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@ARTICLE{Aglago:172519,
author = {E. K. Aglago and A.-L. Mayén and V. Knaze and H. Freisling
and V. Fedirko and D. J. Hughes and L. Jiao and A. K.
Eriksen and A. Tjønneland and M.-C. Boutron-Ruault and J.
A. Rothwell and G. Severi and R. Kaaks$^*$ and V. Katzke$^*$
and M. B. Schulze and A. Birukov and D. Palli and S. Sieri
and M. Santucci de Magistris and R. Tumino and F. Ricceri
and B. Bueno-de-Mesquita and J. W. G. Derksen and G. Skeie
and I. T. Gram and T. Sandanger and J. R. Quirós and L.
Luján-Barroso and M.-J. Sánchez and P. Amiano and M.-D.
Chirlaque and A. B. Gurrea and I. Johansson and J. Manjer
and A. Perez-Cornago and E. Weiderpass and M. J. Gunter and
A. K. Heath and C. G. Schalkwijk and M. Jenab},
title = {{D}ietary {A}dvanced {G}lycation {E}nd-{P}roducts and
{C}olorectal {C}ancer {R}isk in the {E}uropean {P}rospective
{I}nvestigation into {C}ancer and {N}utrition ({EPIC})
{S}tudy.},
journal = {Nutrients},
volume = {13},
number = {9},
issn = {2072-6643},
address = {Basel},
publisher = {MDPI},
reportid = {DKFZ-2021-02067},
pages = {3132},
year = {2021},
abstract = {Dietary advanced glycation end-products (dAGEs) have been
hypothesized to be associated with a higher risk of
colorectal cancer (CRC) by promoting inflammation, metabolic
dysfunction, and oxidative stress in the colonic epithelium.
However, evidence from prospective cohort studies is scarce
and inconclusive. We evaluated CRC risk associated with the
intake of dAGEs in the European Prospective Investigation
into Cancer and Nutrition (EPIC) study. Dietary intakes of
three major dAGEs: Nε-carboxy-methyllysine (CML),
Nε-carboxyethyllysine (CEL), and
Nδ-(5-hydro-5-methyl-4-imidazolon-2-yl)-ornithine (MG-H1)
were estimated in 450,111 participants (median follow-up =
13 years, with 6162 CRC cases) by matching to a detailed
published European food composition database. Hazard ratios
(HRs) and $95\%$ confidence intervals (CIs) for the
associations of dAGEs with CRC were computed using
multivariable-adjusted Cox regression models. Inverse CRC
risk associations were observed for CML (HR comparing
extreme quintiles: HRQ5vs.Q1 = 0.92, $95\%$ CI = 0.85-1.00)
and MG-H1 (HRQ5vs.Q1 = 0.92, $95\%$ CI = 0.85-1.00), but not
for CEL (HRQ5vs.Q1 = 0.97, $95\%$ CI = 0.89-1.05). The
associations did not differ by sex or anatomical location of
the tumor. Contrary to the initial hypothesis, our findings
suggest an inverse association between dAGEs and CRC risk.
More research is required to verify these findings and
better differentiate the role of dAGEs from that of
endogenously produced AGEs and their precursor compounds in
CRC development.},
keywords = {advanced glycation end-products (Other) / colorectal cancer
(Other) / dietary exposure (Other) / dietary glycation
compounds (Other)},
cin = {C020},
ddc = {610},
cid = {I:(DE-He78)C020-20160331},
pnm = {313 - Krebsrisikofaktoren und Prävention (POF4-313)},
pid = {G:(DE-HGF)POF4-313},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:34579010},
pmc = {pmc:PMC8470201},
doi = {10.3390/nu13093132},
url = {https://inrepo02.dkfz.de/record/172519},
}