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TP53 Arg72Pro, mortality after cancer, and all-cause mortality in 105,200 individuals
Rs1042522 (Arg72Pro) is a functional polymorphism of TP53. Pro72 has been associated with lower all-cause mortality and lower mortality after cancer. We hypothesized that TP53 Pro72 is associated with lower mortality after cancer, lower all-cause mortality, and with increased cancer incidence in the...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428447/ https://www.ncbi.nlm.nih.gov/pubmed/28336930 http://dx.doi.org/10.1038/s41598-017-00427-x |
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author | Kodal, Jakob B. Vedel-Krogh, Signe Kobylecki, Camilla J. Nordestgaard, Børge G. Bojesen, Stig E. |
author_facet | Kodal, Jakob B. Vedel-Krogh, Signe Kobylecki, Camilla J. Nordestgaard, Børge G. Bojesen, Stig E. |
author_sort | Kodal, Jakob B. |
collection | PubMed |
description | Rs1042522 (Arg72Pro) is a functional polymorphism of TP53. Pro72 has been associated with lower all-cause mortality and lower mortality after cancer. We hypothesized that TP53 Pro72 is associated with lower mortality after cancer, lower all-cause mortality, and with increased cancer incidence in the general population in a contemporary cohort. We genotyped 105,200 individuals aged 20–100 years from the Copenhagen General Population Study, recruited in 2003–2013, and followed them in Danish health registries. During follow-up 5,531 individuals died and 5,849 developed cancer. Hazard ratios for mortality after cancer were 1.03 (95% confidence interval:0.93–1.15) for Arg/Pro and 0.96 (95% CI:0.79–1.18) for Pro/Pro versus Arg/Arg. Hazard ratios for all-cause mortality were 0.99 (95% CI:0.93–1.04) for Arg/Pro and 1.09 (95% CI:0.98–1.21) for Pro/Pro versus Arg/Arg. Risk of cancer specific mortality, cardiovascular mortality, and respiratory mortality were not associated with Arg72Pro genotype overall; however, in exploratory subgroup analyses, genotype-associated risks of malignant melanoma and diabetes were altered. Considering multiple comparisons the latter findings may represent play of chance. The TP53 Arg72Pro genotype was not associated with mortality after cancer, all-cause mortality, or cancer incidence in the general population in a contemporary cohort. Our main conclusion is therefore a lack of reproducing an effect of TP53 Arg72Pro genotype on mortality. |
format | Online Article Text |
id | pubmed-5428447 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54284472017-05-15 TP53 Arg72Pro, mortality after cancer, and all-cause mortality in 105,200 individuals Kodal, Jakob B. Vedel-Krogh, Signe Kobylecki, Camilla J. Nordestgaard, Børge G. Bojesen, Stig E. Sci Rep Article Rs1042522 (Arg72Pro) is a functional polymorphism of TP53. Pro72 has been associated with lower all-cause mortality and lower mortality after cancer. We hypothesized that TP53 Pro72 is associated with lower mortality after cancer, lower all-cause mortality, and with increased cancer incidence in the general population in a contemporary cohort. We genotyped 105,200 individuals aged 20–100 years from the Copenhagen General Population Study, recruited in 2003–2013, and followed them in Danish health registries. During follow-up 5,531 individuals died and 5,849 developed cancer. Hazard ratios for mortality after cancer were 1.03 (95% confidence interval:0.93–1.15) for Arg/Pro and 0.96 (95% CI:0.79–1.18) for Pro/Pro versus Arg/Arg. Hazard ratios for all-cause mortality were 0.99 (95% CI:0.93–1.04) for Arg/Pro and 1.09 (95% CI:0.98–1.21) for Pro/Pro versus Arg/Arg. Risk of cancer specific mortality, cardiovascular mortality, and respiratory mortality were not associated with Arg72Pro genotype overall; however, in exploratory subgroup analyses, genotype-associated risks of malignant melanoma and diabetes were altered. Considering multiple comparisons the latter findings may represent play of chance. The TP53 Arg72Pro genotype was not associated with mortality after cancer, all-cause mortality, or cancer incidence in the general population in a contemporary cohort. Our main conclusion is therefore a lack of reproducing an effect of TP53 Arg72Pro genotype on mortality. Nature Publishing Group UK 2017-03-23 /pmc/articles/PMC5428447/ /pubmed/28336930 http://dx.doi.org/10.1038/s41598-017-00427-x Text en © The Author(s) 2017 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Kodal, Jakob B. Vedel-Krogh, Signe Kobylecki, Camilla J. Nordestgaard, Børge G. Bojesen, Stig E. TP53 Arg72Pro, mortality after cancer, and all-cause mortality in 105,200 individuals |
title | TP53 Arg72Pro, mortality after cancer, and all-cause mortality in 105,200 individuals |
title_full | TP53 Arg72Pro, mortality after cancer, and all-cause mortality in 105,200 individuals |
title_fullStr | TP53 Arg72Pro, mortality after cancer, and all-cause mortality in 105,200 individuals |
title_full_unstemmed | TP53 Arg72Pro, mortality after cancer, and all-cause mortality in 105,200 individuals |
title_short | TP53 Arg72Pro, mortality after cancer, and all-cause mortality in 105,200 individuals |
title_sort | tp53 arg72pro, mortality after cancer, and all-cause mortality in 105,200 individuals |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428447/ https://www.ncbi.nlm.nih.gov/pubmed/28336930 http://dx.doi.org/10.1038/s41598-017-00427-x |
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