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Diabetes and cancer risk: A Mendelian randomization study

Earlier cohort studies using conventional regression models have consistently shown an increased cancer risk among individuals with type 2 diabetes. However, reverse causality and residual confounding due to common risk factors could exist, and it remains unclear whether diabetes per se contributes...

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Autores principales: Goto, Atsushi, Yamaji, Taiki, Sawada, Norie, Momozawa, Yukihide, Kamatani, Yoichiro, Kubo, Michiaki, Shimazu, Taichi, Inoue, Manami, Noda, Mitsuhiko, Tsugane, Shoichiro, Iwasaki, Motoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916579/
https://www.ncbi.nlm.nih.gov/pubmed/30927373
http://dx.doi.org/10.1002/ijc.32310
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author Goto, Atsushi
Yamaji, Taiki
Sawada, Norie
Momozawa, Yukihide
Kamatani, Yoichiro
Kubo, Michiaki
Shimazu, Taichi
Inoue, Manami
Noda, Mitsuhiko
Tsugane, Shoichiro
Iwasaki, Motoki
author_facet Goto, Atsushi
Yamaji, Taiki
Sawada, Norie
Momozawa, Yukihide
Kamatani, Yoichiro
Kubo, Michiaki
Shimazu, Taichi
Inoue, Manami
Noda, Mitsuhiko
Tsugane, Shoichiro
Iwasaki, Motoki
author_sort Goto, Atsushi
collection PubMed
description Earlier cohort studies using conventional regression models have consistently shown an increased cancer risk among individuals with type 2 diabetes. However, reverse causality and residual confounding due to common risk factors could exist, and it remains unclear whether diabetes per se contributes to cancer development. Mendelian randomization analyses might clarify the true association between diabetes and cancer risk. We conducted a case–cohort study with 10,536 subcohort subjects and 3,541 newly diagnosed cancer cases derived from 32,949 eligible participants aged 40–69 years within the Japan Public Health Center‐based Prospective Study. With 29 known type 2 diabetes susceptibility variants, we used an inverse variance‐weighted method to estimate hazard ratios for the associations of diabetes with risks of total and site‐specific cancers. The hazard ratios of cancer per doubling of the probability of diabetes were 1.03 (95% confidence interval [CI], 0.92–1.15) overall, 1.08 (95% CI: 0.73–1.59) for the pancreas, 0.80 (95% CI: 0.57–1.14) for the liver and 0.90 (95% CI: 0.74–1.10) for the colorectum. Additional analyses, using publicly available large‐scale genome‐wide association study data on colorectal cancer in Japan, resulted in a narrower CI (hazard ratio: 1.00; 95% CI: 0.93–1.07). In this prospective Mendelian randomization study with a large number of incident cancer cases, we found no strong evidence to support associations between diabetes and overall and site‐specific cancer risks. Our findings suggest that there is little evidence to support the genetic role of type 2 diabetes in cancer development in the Japanese population.
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spelling pubmed-69165792019-12-23 Diabetes and cancer risk: A Mendelian randomization study Goto, Atsushi Yamaji, Taiki Sawada, Norie Momozawa, Yukihide Kamatani, Yoichiro Kubo, Michiaki Shimazu, Taichi Inoue, Manami Noda, Mitsuhiko Tsugane, Shoichiro Iwasaki, Motoki Int J Cancer Cancer Epidemiology Earlier cohort studies using conventional regression models have consistently shown an increased cancer risk among individuals with type 2 diabetes. However, reverse causality and residual confounding due to common risk factors could exist, and it remains unclear whether diabetes per se contributes to cancer development. Mendelian randomization analyses might clarify the true association between diabetes and cancer risk. We conducted a case–cohort study with 10,536 subcohort subjects and 3,541 newly diagnosed cancer cases derived from 32,949 eligible participants aged 40–69 years within the Japan Public Health Center‐based Prospective Study. With 29 known type 2 diabetes susceptibility variants, we used an inverse variance‐weighted method to estimate hazard ratios for the associations of diabetes with risks of total and site‐specific cancers. The hazard ratios of cancer per doubling of the probability of diabetes were 1.03 (95% confidence interval [CI], 0.92–1.15) overall, 1.08 (95% CI: 0.73–1.59) for the pancreas, 0.80 (95% CI: 0.57–1.14) for the liver and 0.90 (95% CI: 0.74–1.10) for the colorectum. Additional analyses, using publicly available large‐scale genome‐wide association study data on colorectal cancer in Japan, resulted in a narrower CI (hazard ratio: 1.00; 95% CI: 0.93–1.07). In this prospective Mendelian randomization study with a large number of incident cancer cases, we found no strong evidence to support associations between diabetes and overall and site‐specific cancer risks. Our findings suggest that there is little evidence to support the genetic role of type 2 diabetes in cancer development in the Japanese population. John Wiley & Sons, Inc. 2019-04-25 2020-02-01 /pmc/articles/PMC6916579/ /pubmed/30927373 http://dx.doi.org/10.1002/ijc.32310 Text en © 2019 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Cancer Epidemiology
Goto, Atsushi
Yamaji, Taiki
Sawada, Norie
Momozawa, Yukihide
Kamatani, Yoichiro
Kubo, Michiaki
Shimazu, Taichi
Inoue, Manami
Noda, Mitsuhiko
Tsugane, Shoichiro
Iwasaki, Motoki
Diabetes and cancer risk: A Mendelian randomization study
title Diabetes and cancer risk: A Mendelian randomization study
title_full Diabetes and cancer risk: A Mendelian randomization study
title_fullStr Diabetes and cancer risk: A Mendelian randomization study
title_full_unstemmed Diabetes and cancer risk: A Mendelian randomization study
title_short Diabetes and cancer risk: A Mendelian randomization study
title_sort diabetes and cancer risk: a mendelian randomization study
topic Cancer Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6916579/
https://www.ncbi.nlm.nih.gov/pubmed/30927373
http://dx.doi.org/10.1002/ijc.32310
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