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Risk of bladder cancer in patients with diabetes: a retrospective cohort study
OBJECTIVE: The objective of this study was to examine the association between diabetes, and both urinary bladder cancer (UBC) risk and mortality. METHODS: We conducted a retrospective cohort study using data from the UK Clinical Practice Research Datalink (CPRD) linked to the Office of National Stat...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458630/ https://www.ncbi.nlm.nih.gov/pubmed/26033947 http://dx.doi.org/10.1136/bmjopen-2014-007470 |
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author | Goossens, Maria E Zeegers, Maurice P Bazelier, Marloes T De Bruin, Marie L Buntinx, Frank de Vries, Frank |
author_facet | Goossens, Maria E Zeegers, Maurice P Bazelier, Marloes T De Bruin, Marie L Buntinx, Frank de Vries, Frank |
author_sort | Goossens, Maria E |
collection | PubMed |
description | OBJECTIVE: The objective of this study was to examine the association between diabetes, and both urinary bladder cancer (UBC) risk and mortality. METHODS: We conducted a retrospective cohort study using data from the UK Clinical Practice Research Datalink (CPRD) linked to the Office of National Statistics (ONS). Patients diagnosed with diabetes mellitus type 1 or 2, or using antidiabetic drugs (ADDs), were compared to matched non-diabetic controls. Cox proportional hazards models were used to estimate the risk and mortality of UBC. We adjusted for age, sex, smoking status and body mass index. RESULTS: The cohort included 329 168 patients using ADD, and 307 315 controls with 1295 and 1071 patients, respectively, diagnosed as having UBC during follow-up. The adjusted HRs of UBC were 0.77 (95% CI 0.57 to 1.05) and 1.04 (95% CI 0.96 to 1.14) for type 1 and 2 diabetes, respectively. These results were similar if we restricted our analysis to an inception cohort. We noticed a small increased risk during the first year after diagnosis (HR=1.26 (95% CI 1.05 to 1.52)), which could be explained by detection bias. There was no influence of the severity of diabetes as measured by the glycated haemoglobin. Mortality of UBC was not increased for patients with either type 1 (HR=0.95 (95% CI 0.39 to 2.34)) or type 2 diabetes (HR=1.16 (95% CI 0.91 to 1.46)). CONCLUSIONS: Neither the risk of UBC nor the mortality from UBC was increased in patients with type 1 and patients with type 2 diabetes in the CPRD data. |
format | Online Article Text |
id | pubmed-4458630 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-44586302015-06-10 Risk of bladder cancer in patients with diabetes: a retrospective cohort study Goossens, Maria E Zeegers, Maurice P Bazelier, Marloes T De Bruin, Marie L Buntinx, Frank de Vries, Frank BMJ Open Epidemiology OBJECTIVE: The objective of this study was to examine the association between diabetes, and both urinary bladder cancer (UBC) risk and mortality. METHODS: We conducted a retrospective cohort study using data from the UK Clinical Practice Research Datalink (CPRD) linked to the Office of National Statistics (ONS). Patients diagnosed with diabetes mellitus type 1 or 2, or using antidiabetic drugs (ADDs), were compared to matched non-diabetic controls. Cox proportional hazards models were used to estimate the risk and mortality of UBC. We adjusted for age, sex, smoking status and body mass index. RESULTS: The cohort included 329 168 patients using ADD, and 307 315 controls with 1295 and 1071 patients, respectively, diagnosed as having UBC during follow-up. The adjusted HRs of UBC were 0.77 (95% CI 0.57 to 1.05) and 1.04 (95% CI 0.96 to 1.14) for type 1 and 2 diabetes, respectively. These results were similar if we restricted our analysis to an inception cohort. We noticed a small increased risk during the first year after diagnosis (HR=1.26 (95% CI 1.05 to 1.52)), which could be explained by detection bias. There was no influence of the severity of diabetes as measured by the glycated haemoglobin. Mortality of UBC was not increased for patients with either type 1 (HR=0.95 (95% CI 0.39 to 2.34)) or type 2 diabetes (HR=1.16 (95% CI 0.91 to 1.46)). CONCLUSIONS: Neither the risk of UBC nor the mortality from UBC was increased in patients with type 1 and patients with type 2 diabetes in the CPRD data. BMJ Publishing Group 2015-05-30 /pmc/articles/PMC4458630/ /pubmed/26033947 http://dx.doi.org/10.1136/bmjopen-2014-007470 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ |
spellingShingle | Epidemiology Goossens, Maria E Zeegers, Maurice P Bazelier, Marloes T De Bruin, Marie L Buntinx, Frank de Vries, Frank Risk of bladder cancer in patients with diabetes: a retrospective cohort study |
title | Risk of bladder cancer in patients with diabetes: a retrospective cohort study |
title_full | Risk of bladder cancer in patients with diabetes: a retrospective cohort study |
title_fullStr | Risk of bladder cancer in patients with diabetes: a retrospective cohort study |
title_full_unstemmed | Risk of bladder cancer in patients with diabetes: a retrospective cohort study |
title_short | Risk of bladder cancer in patients with diabetes: a retrospective cohort study |
title_sort | risk of bladder cancer in patients with diabetes: a retrospective cohort study |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458630/ https://www.ncbi.nlm.nih.gov/pubmed/26033947 http://dx.doi.org/10.1136/bmjopen-2014-007470 |
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