Low folate levels may protect against colorectal cancer

Background and aims: Dietary folate is believed to protect against colorectal cancer (CRC). However, few studies have addressed the role of circulating levels of folate. The aim of this study was to relate prediagnostic plasma folate and homocysteine concentrations and the methylenetetrahydrofolate...

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Published in:Gut
Main Authors: Van Guelpen, B, Hultdin, J, Johansson, I, Hallmans, G, Stenling, R, Riboli, E, Winkvist, A, Palmqvist, R
Format: Text
Language:English
Published: BMJ Publishing Group Ltd 2006
Subjects:
Online Access:http://gut.bmj.com/cgi/content/short/55/10/1461
https://doi.org/10.1136/gut.2005.085480
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spelling fthighwire:oai:open-archive.highwire.org:gutjnl:55/10/1461 2023-05-15T17:44:53+02:00 Low folate levels may protect against colorectal cancer Van Guelpen, B Hultdin, J Johansson, I Hallmans, G Stenling, R Riboli, E Winkvist, A Palmqvist, R 2006-10-01 00:00:00.0 text/html http://gut.bmj.com/cgi/content/short/55/10/1461 https://doi.org/10.1136/gut.2005.085480 en eng BMJ Publishing Group Ltd http://gut.bmj.com/cgi/content/short/55/10/1461 http://dx.doi.org/10.1136/gut.2005.085480 Copyright (C) 2006, BMJ Publishing Group Colorectal cancer TEXT 2006 fthighwire https://doi.org/10.1136/gut.2005.085480 2013-05-27T11:20:05Z Background and aims: Dietary folate is believed to protect against colorectal cancer (CRC). However, few studies have addressed the role of circulating levels of folate. The aim of this study was to relate prediagnostic plasma folate and homocysteine concentrations and the methylenetetrahydrofolate reductase (MTHFR) 677C>T and 1298A>C polymorphisms to the risk of developing CRC. Subjects: Subjects were 226 cases and 437 matched referents from the population based Northern Sweden Health and Disease Cohort. Results: We observed a bell-shaped association between plasma folate concentrations and CRC risk; multivariate odds ratio for middle versus lowest quintile 2.00 (95% confidence interval (CI) 1.13–3.56). In subjects with follow up times greater than the median of 4.2 years however, plasma folate concentrations were strongly positively related to CRC risk; multivariate odds ratio for highest versus lowest quintile 3.87 (95% CI 1.52–9.87; p trend = 0.007). Homocysteine was not associated with CRC risk. Multivariate odds ratios for the MTHFR polymorphisms were, for 677 TT versus CC, 0.41 (95% CI 0.19–0.85; p trend = 0.062), and for 1298 CC versus AA, 1.62 (95% CI 0.94–2.81; p trend = 0.028). Interaction analysis suggested that the result for 1298A>C may have been largely due to linkage disequilibrium with 677C>T. The reduced CRC risk in 677 TT homozygotes was independent of plasma folate status. Conclusions: Our findings suggest a decreased CRC risk in subjects with low folate status. This possibility of a detrimental component to the role of folate in carcinogenesis could have implications in the ongoing debate in Europe concerning mandatory folate fortification of foods. Text Northern Sweden HighWire Press (Stanford University) Gut 55 10 1461 1466
institution Open Polar
collection HighWire Press (Stanford University)
op_collection_id fthighwire
language English
topic Colorectal cancer
spellingShingle Colorectal cancer
Van Guelpen, B
Hultdin, J
Johansson, I
Hallmans, G
Stenling, R
Riboli, E
Winkvist, A
Palmqvist, R
Low folate levels may protect against colorectal cancer
topic_facet Colorectal cancer
description Background and aims: Dietary folate is believed to protect against colorectal cancer (CRC). However, few studies have addressed the role of circulating levels of folate. The aim of this study was to relate prediagnostic plasma folate and homocysteine concentrations and the methylenetetrahydrofolate reductase (MTHFR) 677C>T and 1298A>C polymorphisms to the risk of developing CRC. Subjects: Subjects were 226 cases and 437 matched referents from the population based Northern Sweden Health and Disease Cohort. Results: We observed a bell-shaped association between plasma folate concentrations and CRC risk; multivariate odds ratio for middle versus lowest quintile 2.00 (95% confidence interval (CI) 1.13–3.56). In subjects with follow up times greater than the median of 4.2 years however, plasma folate concentrations were strongly positively related to CRC risk; multivariate odds ratio for highest versus lowest quintile 3.87 (95% CI 1.52–9.87; p trend = 0.007). Homocysteine was not associated with CRC risk. Multivariate odds ratios for the MTHFR polymorphisms were, for 677 TT versus CC, 0.41 (95% CI 0.19–0.85; p trend = 0.062), and for 1298 CC versus AA, 1.62 (95% CI 0.94–2.81; p trend = 0.028). Interaction analysis suggested that the result for 1298A>C may have been largely due to linkage disequilibrium with 677C>T. The reduced CRC risk in 677 TT homozygotes was independent of plasma folate status. Conclusions: Our findings suggest a decreased CRC risk in subjects with low folate status. This possibility of a detrimental component to the role of folate in carcinogenesis could have implications in the ongoing debate in Europe concerning mandatory folate fortification of foods.
format Text
author Van Guelpen, B
Hultdin, J
Johansson, I
Hallmans, G
Stenling, R
Riboli, E
Winkvist, A
Palmqvist, R
author_facet Van Guelpen, B
Hultdin, J
Johansson, I
Hallmans, G
Stenling, R
Riboli, E
Winkvist, A
Palmqvist, R
author_sort Van Guelpen, B
title Low folate levels may protect against colorectal cancer
title_short Low folate levels may protect against colorectal cancer
title_full Low folate levels may protect against colorectal cancer
title_fullStr Low folate levels may protect against colorectal cancer
title_full_unstemmed Low folate levels may protect against colorectal cancer
title_sort low folate levels may protect against colorectal cancer
publisher BMJ Publishing Group Ltd
publishDate 2006
url http://gut.bmj.com/cgi/content/short/55/10/1461
https://doi.org/10.1136/gut.2005.085480
genre Northern Sweden
genre_facet Northern Sweden
op_relation http://gut.bmj.com/cgi/content/short/55/10/1461
http://dx.doi.org/10.1136/gut.2005.085480
op_rights Copyright (C) 2006, BMJ Publishing Group
op_doi https://doi.org/10.1136/gut.2005.085480
container_title Gut
container_volume 55
container_issue 10
container_start_page 1461
op_container_end_page 1466
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