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Association of visceral adiposity and insulin resistance with colorectal adenoma and colorectal cancer

BACKGROUND/AIMS: To examine whether visceral adiposity serves as a risk factor for colorectal cancer (CRC) and colorectal adenomas. METHODS: Two hundred healthy subjects, 200 patients with colorectal adenoma, and 151 patients with CRC (46 with early-stage and 105 with advanced-stage cancers) were en...

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Autores principales: Jung, In Sub, Shin, Cheol Min, Park, Sung Jae, Park, Young Soo, Yoon, Hyuk, Jo, Hyun Jin, Kim, Nayoung, Lee, Dong Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association for the Study of Intestinal Diseases 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6667358/
https://www.ncbi.nlm.nih.gov/pubmed/30419640
http://dx.doi.org/10.5217/ir.2018.00072
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author Jung, In Sub
Shin, Cheol Min
Park, Sung Jae
Park, Young Soo
Yoon, Hyuk
Jo, Hyun Jin
Kim, Nayoung
Lee, Dong Ho
author_facet Jung, In Sub
Shin, Cheol Min
Park, Sung Jae
Park, Young Soo
Yoon, Hyuk
Jo, Hyun Jin
Kim, Nayoung
Lee, Dong Ho
author_sort Jung, In Sub
collection PubMed
description BACKGROUND/AIMS: To examine whether visceral adiposity serves as a risk factor for colorectal cancer (CRC) and colorectal adenomas. METHODS: Two hundred healthy subjects, 200 patients with colorectal adenoma, and 151 patients with CRC (46 with early-stage and 105 with advanced-stage cancers) were enrolled at a tertiary referral hospital. All subjects underwent colonoscopy, and had laboratory data, and computed tomography (CT) scan available for abdominal fat measurement. An abdominal CT scan taken 1 to 4 years (mean interval, 20.6 months) before the diagnosis of CRC was also available in the 42 CRC patients. RESULTS: The mean areas of visceral adipose tissue (VAT) areas in the control, adenoma, early- and advanced-stage CRC groups were 94.6, 116.8, 110.4, and 99.7 cm(2), respectively (P<0.001). The risk of adenoma positively correlated with VAT area and the visceral-to-total fat ratio (P for trend <0.01), but the risk of CRC did not (P>0.05). The risk of both adenoma and CRC positively correlated with fasting plasma glucose levels (P for trend <0.05). In patients with early-stage cancer (n=17), VAT area decreased when the CT scan at diagnosis was compared with that taken before the diagnosis of CRC, but superficial adipose tissue area did not, so visceral-to-total fat ratio significantly decreased (46.6% vs. 50.7%, respectively, P=0.018) CONCLUSIONS: VAT area is related to the risk of colorectal adenoma. However, VAT decreases from the early stages of CRC. Impaired fasting glucose has a role in colorectal carcinogenesis.
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spelling pubmed-66673582019-07-31 Association of visceral adiposity and insulin resistance with colorectal adenoma and colorectal cancer Jung, In Sub Shin, Cheol Min Park, Sung Jae Park, Young Soo Yoon, Hyuk Jo, Hyun Jin Kim, Nayoung Lee, Dong Ho Intest Res Original Article BACKGROUND/AIMS: To examine whether visceral adiposity serves as a risk factor for colorectal cancer (CRC) and colorectal adenomas. METHODS: Two hundred healthy subjects, 200 patients with colorectal adenoma, and 151 patients with CRC (46 with early-stage and 105 with advanced-stage cancers) were enrolled at a tertiary referral hospital. All subjects underwent colonoscopy, and had laboratory data, and computed tomography (CT) scan available for abdominal fat measurement. An abdominal CT scan taken 1 to 4 years (mean interval, 20.6 months) before the diagnosis of CRC was also available in the 42 CRC patients. RESULTS: The mean areas of visceral adipose tissue (VAT) areas in the control, adenoma, early- and advanced-stage CRC groups were 94.6, 116.8, 110.4, and 99.7 cm(2), respectively (P<0.001). The risk of adenoma positively correlated with VAT area and the visceral-to-total fat ratio (P for trend <0.01), but the risk of CRC did not (P>0.05). The risk of both adenoma and CRC positively correlated with fasting plasma glucose levels (P for trend <0.05). In patients with early-stage cancer (n=17), VAT area decreased when the CT scan at diagnosis was compared with that taken before the diagnosis of CRC, but superficial adipose tissue area did not, so visceral-to-total fat ratio significantly decreased (46.6% vs. 50.7%, respectively, P=0.018) CONCLUSIONS: VAT area is related to the risk of colorectal adenoma. However, VAT decreases from the early stages of CRC. Impaired fasting glucose has a role in colorectal carcinogenesis. Korean Association for the Study of Intestinal Diseases 2019-07 2018-11-12 /pmc/articles/PMC6667358/ /pubmed/30419640 http://dx.doi.org/10.5217/ir.2018.00072 Text en © Copyright 2019. Korean Association for the Study of Intestinal Diseases. All rights reserved. This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Jung, In Sub
Shin, Cheol Min
Park, Sung Jae
Park, Young Soo
Yoon, Hyuk
Jo, Hyun Jin
Kim, Nayoung
Lee, Dong Ho
Association of visceral adiposity and insulin resistance with colorectal adenoma and colorectal cancer
title Association of visceral adiposity and insulin resistance with colorectal adenoma and colorectal cancer
title_full Association of visceral adiposity and insulin resistance with colorectal adenoma and colorectal cancer
title_fullStr Association of visceral adiposity and insulin resistance with colorectal adenoma and colorectal cancer
title_full_unstemmed Association of visceral adiposity and insulin resistance with colorectal adenoma and colorectal cancer
title_short Association of visceral adiposity and insulin resistance with colorectal adenoma and colorectal cancer
title_sort association of visceral adiposity and insulin resistance with colorectal adenoma and colorectal cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6667358/
https://www.ncbi.nlm.nih.gov/pubmed/30419640
http://dx.doi.org/10.5217/ir.2018.00072
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