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@ARTICLE{Harbs:179436,
author = {J. Harbs and S. Rinaldi and A. Gicquiau and P.
Keski-Rahkonen and N. Mori and X. Liu and R. Kaaks$^*$ and
V. Katzke$^*$ and M. B. Schulze and C. Agnoli and R. Tumino
and B. Bueno-de-Mesquita and M. Crous-Bou and M.-J. Sánchez
and A. Aizpurua and M.-D. Chirlaque and A. B. Gurrea and R.
C. Travis and E. L. Watts and S. Christakoudi and K. K.
Tsilidis and E. Weiderpass and M. J. Gunter and B. Van
Guelpen and N. Murphy and S. Harlid},
title = {{C}irculating {S}ex {H}ormone {L}evels and {C}olon {C}ancer
{R}isk in {M}en: {A} {N}ested {C}ase-{C}ontrol {S}tudy and
{M}eta-{A}nalysis.},
journal = {Cancer epidemiology, biomarkers $\&$ prevention},
volume = {31},
number = {4},
issn = {1055-9965},
address = {Philadelphia, Pa.},
publisher = {AACR},
reportid = {DKFZ-2022-00676},
pages = {793 - 803},
year = {2022},
abstract = {Endogenous sex hormones may contribute to higher colorectal
cancer incidence rates in men compared with women, but
despite an increased number of studies, clear evidence is
lacking.We conducted a comprehensive nested case-control
study of circulating concentrations of sex hormones, sex
hormone precursors, and sex hormone binding globulin (SHBG)
in relation to subsequent colon cancer risk in European men.
Concentrations were measured using liquid LC/MS-MS in
prospectively collected plasma samples from 690 cases and
690 matched controls from the European Prospective
Investigation into Cancer and Nutrition (EPIC) and the
Northern Sweden Health and Disease Study (NSHDS) cohorts.
Multivariable conditional logistic regression was used to
estimate odds ratios (OR) and $95\%$ confidence intervals
(CI). In addition, we conducted a meta-analysis of previous
studies on men.Circulating levels of testosterone (OR, 0.68;
$95\%$ CI, 0.51-0.89) and SHBG (OR, 0.77; $95\%$ CI,
0.62-0.96) were inversely associated with colon cancer risk.
For free testosterone, there was a nonsignificant inverse
association (OR, 0.83; $95\%$ CI, 0.58-1.18). In a
dose-response meta-analysis of endogenous sex hormone
levels, inverse associations with colorectal/colon cancer
risk were found for testosterone [relative risks (RR) per
100 ng/dL = 0.98; $95\%$ CI, 0.96-1.00; I2 = $22\%]$ and
free testosterone (RR per 1 ng/dL = 0.98; $95\%$ CI,
0.95-1.00; I2 = $0\%).Our$ results provide suggestive
evidence for the association between testosterone, SHBG, and
male colon cancer development.Additional support for the
involvement of sex hormones in male colon cancer.},
keywords = {Case-Control Studies / Colonic Neoplasms: epidemiology /
Estradiol / Female / Gonadal Steroid Hormones / Humans /
Logistic Models / Male / Prospective Studies / Risk Factors
/ Sex Hormone-Binding Globulin: metabolism / Testosterone /
Gonadal Steroid Hormones (NLM Chemicals) / Sex
Hormone-Binding Globulin (NLM Chemicals) / Testosterone (NLM
Chemicals) / Estradiol (NLM Chemicals)},
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:35086823},
doi = {10.1158/1055-9965.EPI-21-0996},
url = {https://inrepo02.dkfz.de/record/179436},
}