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Dietary advanced glycation end products and cancer risk in Japan: From the Takayama study

Few large epidemiological studies have evaluated the association between dietary advanced glycation end products (AGEs) and cancer risk. We evaluated the relationship between dietary AGE intake and the incidence of total cancer and site‐specific cancers in a population‐based prospective study in Jap...

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Autores principales: Wada, Keiko, Nakashima, Yuma, Yamakawa, Michiyo, Hori, Akihiro, Seishima, Mitsuru, Tanabashi, Shinobu, Matsushita, Shogen, Tokimitsu, Naoki, Nagata, Chisato
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9357612/
https://www.ncbi.nlm.nih.gov/pubmed/35662347
http://dx.doi.org/10.1111/cas.15455
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author Wada, Keiko
Nakashima, Yuma
Yamakawa, Michiyo
Hori, Akihiro
Seishima, Mitsuru
Tanabashi, Shinobu
Matsushita, Shogen
Tokimitsu, Naoki
Nagata, Chisato
author_facet Wada, Keiko
Nakashima, Yuma
Yamakawa, Michiyo
Hori, Akihiro
Seishima, Mitsuru
Tanabashi, Shinobu
Matsushita, Shogen
Tokimitsu, Naoki
Nagata, Chisato
author_sort Wada, Keiko
collection PubMed
description Few large epidemiological studies have evaluated the association between dietary advanced glycation end products (AGEs) and cancer risk. We evaluated the relationship between dietary AGE intake and the incidence of total cancer and site‐specific cancers in a population‐based prospective study in Japan. Participants were 14,173 men and 16,549 women who were 35 years of age or older in 1992. Dietary intake was assessed via a validated food frequency questionnaire. Intake of the AGE N (ε)‐carboxymethyl‐lysine (CML) was estimated using databases of CML content in foods determined using ultraperformance liquid chromatography–tandem mass spectrometry. Cancer incidence was confirmed through regional population‐based cancer registries. During a mean follow‐up period of 13.3 years, 1954 men and 1477 women developed cancer. We did not observe a significant association between CML intake and the risk of total cancer in men or women. In men, compared with the lowest quartile of CML intake, the hazard ratios of liver cancer for the second, third, and highest quartiles were 1.69 (95% CI: 0.92–3.10), 1.48 (95% CI: 0.77–2.84), and 2.10 (95% CI: 1.10–3.98; trend p = 0.04). Conversely, a decreased relative risk of male stomach cancer was observed for the second and highest quartiles of CML intake versus the lowest quartile, with hazard ratios of 0.73 and 0.67, respectively (trend p = 0.08). Our finding on the potential harmfulness of consuming AGEs on liver cancer risk is intriguing and warrants further study.
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spelling pubmed-93576122022-08-09 Dietary advanced glycation end products and cancer risk in Japan: From the Takayama study Wada, Keiko Nakashima, Yuma Yamakawa, Michiyo Hori, Akihiro Seishima, Mitsuru Tanabashi, Shinobu Matsushita, Shogen Tokimitsu, Naoki Nagata, Chisato Cancer Sci ORIGINAL ARTICLES Few large epidemiological studies have evaluated the association between dietary advanced glycation end products (AGEs) and cancer risk. We evaluated the relationship between dietary AGE intake and the incidence of total cancer and site‐specific cancers in a population‐based prospective study in Japan. Participants were 14,173 men and 16,549 women who were 35 years of age or older in 1992. Dietary intake was assessed via a validated food frequency questionnaire. Intake of the AGE N (ε)‐carboxymethyl‐lysine (CML) was estimated using databases of CML content in foods determined using ultraperformance liquid chromatography–tandem mass spectrometry. Cancer incidence was confirmed through regional population‐based cancer registries. During a mean follow‐up period of 13.3 years, 1954 men and 1477 women developed cancer. We did not observe a significant association between CML intake and the risk of total cancer in men or women. In men, compared with the lowest quartile of CML intake, the hazard ratios of liver cancer for the second, third, and highest quartiles were 1.69 (95% CI: 0.92–3.10), 1.48 (95% CI: 0.77–2.84), and 2.10 (95% CI: 1.10–3.98; trend p = 0.04). Conversely, a decreased relative risk of male stomach cancer was observed for the second and highest quartiles of CML intake versus the lowest quartile, with hazard ratios of 0.73 and 0.67, respectively (trend p = 0.08). Our finding on the potential harmfulness of consuming AGEs on liver cancer risk is intriguing and warrants further study. John Wiley and Sons Inc. 2022-06-25 2022-08 /pmc/articles/PMC9357612/ /pubmed/35662347 http://dx.doi.org/10.1111/cas.15455 Text en © 2022 The Authors. Cancer Science published by John Wiley & Sons Australia, Ltd on behalf of Japanese Cancer Association. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle ORIGINAL ARTICLES
Wada, Keiko
Nakashima, Yuma
Yamakawa, Michiyo
Hori, Akihiro
Seishima, Mitsuru
Tanabashi, Shinobu
Matsushita, Shogen
Tokimitsu, Naoki
Nagata, Chisato
Dietary advanced glycation end products and cancer risk in Japan: From the Takayama study
title Dietary advanced glycation end products and cancer risk in Japan: From the Takayama study
title_full Dietary advanced glycation end products and cancer risk in Japan: From the Takayama study
title_fullStr Dietary advanced glycation end products and cancer risk in Japan: From the Takayama study
title_full_unstemmed Dietary advanced glycation end products and cancer risk in Japan: From the Takayama study
title_short Dietary advanced glycation end products and cancer risk in Japan: From the Takayama study
title_sort dietary advanced glycation end products and cancer risk in japan: from the takayama study
topic ORIGINAL ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9357612/
https://www.ncbi.nlm.nih.gov/pubmed/35662347
http://dx.doi.org/10.1111/cas.15455
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