |
title_full |
DNA damage in circulating leukocytes measured with the comet assay may predict the risk of death |
title_fullStr |
DNA damage in circulating leukocytes measured with the comet assay may predict the risk of death |
title_full_unstemmed |
DNA damage in circulating leukocytes measured with the comet assay may predict the risk of death |
title_sort |
DNA damage in circulating leukocytes measured with the comet assay may predict the risk of death |
author |
Bonassi, S |
author_facet |
Bonassi, S Ceppi, M Møller, P Azqueta, A Milić, M Neri, M Brunborg, G Godschalk, R Koppen, G Langie, SAS Teixeira, JP Bruzzone, M Da Silva, J Benedetti, D Cavallo, D Ursini, CL Giovannelli, L Moretti, S Riso, P Del Bo', C Russo, P Dobrzyńska, M Goroshinskaya, IA Surikova, EI Staruchova, M Barančokova, M Volkovova, K Kažimirova, A Smolkova, B Laffon, B Valdiglesias, V Pastor, S Marcos, R Hernández, A Gajski, G Spremo-Potparević, B Živković, L Boutet-Robinet, E Perdry, H Lebailly, P Perez, CL Basaran, N Nemeth, Z Safar, A Dusinska, M Collins, A hCOMET project |
author_role |
author |
author2 |
Ceppi, M Møller, P Azqueta, A Milić, M Neri, M Brunborg, G Godschalk, R Koppen, G Langie, SAS Teixeira, JP Bruzzone, M Da Silva, J Benedetti, D Cavallo, D Ursini, CL Giovannelli, L Moretti, S Riso, P Del Bo', C Russo, P Dobrzyńska, M Goroshinskaya, IA Surikova, EI Staruchova, M Barančokova, M Volkovova, K Kažimirova, A Smolkova, B Laffon, B Valdiglesias, V Pastor, S Marcos, R Hernández, A Gajski, G Spremo-Potparević, B Živković, L Boutet-Robinet, E Perdry, H Lebailly, P Perez, CL Basaran, N Nemeth, Z Safar, A Dusinska, M Collins, A hCOMET project |
author2_role |
author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author author |
dc.contributor.author.fl_str_mv |
Bonassi, S Ceppi, M Møller, P Azqueta, A Milić, M Neri, M Brunborg, G Godschalk, R Koppen, G Langie, SAS Teixeira, JP Bruzzone, M Da Silva, J Benedetti, D Cavallo, D Ursini, CL Giovannelli, L Moretti, S Riso, P Del Bo', C Russo, P Dobrzyńska, M Goroshinskaya, IA Surikova, EI Staruchova, M Barančokova, M Volkovova, K Kažimirova, A Smolkova, B Laffon, B Valdiglesias, V Pastor, S Marcos, R Hernández, A Gajski, G Spremo-Potparević, B Živković, L Boutet-Robinet, E Perdry, H Lebailly, P Perez, CL Basaran, N Nemeth, Z Safar, A Dusinska, M Collins, A hCOMET project |
description |
The comet assay or single cell gel electrophoresis, is the most common method used to measure strand breaks and a variety of other DNA lesions in human populations. To estimate the risk of overall mortality, mortality by cause, and cancer incidence associated to DNA damage, a cohort of 2,403 healthy individuals (25,978 person-years) screened in 16 laboratories using the comet assay between 1996 and 2016 was followed-up. Kaplan-Meier analysis indicated a worse overall survival in the medium and high tertile of DNA damage (p < 0.001). The effect of DNA damage on survival was modelled according to Cox proportional hazard regression model. The adjusted hazard ratio (HR) was 1.42 (1.06-1.90) for overall mortality, and 1.94 (1.04-3.59) for diseases of the circulatory system in subjects with the highest tertile of DNA damage. The findings of this study provide epidemiological evidence encouraging the implementation of the comet assay in preventive strategies for non-communicable diseases. Correction: https://doi.org/10.1038/s41598-021-98620-6 |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021 2021-01-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://hdl.handle.net/10216/149492 |
url |
https://hdl.handle.net/10216/149492 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
2045-2322 10.1038/s41598-021-95976-7 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Nature Research |
publisher.none.fl_str_mv |
Nature Research |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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