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@ARTICLE{Archambault:168982,
author = {A. N. Archambault and Y. Lin and J. Jeon and T. A. Harrison
and D. T. Bishop and H. Brenner$^*$ and G. Casey and A. T.
Chan and J. Chang-Claude$^*$ and J. C. Figueiredo and S.
Gallinger and S. B. Gruber and M. J. Gunter and M.
Hoffmeister$^*$ and M. A. Jenkins and T. O. Keku and L. L.
Marchand and L. Li and V. Moreno and P. A. Newcomb and R.
Pai and P. S. Parfrey and G. Rennert and L. C. Sakoda and R.
S. Sandler and M. L. Slattery and M. Song and A. K. Win and
M. O. Woods and N. Murphy and P. T. Campbell and Y.-R. Su
and A. Zeleniuch-Jacquotte and P. S. Liang and M. Du and L.
Hsu and U. Peters and R. B. Hayes},
title = {{N}ongenetic {D}eterminants of {R}isk for {E}arly-{O}nset
{C}olorectal {C}ancer.},
journal = {JNCI cancer spectrum},
volume = {5},
number = {3},
issn = {2515-5091},
address = {Oxford},
publisher = {Oxford University Press},
reportid = {DKFZ-2021-01178},
pages = {pkab029},
year = {2021},
abstract = {Incidence of early-onset (younger than 50 years of age)
colorectal cancer (CRC) is increasing in many countries.
Thus, elucidating the role of traditional CRC risk factors
in early-onset CRC is a high priority. We sought to
determine whether risk factors associated with late-onset
CRC were also linked to early-onset CRC and whether
association patterns differed by anatomic subsite.Using data
pooled from 13 population-based studies, we studied 3767 CRC
cases and 4049 controls aged younger than 50 years and
23 437 CRC cases and 35 311 controls aged 50 years and
older. Using multivariable and multinomial logistic
regression, we estimated odds ratios (ORs) and $95\%$
confidence intervals (CIs) to assess the association between
risk factors and early-onset CRC and by anatomic
subsite.Early-onset CRC was associated with not regularly
using nonsteroidal anti-inflammatory drugs (OR = 1.43,
$95\%$ CI = 1.21 to 1.68), greater red meat intake (OR =
1.10, $95\%$ CI = 1.04 to 1.16), lower educational
attainment (OR = 1.10, $95\%$ CI = 1.04 to 1.16), alcohol
abstinence (OR = 1.23, $95\%$ CI = 1.08 to 1.39), and
heavier alcohol use (OR = 1.25, $95\%$ CI = 1.04 to 1.50).
No factors exhibited a greater excess in early-onset
compared with late-onset CRC. Evaluating risks by anatomic
subsite, we found that lower total fiber intake was linked
more strongly to rectal (OR = 1.30, $95\%$ CI = 1.14 to
1.48) than colon cancer (OR = 1.14, $95\%$ CI = 1.02 to
1.27; P = .04).In this large study, we identified several
nongenetic risk factors associated with early-onset CRC,
providing a basis for targeted identification of those most
at risk, which is imperative in mitigating the rising burden
of this disease.},
cin = {C070 / C120 / HD01 / C020},
ddc = {610},
cid = {I:(DE-He78)C070-20160331 / I:(DE-He78)C120-20160331 /
I:(DE-He78)HD01-20160331 / 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:34041438},
pmc = {pmc:PMC8134523},
doi = {10.1093/jncics/pkab029},
url = {https://inrepo02.dkfz.de/record/168982},
}