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Calcium: magnesium intake ratio and colorectal carcinogenesis, results from the prostate, lung, colorectal, and ovarian cancer screening trial

BACKGROUND: We aimed to evaluate the associations between calcium and various stages of colorectal carcinogenesis and whether these associations are modified by the calcium to magnesium (Ca:Mg) ratio. METHODS: We tested our hypotheses in the prostate lung, colorectal and ovarian cancer screening tri...

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Autores principales: Zhao, Jing, Giri, Ayush, Zhu, Xiangzhu, Shrubsole, Martha J., Jiang, Yixing, Guo, Xingyi, Ness, Reid, Seidner, Douglas L., Giovannucci, Edward, Edwards, Todd L., Dai, Qi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889387/
https://www.ncbi.nlm.nih.gov/pubmed/31543516
http://dx.doi.org/10.1038/s41416-019-0579-2
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author Zhao, Jing
Giri, Ayush
Zhu, Xiangzhu
Shrubsole, Martha J.
Jiang, Yixing
Guo, Xingyi
Ness, Reid
Seidner, Douglas L.
Giovannucci, Edward
Edwards, Todd L.
Dai, Qi
author_facet Zhao, Jing
Giri, Ayush
Zhu, Xiangzhu
Shrubsole, Martha J.
Jiang, Yixing
Guo, Xingyi
Ness, Reid
Seidner, Douglas L.
Giovannucci, Edward
Edwards, Todd L.
Dai, Qi
author_sort Zhao, Jing
collection PubMed
description BACKGROUND: We aimed to evaluate the associations between calcium and various stages of colorectal carcinogenesis and whether these associations are modified by the calcium to magnesium (Ca:Mg) ratio. METHODS: We tested our hypotheses in the prostate lung, colorectal and ovarian cancer screening trial. RESULTS: Calcium intake did not show a dose–response association with incident adenoma of any size/stage (P-(trend) = 0.17), but followed an inverse trend when restricted to synchronous/advanced adenoma cases (P-(trend) = 0.05). This inverse trend was mainly in participants with Ca:Mg ratios between 1.7 and 2.5 (P-(trend) = 0.05). No significant associations were observed for metachronous adenoma. Calcium intake was inversely associated with CRC (P-(trend) = 0.03); the association was primarily present for distal CRC (P-(trend) = 0.01). The inverse association between calcium and distal CRC was further modified by the Ca:Mg ratio (P-(interaction) < 0.01); significant dose–response associations were found only in participants with a Ca:Mg ratio between 1.7 and 2.5 (P-(trend) = 0.04). No associations for calcium were found in the Ca:Mg ratio above 2.5 or below 1.7. CONCLUSION: Higher calcium intake may be related to reduced risks of incident advanced and/or synchronous adenoma and incident distal CRC among subjects with Ca:Mg intake ratios between 1.7 and 2.5.
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spelling pubmed-68893872020-09-23 Calcium: magnesium intake ratio and colorectal carcinogenesis, results from the prostate, lung, colorectal, and ovarian cancer screening trial Zhao, Jing Giri, Ayush Zhu, Xiangzhu Shrubsole, Martha J. Jiang, Yixing Guo, Xingyi Ness, Reid Seidner, Douglas L. Giovannucci, Edward Edwards, Todd L. Dai, Qi Br J Cancer Article BACKGROUND: We aimed to evaluate the associations between calcium and various stages of colorectal carcinogenesis and whether these associations are modified by the calcium to magnesium (Ca:Mg) ratio. METHODS: We tested our hypotheses in the prostate lung, colorectal and ovarian cancer screening trial. RESULTS: Calcium intake did not show a dose–response association with incident adenoma of any size/stage (P-(trend) = 0.17), but followed an inverse trend when restricted to synchronous/advanced adenoma cases (P-(trend) = 0.05). This inverse trend was mainly in participants with Ca:Mg ratios between 1.7 and 2.5 (P-(trend) = 0.05). No significant associations were observed for metachronous adenoma. Calcium intake was inversely associated with CRC (P-(trend) = 0.03); the association was primarily present for distal CRC (P-(trend) = 0.01). The inverse association between calcium and distal CRC was further modified by the Ca:Mg ratio (P-(interaction) < 0.01); significant dose–response associations were found only in participants with a Ca:Mg ratio between 1.7 and 2.5 (P-(trend) = 0.04). No associations for calcium were found in the Ca:Mg ratio above 2.5 or below 1.7. CONCLUSION: Higher calcium intake may be related to reduced risks of incident advanced and/or synchronous adenoma and incident distal CRC among subjects with Ca:Mg intake ratios between 1.7 and 2.5. Nature Publishing Group UK 2019-09-23 2019-10-29 /pmc/articles/PMC6889387/ /pubmed/31543516 http://dx.doi.org/10.1038/s41416-019-0579-2 Text en © The Author(s), under exclusive licence to Cancer Research UK 2019 https://creativecommons.org/licenses/by/4.0/Note: This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution 4.0 International (CC BY 4.0).
spellingShingle Article
Zhao, Jing
Giri, Ayush
Zhu, Xiangzhu
Shrubsole, Martha J.
Jiang, Yixing
Guo, Xingyi
Ness, Reid
Seidner, Douglas L.
Giovannucci, Edward
Edwards, Todd L.
Dai, Qi
Calcium: magnesium intake ratio and colorectal carcinogenesis, results from the prostate, lung, colorectal, and ovarian cancer screening trial
title Calcium: magnesium intake ratio and colorectal carcinogenesis, results from the prostate, lung, colorectal, and ovarian cancer screening trial
title_full Calcium: magnesium intake ratio and colorectal carcinogenesis, results from the prostate, lung, colorectal, and ovarian cancer screening trial
title_fullStr Calcium: magnesium intake ratio and colorectal carcinogenesis, results from the prostate, lung, colorectal, and ovarian cancer screening trial
title_full_unstemmed Calcium: magnesium intake ratio and colorectal carcinogenesis, results from the prostate, lung, colorectal, and ovarian cancer screening trial
title_short Calcium: magnesium intake ratio and colorectal carcinogenesis, results from the prostate, lung, colorectal, and ovarian cancer screening trial
title_sort calcium: magnesium intake ratio and colorectal carcinogenesis, results from the prostate, lung, colorectal, and ovarian cancer screening trial
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6889387/
https://www.ncbi.nlm.nih.gov/pubmed/31543516
http://dx.doi.org/10.1038/s41416-019-0579-2
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