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Dietary iron intake and breast cancer risk: modulation by an antioxidant supplementation

Experimental results suggested that iron-induced lipid peroxidation may explain the direct associations observed between red/processed meat intakes and colorectal and breast cancer risk. However, epidemiological evidence is lacking. Thus, we investigated the association between dietary iron intake a...

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Autores principales: Diallo, Abou, Deschasaux, Mélanie, Partula, Valentin, Latino-Martel, Paule, Srour, Bernard, Hercberg, Serge, Galan, Pilar, Fassier, Philippine, Guéraud, Françoise, Pierre, Fabrice H., Touvier, Mathilde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346694/
https://www.ncbi.nlm.nih.gov/pubmed/27738321
http://dx.doi.org/10.18632/oncotarget.12592
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author Diallo, Abou
Deschasaux, Mélanie
Partula, Valentin
Latino-Martel, Paule
Srour, Bernard
Hercberg, Serge
Galan, Pilar
Fassier, Philippine
Guéraud, Françoise
Pierre, Fabrice H.
Touvier, Mathilde
author_facet Diallo, Abou
Deschasaux, Mélanie
Partula, Valentin
Latino-Martel, Paule
Srour, Bernard
Hercberg, Serge
Galan, Pilar
Fassier, Philippine
Guéraud, Françoise
Pierre, Fabrice H.
Touvier, Mathilde
author_sort Diallo, Abou
collection PubMed
description Experimental results suggested that iron-induced lipid peroxidation may explain the direct associations observed between red/processed meat intakes and colorectal and breast cancer risk. However, epidemiological evidence is lacking. Thus, we investigated the association between dietary iron intake and breast cancer risk, and its potential modulation by an antioxidant supplementation and lipid intake. This prospective study included 4646 women from the SU.VI.MAX trial (daily low-dose antioxidants vs. placebo). 188 incident breast cancers were diagnosed (median follow-up=12.6y). Dietary iron intake was assessed using repeated 24h dietary records. Multivariable Cox proportional hazards models were computed. Dietary iron intake was associated with an increased breast cancer risk (HR(T3vs.T1)=1.67 (1.02-2.71), P-trend=0.04). This association was observed in the placebo group (HR(T3vs.T1)=2.80 (1.42-5.54), P-trend=0.003), but not in the antioxidant-supplemented group (P-trend=0.7, P-interaction=0.1). Besides, in the placebo group, the increased breast cancer risk associated with dietary iron intake was more specifically observed in women with higher lipid intake (P-trend=0.046). These findings suggest that dietary iron intake may be associated with an increased breast cancer risk, especially in women who did not received antioxidants during the trial and who consumed more lipids. This supports the experimental results suggesting that breast cancer risk may be increased by iron-induced lipid peroxidation.
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spelling pubmed-53466942017-03-30 Dietary iron intake and breast cancer risk: modulation by an antioxidant supplementation Diallo, Abou Deschasaux, Mélanie Partula, Valentin Latino-Martel, Paule Srour, Bernard Hercberg, Serge Galan, Pilar Fassier, Philippine Guéraud, Françoise Pierre, Fabrice H. Touvier, Mathilde Oncotarget Research Paper Experimental results suggested that iron-induced lipid peroxidation may explain the direct associations observed between red/processed meat intakes and colorectal and breast cancer risk. However, epidemiological evidence is lacking. Thus, we investigated the association between dietary iron intake and breast cancer risk, and its potential modulation by an antioxidant supplementation and lipid intake. This prospective study included 4646 women from the SU.VI.MAX trial (daily low-dose antioxidants vs. placebo). 188 incident breast cancers were diagnosed (median follow-up=12.6y). Dietary iron intake was assessed using repeated 24h dietary records. Multivariable Cox proportional hazards models were computed. Dietary iron intake was associated with an increased breast cancer risk (HR(T3vs.T1)=1.67 (1.02-2.71), P-trend=0.04). This association was observed in the placebo group (HR(T3vs.T1)=2.80 (1.42-5.54), P-trend=0.003), but not in the antioxidant-supplemented group (P-trend=0.7, P-interaction=0.1). Besides, in the placebo group, the increased breast cancer risk associated with dietary iron intake was more specifically observed in women with higher lipid intake (P-trend=0.046). These findings suggest that dietary iron intake may be associated with an increased breast cancer risk, especially in women who did not received antioxidants during the trial and who consumed more lipids. This supports the experimental results suggesting that breast cancer risk may be increased by iron-induced lipid peroxidation. Impact Journals LLC 2016-10-12 /pmc/articles/PMC5346694/ /pubmed/27738321 http://dx.doi.org/10.18632/oncotarget.12592 Text en Copyright: © 2016 Diallo et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Diallo, Abou
Deschasaux, Mélanie
Partula, Valentin
Latino-Martel, Paule
Srour, Bernard
Hercberg, Serge
Galan, Pilar
Fassier, Philippine
Guéraud, Françoise
Pierre, Fabrice H.
Touvier, Mathilde
Dietary iron intake and breast cancer risk: modulation by an antioxidant supplementation
title Dietary iron intake and breast cancer risk: modulation by an antioxidant supplementation
title_full Dietary iron intake and breast cancer risk: modulation by an antioxidant supplementation
title_fullStr Dietary iron intake and breast cancer risk: modulation by an antioxidant supplementation
title_full_unstemmed Dietary iron intake and breast cancer risk: modulation by an antioxidant supplementation
title_short Dietary iron intake and breast cancer risk: modulation by an antioxidant supplementation
title_sort dietary iron intake and breast cancer risk: modulation by an antioxidant supplementation
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346694/
https://www.ncbi.nlm.nih.gov/pubmed/27738321
http://dx.doi.org/10.18632/oncotarget.12592
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