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Metabolic health is a determining factor for incident colorectal cancer in the obese population: A nationwide population‐based cohort study

BACKGROUND: The association of the risk of colorectal cancer (CRC) with obesity or obesity‐induced metabolic disturbances remains controversial. We assessed the association of metabolic health status with incident CRC among subjects with obesity. METHODS: This study included 319,397 subjects from th...

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Autores principales: Cho, Yun Kyung, Lee, Jiwoo, Kim, Hwi Seung, Park, Joong‐Yeol, Lee, Woo Je, Kim, Ye‐Jee, Jung, Chang Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826459/
https://www.ncbi.nlm.nih.gov/pubmed/33216467
http://dx.doi.org/10.1002/cam4.3607
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author Cho, Yun Kyung
Lee, Jiwoo
Kim, Hwi Seung
Park, Joong‐Yeol
Lee, Woo Je
Kim, Ye‐Jee
Jung, Chang Hee
author_facet Cho, Yun Kyung
Lee, Jiwoo
Kim, Hwi Seung
Park, Joong‐Yeol
Lee, Woo Je
Kim, Ye‐Jee
Jung, Chang Hee
author_sort Cho, Yun Kyung
collection PubMed
description BACKGROUND: The association of the risk of colorectal cancer (CRC) with obesity or obesity‐induced metabolic disturbances remains controversial. We assessed the association of metabolic health status with incident CRC among subjects with obesity. METHODS: This study included 319,397 subjects from the Korean National Health Insurance Service‐National Health Screening Cohort. Transitions in metabolic health status and obesity were examined during 2009–2010 and 2011–2012. We categorized subjects with obesity into four separate groups according to their dynamic metabolic health status: metabolically healthy obesity (MHO), MHO to metabolically unhealthy obesity (MUO), MUO to MHO, and stable MUO. Subjects were followed up from 2009 to 2015 for incident CRC. RESULTS: The stable MHO group showed no increased risk of incident CRC (hazard ratio [HR], 0.97; 95% confidence interval [CI], 0.83–1.14). However, the MHO to MUO group had a higher risk of incident CRC than the stable metabolically healthy nonobese (MHNO) group (HR, 1.34; 95% CI, 1.15–1.57). Among patients with MUO at baseline, those in the subgroup who transitioned to MHO group were not at increased risk of CRC (HR, 1.06; 95% CI, 0.91–1.25), whereas those who remained in the stable MUO group had a higher risk of incident CRC than those in the stable MHNO group (HR, 1.29; 95% CI, 1.19–1.41). CONCLUSIONS: The transition of metabolic health was a determining factor for CRC among subjects with obesity. Hence, maintenance or recovery of metabolic health should be addressed to prevent CRC in individuals with obesity.
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spelling pubmed-78264592021-02-01 Metabolic health is a determining factor for incident colorectal cancer in the obese population: A nationwide population‐based cohort study Cho, Yun Kyung Lee, Jiwoo Kim, Hwi Seung Park, Joong‐Yeol Lee, Woo Je Kim, Ye‐Jee Jung, Chang Hee Cancer Med Clinical Cancer Research BACKGROUND: The association of the risk of colorectal cancer (CRC) with obesity or obesity‐induced metabolic disturbances remains controversial. We assessed the association of metabolic health status with incident CRC among subjects with obesity. METHODS: This study included 319,397 subjects from the Korean National Health Insurance Service‐National Health Screening Cohort. Transitions in metabolic health status and obesity were examined during 2009–2010 and 2011–2012. We categorized subjects with obesity into four separate groups according to their dynamic metabolic health status: metabolically healthy obesity (MHO), MHO to metabolically unhealthy obesity (MUO), MUO to MHO, and stable MUO. Subjects were followed up from 2009 to 2015 for incident CRC. RESULTS: The stable MHO group showed no increased risk of incident CRC (hazard ratio [HR], 0.97; 95% confidence interval [CI], 0.83–1.14). However, the MHO to MUO group had a higher risk of incident CRC than the stable metabolically healthy nonobese (MHNO) group (HR, 1.34; 95% CI, 1.15–1.57). Among patients with MUO at baseline, those in the subgroup who transitioned to MHO group were not at increased risk of CRC (HR, 1.06; 95% CI, 0.91–1.25), whereas those who remained in the stable MUO group had a higher risk of incident CRC than those in the stable MHNO group (HR, 1.29; 95% CI, 1.19–1.41). CONCLUSIONS: The transition of metabolic health was a determining factor for CRC among subjects with obesity. Hence, maintenance or recovery of metabolic health should be addressed to prevent CRC in individuals with obesity. John Wiley and Sons Inc. 2020-11-20 /pmc/articles/PMC7826459/ /pubmed/33216467 http://dx.doi.org/10.1002/cam4.3607 Text en © 2020 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Cho, Yun Kyung
Lee, Jiwoo
Kim, Hwi Seung
Park, Joong‐Yeol
Lee, Woo Je
Kim, Ye‐Jee
Jung, Chang Hee
Metabolic health is a determining factor for incident colorectal cancer in the obese population: A nationwide population‐based cohort study
title Metabolic health is a determining factor for incident colorectal cancer in the obese population: A nationwide population‐based cohort study
title_full Metabolic health is a determining factor for incident colorectal cancer in the obese population: A nationwide population‐based cohort study
title_fullStr Metabolic health is a determining factor for incident colorectal cancer in the obese population: A nationwide population‐based cohort study
title_full_unstemmed Metabolic health is a determining factor for incident colorectal cancer in the obese population: A nationwide population‐based cohort study
title_short Metabolic health is a determining factor for incident colorectal cancer in the obese population: A nationwide population‐based cohort study
title_sort metabolic health is a determining factor for incident colorectal cancer in the obese population: a nationwide population‐based cohort study
topic Clinical Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7826459/
https://www.ncbi.nlm.nih.gov/pubmed/33216467
http://dx.doi.org/10.1002/cam4.3607
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