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Dietary mineral intake and lung cancer risk: the Rotterdam Study

OBJECTIVE: Limited data are available on the role of mineral intake in the development of lung cancer (LC). We investigated whether dietary calcium, copper, iron, magnesium, selenium and zinc intake were associated with LC risk. METHODS: We analyzed data from 5435 participants of the Rotterdam Study...

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Autores principales: Muka, Taulant, Kraja, Bledar, Ruiter, Rikje, Lahousse, Lies, de Keyser, Catherine E., Hofman, Albert, Franco, Oscar H., Brusselle, Guy, Stricker, Bruno H., Kiefte-de Jong, Jessica C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486639/
https://www.ncbi.nlm.nih.gov/pubmed/27073037
http://dx.doi.org/10.1007/s00394-016-1210-4
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author Muka, Taulant
Kraja, Bledar
Ruiter, Rikje
Lahousse, Lies
de Keyser, Catherine E.
Hofman, Albert
Franco, Oscar H.
Brusselle, Guy
Stricker, Bruno H.
Kiefte-de Jong, Jessica C.
author_facet Muka, Taulant
Kraja, Bledar
Ruiter, Rikje
Lahousse, Lies
de Keyser, Catherine E.
Hofman, Albert
Franco, Oscar H.
Brusselle, Guy
Stricker, Bruno H.
Kiefte-de Jong, Jessica C.
author_sort Muka, Taulant
collection PubMed
description OBJECTIVE: Limited data are available on the role of mineral intake in the development of lung cancer (LC). We investigated whether dietary calcium, copper, iron, magnesium, selenium and zinc intake were associated with LC risk. METHODS: We analyzed data from 5435 participants of the Rotterdam Study, a prospective population-based cohort study among subjects aged 55 years and older. At baseline (1990–1993), diet was measured by a validated food frequency questionnaire. LC events were diagnosed on the basis of pathology data and medical records. Hazard ratios (HRs) on LC for energy-adjusted mineral intake were calculated using Cox regression models while adjusting for potential confounders. RESULTS: During a follow-up period of 22 years, we identified 211 incident cases of LC. A higher zinc intake was associated with 42 % reduction in risk of LC (top tertile vs. first tertile: HR 0.58, 95 % CI 0.35; 0.94, P-for trend = 0.039). Similarly, high intake of iron was associated with reduced risk of LC (top tertile vs. first tertile: HR 0.58, 95 % CI 0.37; 0.92, P-for trend = 0.021). There was no association between dietary intake of calcium, copper, magnesium and selenium and LC risk. CONCLUSIONS: Our results suggest that dietary zinc and iron intake are associated with reduced risk of LC. No evidence was found for an association between calcium, copper, magnesium and selenium intake and LC risk. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00394-016-1210-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-54866392017-07-11 Dietary mineral intake and lung cancer risk: the Rotterdam Study Muka, Taulant Kraja, Bledar Ruiter, Rikje Lahousse, Lies de Keyser, Catherine E. Hofman, Albert Franco, Oscar H. Brusselle, Guy Stricker, Bruno H. Kiefte-de Jong, Jessica C. Eur J Nutr Original Contribution OBJECTIVE: Limited data are available on the role of mineral intake in the development of lung cancer (LC). We investigated whether dietary calcium, copper, iron, magnesium, selenium and zinc intake were associated with LC risk. METHODS: We analyzed data from 5435 participants of the Rotterdam Study, a prospective population-based cohort study among subjects aged 55 years and older. At baseline (1990–1993), diet was measured by a validated food frequency questionnaire. LC events were diagnosed on the basis of pathology data and medical records. Hazard ratios (HRs) on LC for energy-adjusted mineral intake were calculated using Cox regression models while adjusting for potential confounders. RESULTS: During a follow-up period of 22 years, we identified 211 incident cases of LC. A higher zinc intake was associated with 42 % reduction in risk of LC (top tertile vs. first tertile: HR 0.58, 95 % CI 0.35; 0.94, P-for trend = 0.039). Similarly, high intake of iron was associated with reduced risk of LC (top tertile vs. first tertile: HR 0.58, 95 % CI 0.37; 0.92, P-for trend = 0.021). There was no association between dietary intake of calcium, copper, magnesium and selenium and LC risk. CONCLUSIONS: Our results suggest that dietary zinc and iron intake are associated with reduced risk of LC. No evidence was found for an association between calcium, copper, magnesium and selenium intake and LC risk. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00394-016-1210-4) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-04-12 2017 /pmc/articles/PMC5486639/ /pubmed/27073037 http://dx.doi.org/10.1007/s00394-016-1210-4 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Contribution
Muka, Taulant
Kraja, Bledar
Ruiter, Rikje
Lahousse, Lies
de Keyser, Catherine E.
Hofman, Albert
Franco, Oscar H.
Brusselle, Guy
Stricker, Bruno H.
Kiefte-de Jong, Jessica C.
Dietary mineral intake and lung cancer risk: the Rotterdam Study
title Dietary mineral intake and lung cancer risk: the Rotterdam Study
title_full Dietary mineral intake and lung cancer risk: the Rotterdam Study
title_fullStr Dietary mineral intake and lung cancer risk: the Rotterdam Study
title_full_unstemmed Dietary mineral intake and lung cancer risk: the Rotterdam Study
title_short Dietary mineral intake and lung cancer risk: the Rotterdam Study
title_sort dietary mineral intake and lung cancer risk: the rotterdam study
topic Original Contribution
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5486639/
https://www.ncbi.nlm.nih.gov/pubmed/27073037
http://dx.doi.org/10.1007/s00394-016-1210-4
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