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Colorectal cancer, comorbidity, and risk of venous thromboembolism: assessment of biological interactions in a Danish nationwide cohort
BACKGROUND: Venous thromboembolism (VTE) is a major source of morbidity and mortality in cancer patients. Incident colorectal cancer (CRC) and comorbidity both predict VTE, but potential synergy between these factors has not been explored. METHODS: Danish nationwide cohort study of CRC cases diagnos...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2016
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4716535/ https://www.ncbi.nlm.nih.gov/pubmed/26625005 http://dx.doi.org/10.1038/bjc.2015.406 |
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author | Ahern, Thomas P Horváth-Puhó, Erzsébet Spindler, Karen-Lise Garm Sørensen, Henrik Toft Ording, Anne G Erichsen, Rune |
author_facet | Ahern, Thomas P Horváth-Puhó, Erzsébet Spindler, Karen-Lise Garm Sørensen, Henrik Toft Ording, Anne G Erichsen, Rune |
author_sort | Ahern, Thomas P |
collection | PubMed |
description | BACKGROUND: Venous thromboembolism (VTE) is a major source of morbidity and mortality in cancer patients. Incident colorectal cancer (CRC) and comorbidity both predict VTE, but potential synergy between these factors has not been explored. METHODS: Danish nationwide cohort study of CRC cases diagnosed in 1995–2010 and a matched general population reference cohort of subjects without CRC who matched cases on age, sex, and comorbidities. We calculated the Charlson Comorbidity Index using diagnoses recorded in the Danish National Patient Registry. We calculated standardised incidence rates (SIRs) and interaction contrasts (IC) to measure additive interaction between comorbidity and CRC status with respect to 5-year VTE incidence. RESULTS: Among 56 189 CRC patients, 1372 VTE cases were diagnosed over 145 211 person-years (SIR=9.5 cases per 1000 person-years). Among 271 670 reference subjects, 2867 VTE cases were diagnosed over 1 068 860 person-years (SIR=2.8 cases per 1000 person-years). CRC and comorbidity were positively and independently associated with VTE, but there was no evidence for biological interaction between these factors (e.g., comparing the ‘severe comorbidity' stratum with the ‘no comorbidity' stratum, IC=0.8, 95% CI: −3.3, 4.8). CONCLUSIONS: There is neither a deficit nor a surplus of VTE cases among patients with both comorbidity and CRC, compared with rates expected from these risk factors in isolation. |
format | Online Article Text |
id | pubmed-4716535 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-47165352017-01-12 Colorectal cancer, comorbidity, and risk of venous thromboembolism: assessment of biological interactions in a Danish nationwide cohort Ahern, Thomas P Horváth-Puhó, Erzsébet Spindler, Karen-Lise Garm Sørensen, Henrik Toft Ording, Anne G Erichsen, Rune Br J Cancer Epidemiology BACKGROUND: Venous thromboembolism (VTE) is a major source of morbidity and mortality in cancer patients. Incident colorectal cancer (CRC) and comorbidity both predict VTE, but potential synergy between these factors has not been explored. METHODS: Danish nationwide cohort study of CRC cases diagnosed in 1995–2010 and a matched general population reference cohort of subjects without CRC who matched cases on age, sex, and comorbidities. We calculated the Charlson Comorbidity Index using diagnoses recorded in the Danish National Patient Registry. We calculated standardised incidence rates (SIRs) and interaction contrasts (IC) to measure additive interaction between comorbidity and CRC status with respect to 5-year VTE incidence. RESULTS: Among 56 189 CRC patients, 1372 VTE cases were diagnosed over 145 211 person-years (SIR=9.5 cases per 1000 person-years). Among 271 670 reference subjects, 2867 VTE cases were diagnosed over 1 068 860 person-years (SIR=2.8 cases per 1000 person-years). CRC and comorbidity were positively and independently associated with VTE, but there was no evidence for biological interaction between these factors (e.g., comparing the ‘severe comorbidity' stratum with the ‘no comorbidity' stratum, IC=0.8, 95% CI: −3.3, 4.8). CONCLUSIONS: There is neither a deficit nor a surplus of VTE cases among patients with both comorbidity and CRC, compared with rates expected from these risk factors in isolation. Nature Publishing Group 2016-01-12 2015-12-01 /pmc/articles/PMC4716535/ /pubmed/26625005 http://dx.doi.org/10.1038/bjc.2015.406 Text en Copyright © 2016 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Epidemiology Ahern, Thomas P Horváth-Puhó, Erzsébet Spindler, Karen-Lise Garm Sørensen, Henrik Toft Ording, Anne G Erichsen, Rune Colorectal cancer, comorbidity, and risk of venous thromboembolism: assessment of biological interactions in a Danish nationwide cohort |
title | Colorectal cancer, comorbidity, and risk of venous thromboembolism: assessment of biological interactions in a Danish nationwide cohort |
title_full | Colorectal cancer, comorbidity, and risk of venous thromboembolism: assessment of biological interactions in a Danish nationwide cohort |
title_fullStr | Colorectal cancer, comorbidity, and risk of venous thromboembolism: assessment of biological interactions in a Danish nationwide cohort |
title_full_unstemmed | Colorectal cancer, comorbidity, and risk of venous thromboembolism: assessment of biological interactions in a Danish nationwide cohort |
title_short | Colorectal cancer, comorbidity, and risk of venous thromboembolism: assessment of biological interactions in a Danish nationwide cohort |
title_sort | colorectal cancer, comorbidity, and risk of venous thromboembolism: assessment of biological interactions in a danish nationwide cohort |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4716535/ https://www.ncbi.nlm.nih.gov/pubmed/26625005 http://dx.doi.org/10.1038/bjc.2015.406 |
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