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@ARTICLE{Guo:167753,
author = {F. Guo$^*$ and X. Chen$^*$ and J. Chang-Claude$^*$ and M.
Hoffmeister$^*$ and H. Brenner$^*$},
title = {{C}olorectal {C}ancer {R}isk by {G}enetic {V}ariants in
{P}opulations {W}ith and {W}ithout {C}olonoscopy {H}istory.},
journal = {JNCI cancer spectrum},
volume = {5},
number = {1},
issn = {2515-5091},
address = {Oxford},
publisher = {Oxford University Press},
reportid = {DKFZ-2021-00517},
pages = {pkab008},
year = {2021},
note = {#EA:C070#LA:C070#},
abstract = {Polygenic risk scores (PRS), which are derived from results
of large genome-wide association studies, are increasingly
propagated for colorectal cancer (CRC) risk stratification.
The majority of studies included in the large genome-wide
association studies consortia were conducted in the United
States and Germany, where colonoscopy with detection and
removal of polyps has been widely practiced over the last
decades. We aimed to assess if and to what extent the
history of colonoscopy with polypectomy may alter metrics of
the predictive ability of PRS for CRC risk.A PRS based on
140 single nucleotide polymorphisms was compared between
4939 CRC patients and 3797 control persons of the
Darmkrebs: Chancen der Verhütung durch Screening (DACHS)
study, a population-based case-control study conducted in
Germany. