Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Kodal, Jakob B., Vedel-Krogh, Signe, Kobylecki, Camilla J., Nordestgaard, Børge G., Bojesen, Stig E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
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
_version_ 1783235822662713344
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
work_keys_str_mv AT kodaljakobb tp53arg72promortalityaftercancerandallcausemortalityin105200individuals
AT vedelkroghsigne tp53arg72promortalityaftercancerandallcausemortalityin105200individuals
AT kobyleckicamillaj tp53arg72promortalityaftercancerandallcausemortalityin105200individuals
AT nordestgaardbørgeg tp53arg72promortalityaftercancerandallcausemortalityin105200individuals
AT bojesenstige tp53arg72promortalityaftercancerandallcausemortalityin105200individuals