Assessing the effect of treatment duration on the association between anti-diabetic medication and cancer risk.

Most studies that have evaluated the association between anti-diabetic medication and cancer risk have suffered from methodological drawbacks. To avoid time-related biases, we evaluated the effect of treatment duration on the cancer risk among naive users of anti-diabetic medication as compared to n...

Full description

Bibliographic Details
Main Authors: Anna But, Haining Wang, Satu Männistö, Eero Pukkala, Jari Haukka
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4242520?pdf=render
id doaj-1b0aa88d279d441ea2b44090b05df024
record_format Article
spelling doaj-1b0aa88d279d441ea2b44090b05df0242020-11-25T02:33:30ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01911e11316210.1371/journal.pone.0113162Assessing the effect of treatment duration on the association between anti-diabetic medication and cancer risk.Anna ButHaining WangSatu MännistöEero PukkalaJari HaukkaMost studies that have evaluated the association between anti-diabetic medication and cancer risk have suffered from methodological drawbacks. To avoid time-related biases, we evaluated the effect of treatment duration on the cancer risk among naive users of anti-diabetic medication as compared to non-users. In addition, we addressed the influence of common risk factors such as smoking and BMI. The study population comprised 23,394 participants of FINRISK surveys. Data on cancer and anti-diabetic medication were linked with the study cohorts. We applied Lexis tabulation to the data and analyzed split records by using Poisson regression. Changes in cancer incidence in relation to treatment duration were examined by modeling the rate ratio (RR). After a median follow-up of 9 years, 53 cancer cases among users of anti-diabetic medication and 1,028 among non-users were diagnosed. No significant difference in cancer risk between users and non-users was observed after adjustment. The RR for all medication regardless of its duration was 1.01 [95% CI 0.75-1.33], and 1.37 [0.94-1.94] for period of 1-4 years. The results were similar for metformin, sulfonylurea, and insulin. This study demonstrates that evaluation of the variation in cancer risk in relation to treatment duration is of particular importance for enhancing the accuracy of conclusions on the link between exposure to anti-diabetic medication and cancer risk.http://europepmc.org/articles/PMC4242520?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Anna But
Haining Wang
Satu Männistö
Eero Pukkala
Jari Haukka
spellingShingle Anna But
Haining Wang
Satu Männistö
Eero Pukkala
Jari Haukka
Assessing the effect of treatment duration on the association between anti-diabetic medication and cancer risk.
PLoS ONE
author_facet Anna But
Haining Wang
Satu Männistö
Eero Pukkala
Jari Haukka
author_sort Anna But
title Assessing the effect of treatment duration on the association between anti-diabetic medication and cancer risk.
title_short Assessing the effect of treatment duration on the association between anti-diabetic medication and cancer risk.
title_full Assessing the effect of treatment duration on the association between anti-diabetic medication and cancer risk.
title_fullStr Assessing the effect of treatment duration on the association between anti-diabetic medication and cancer risk.
title_full_unstemmed Assessing the effect of treatment duration on the association between anti-diabetic medication and cancer risk.
title_sort assessing the effect of treatment duration on the association between anti-diabetic medication and cancer risk.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Most studies that have evaluated the association between anti-diabetic medication and cancer risk have suffered from methodological drawbacks. To avoid time-related biases, we evaluated the effect of treatment duration on the cancer risk among naive users of anti-diabetic medication as compared to non-users. In addition, we addressed the influence of common risk factors such as smoking and BMI. The study population comprised 23,394 participants of FINRISK surveys. Data on cancer and anti-diabetic medication were linked with the study cohorts. We applied Lexis tabulation to the data and analyzed split records by using Poisson regression. Changes in cancer incidence in relation to treatment duration were examined by modeling the rate ratio (RR). After a median follow-up of 9 years, 53 cancer cases among users of anti-diabetic medication and 1,028 among non-users were diagnosed. No significant difference in cancer risk between users and non-users was observed after adjustment. The RR for all medication regardless of its duration was 1.01 [95% CI 0.75-1.33], and 1.37 [0.94-1.94] for period of 1-4 years. The results were similar for metformin, sulfonylurea, and insulin. This study demonstrates that evaluation of the variation in cancer risk in relation to treatment duration is of particular importance for enhancing the accuracy of conclusions on the link between exposure to anti-diabetic medication and cancer risk.
url http://europepmc.org/articles/PMC4242520?pdf=render
work_keys_str_mv AT annabut assessingtheeffectoftreatmentdurationontheassociationbetweenantidiabeticmedicationandcancerrisk
AT hainingwang assessingtheeffectoftreatmentdurationontheassociationbetweenantidiabeticmedicationandcancerrisk
AT satumannisto assessingtheeffectoftreatmentdurationontheassociationbetweenantidiabeticmedicationandcancerrisk
AT eeropukkala assessingtheeffectoftreatmentdurationontheassociationbetweenantidiabeticmedicationandcancerrisk
AT jarihaukka assessingtheeffectoftreatmentdurationontheassociationbetweenantidiabeticmedicationandcancerrisk
_version_ 1724813678449000448