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Metabolic risk factors for esophageal squamous cell carcinoma and adenocarcinoma: a prospective study of 580 000 subjects within the Me-Can project

BACKGROUND: Obesity is associated with an increased risk of esophageal adenocarcinoma (EAC) and a decreased risk of esophageal squamous cell carcinoma (ESCC). However, little is known about the risk of EAC and ESCC related to other metabolic risk factors. We aimed to examine the risk of EAC and ESCC...

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Autores principales: Lindkvist, Björn, Johansen, Dorthe, Stocks, Tanja, Concin, Hans, Bjørge, Tone, Almquist, Martin, Häggström, Christel, Engeland, Anders, Hallmans, Göran, Nagel, Gabriele, Jonsson, Håkan, Selmer, Randi, Ulmer, Hanno, Tretli, Steinar, Stattin, Pär, Manjer, Jonas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929907/
https://www.ncbi.nlm.nih.gov/pubmed/24548688
http://dx.doi.org/10.1186/1471-2407-14-103
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author Lindkvist, Björn
Johansen, Dorthe
Stocks, Tanja
Concin, Hans
Bjørge, Tone
Almquist, Martin
Häggström, Christel
Engeland, Anders
Hallmans, Göran
Nagel, Gabriele
Jonsson, Håkan
Selmer, Randi
Ulmer, Hanno
Tretli, Steinar
Stattin, Pär
Manjer, Jonas
author_facet Lindkvist, Björn
Johansen, Dorthe
Stocks, Tanja
Concin, Hans
Bjørge, Tone
Almquist, Martin
Häggström, Christel
Engeland, Anders
Hallmans, Göran
Nagel, Gabriele
Jonsson, Håkan
Selmer, Randi
Ulmer, Hanno
Tretli, Steinar
Stattin, Pär
Manjer, Jonas
author_sort Lindkvist, Björn
collection PubMed
description BACKGROUND: Obesity is associated with an increased risk of esophageal adenocarcinoma (EAC) and a decreased risk of esophageal squamous cell carcinoma (ESCC). However, little is known about the risk of EAC and ESCC related to other metabolic risk factors. We aimed to examine the risk of EAC and ESCC in relation to metabolic risk factors, separately and combined in a prospective cohort study. METHODS: The Metabolic Syndrome and Cancer cohort includes prospective cohorts in Austria, Norway and Sweden, with blood pressure, lipids, glucose and BMI available from 578 700 individuals. Relative risk (RR) for EAC and ESCC was calculated using Cox’s proportional hazards analysis for metabolic risk factors categorized into quintiles and transformed into z-scores. The standardized sum of all z-scores was used as a composite score for the metabolic syndrome (MetS). RESULTS: In total, 324 histologically verified cases of esophageal cancer were identified (114 EAC, 184 ESCC and 26 with other histology). BMI was associated with an increased risk of EAC (RR 7.34 (95% confidence interval, 2.88-18.7) top versus bottom quintile) and negatively associated with the risk of ESCC (RR 0.38 (0.23-0.62)). The mean value of systolic and diastolic blood pressure (mid blood pressure) was associated with the risk of ESCC (RR 1.77 (1.37-2.29)). The composite MetS score was associated with the risk of EAC (RR 1.56 (1.19-2.05) per one unit increase of z-score) but not ESCC. CONCLUSIONS: In accordance with previous studies, high BMI was associated with an increased risk of EAC and a decreased risk of ESCC. An association between high blood pressure and risk of ESCC was observed but alcohol consumption is a potential confounding factor that we were not able to adjust for in the analysis. The MetS was associated with EAC but not ESCC. However this association was largely driven by the strong association between BMI and EAC. We hypothesize that this association is more likely to be explained by factors directly related to obesity than the metabolic state of the MetS, considering that no other metabolic factor than BMI was associated with EAC.
