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@ARTICLE{Khn:144635,
author = {T. Kühn$^*$ and M. Stepien and M. López-Nogueroles and A.
D. Machado$^*$ and D. Sookthai$^*$ and T. Johnson$^*$ and M.
Roca and A. Hüsing$^*$ and S. G. Maldonado and A. J. Cross
and N. Murphy and H. Freisling and S. Rinaldi and A.
Scalbert and V. Fedirco and G. Severi and M.-C.
Boutron-Ruault and F. R. Mancini and S. A. Sowah$^*$ and H.
Boeing and P. Jakszyn and M.-J. Sánchez and S. Merino and
S. Colorado-Yohar and A. Barricarte and K. T. Khaw and J. A.
Schmidt and A. Perez-Cornago and A. Trichopoulou and A.
Karakatsani and P. Thriskos and D. Palli and C. Agnoli and
R. Tumino and C. Sacerdote and S. Panico and B.
Bueno-de-Mesquita and C. H. van Gils and A. Heath and M. J.
Gunter and E. Riboli and A. Lahoz and M. Jenab and R.
Kaaks$^*$},
title = {{P}re-diagnostic plasma bile acid levels and colon cancer
risk: {A} prospective study.},
journal = {Journal of the National Cancer Institute},
volume = {112},
number = {5},
issn = {1460-2105},
address = {Oxford},
publisher = {Oxford Univ. Press},
reportid = {DKFZ-2019-02077},
pages = {516-524},
year = {2020},
note = {2020 May 1;112(5):516-524#EA:C020#LA:C020#},
abstract = {Bile acids have been proposed to promote colon
carcinogenesis. However, there are limited prospective data
on circulating bile acid levels and colon cancer risk in
humans.Associations between pre-diagnostic plasma levels of
17 primary, secondary and tertiary bile acid metabolites
(conjugated and unconjugated) and colon cancer risk were
evaluated in a nested case-control study within the European
Prospective Investigation into Cancer and Nutrition (EPIC)
cohort. Bile acid levels were quantified by tandem mass
spectrometry in samples from 569 incident colon cancer cases
and 569 matched controls. Multivariable logistic regression
analyses were used to estimate odds ratios (ORs) for colon
cancer risk across quartiles of bile acid
concentrations.Positive associations were observed between
colon cancer risk and plasma levels of 7 conjugated bile
acid metabolites, i.e. primary bile acids glycocholic acid
(ORQuartile 4 vs. Quartile 1=2.22,95 $\%$ confidence
interval[CI]=1.52, 3.26), taurocholic acid (OR = 1.78,
$95\%CI=1.23,$ 2.58), glycochenodeoxycholic acid
(OR = 1.68, $95\%CI=1.13,$ 2.48), taurochenodeoxycholic
acid (OR = 1.62, $95\%CI=1.11-2.36),$ and glycohyocholic
acid (OR = 1.65, $95\%CI=1.13,$ 2.40) as well as the
secondary bile acids glycodeoxycholic acid (OR = 1.68,
$95\%CI=1.12,$ 2.54) and taurodeoxycholic acid
(OR = 1.54, $95\%CI=1.02,$ 2.31). By contrast,
unconjugated bile acids and tertiary bile acids were not
associated with risk.This prospective study showed that
pre-diagnostic levels of certain conjugated primary and
secondary bile acids were positively associated with risk of
colon cancer. Our findings support experimental data to
suggest that a high bile acid load is colon cancer
promotive.},
cin = {C020},
ddc = {610},
cid = {I:(DE-He78)C020-20160331},
pnm = {313 - Cancer risk factors and prevention (POF3-313)},
pid = {G:(DE-HGF)POF3-313},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:31435679},
doi = {10.1093/jnci/djz166},
url = {https://inrepo02.dkfz.de/record/144635},
}