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spelling pubmed-39299072014-02-21 Metabolic risk factors for esophageal squamous cell carcinoma and adenocarcinoma: a prospective study of 580 000 subjects within the Me-Can project Lindkvist, Björn Johansen, Dorthe Stocks, Tanja Concin, Hans Bjørge, Tone Almquist, Martin Häggström, Christel Engeland, Anders Hallmans, Göran Nagel, Gabriele Jonsson, Håkan Selmer, Randi Ulmer, Hanno Tretli, Steinar Stattin, Pär Manjer, Jonas BMC Cancer Research Article BACKGROUND: Obesity is associated with an increased risk of esophageal adenocarcinoma (EAC) and a decreased risk of esophageal squamous cell carcinoma (ESCC). However, little is known about the risk of EAC and ESCC related to other metabolic risk factors. We aimed to examine the risk of EAC and ESCC in relation to metabolic risk factors, separately and combined in a prospective cohort study. METHODS: The Metabolic Syndrome and Cancer cohort includes prospective cohorts in Austria, Norway and Sweden, with blood pressure, lipids, glucose and BMI available from 578 700 individuals. Relative risk (RR) for EAC and ESCC was calculated using Cox’s proportional hazards analysis for metabolic risk factors categorized into quintiles and transformed into z-scores. The standardized sum of all z-scores was used as a composite score for the metabolic syndrome (MetS). RESULTS: In total, 324 histologically verified cases of esophageal cancer were identified (114 EAC, 184 ESCC and 26 with other histology). BMI was associated with an increased risk of EAC (RR 7.34 (95% confidence interval, 2.88-18.7) top versus bottom quintile) and negatively associated with the risk of ESCC (RR 0.38 (0.23-0.62)). The mean value of systolic and diastolic blood pressure (mid blood pressure) was associated with the risk of ESCC (RR 1.77 (1.37-2.29)). The composite MetS score was associated with the risk of EAC (RR 1.56 (1.19-2.05) per one unit increase of z-score) but not ESCC. CONCLUSIONS: In accordance with previous studies, high BMI was associated with an increased risk of EAC and a decreased risk of ESCC. An association between high blood pressure and risk of ESCC was observed but alcohol consumption is a potential confounding factor that we were not able to adjust for in the analysis. The MetS was associated with EAC but not ESCC. However this association was largely driven by the strong association between BMI and EAC. We hypothesize that this association is more likely to be explained by factors directly related to obesity than the metabolic state of the MetS, considering that no other metabolic factor than BMI was associated with EAC. BioMed Central 2014-02-18 /pmc/articles/PMC3929907/ /pubmed/24548688 http://dx.doi.org/10.1186/1471-2407-14-103 Text en Copyright © 2014 Lindkvist et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited.
spellingShingle Research Article
Lindkvist, Björn
Johansen, Dorthe
Stocks, Tanja
Concin, Hans
Bjørge, Tone
Almquist, Martin
Häggström, Christel
Engeland, Anders
Hallmans, Göran
Nagel, Gabriele
Jonsson, Håkan
Selmer, Randi
Ulmer, Hanno
Tretli, Steinar
Stattin, Pär
Manjer, Jonas
Metabolic risk factors for esophageal squamous cell carcinoma and adenocarcinoma: a prospective study of 580 000 subjects within the Me-Can project
title Metabolic risk factors for esophageal squamous cell carcinoma and adenocarcinoma: a prospective study of 580 000 subjects within the Me-Can project
title_full Metabolic risk factors for esophageal squamous cell carcinoma and adenocarcinoma: a prospective study of 580 000 subjects within the Me-Can project
title_fullStr Metabolic risk factors for esophageal squamous cell carcinoma and adenocarcinoma: a prospective study of 580 000 subjects within the Me-Can project
title_full_unstemmed Metabolic risk factors for esophageal squamous cell carcinoma and adenocarcinoma: a prospective study of 580 000 subjects within the Me-Can project
title_short Metabolic risk factors for esophageal squamous cell carcinoma and adenocarcinoma: a prospective study of 580 000 subjects within the Me-Can project
title_sort metabolic risk factors for esophageal squamous cell carcinoma and adenocarcinoma: a prospective study of 580 000 subjects within the me-can project
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929907/
https://www.ncbi.nlm.nih.gov/pubmed/24548688
http://dx.doi.org/10.1186/1471-2407-14-103
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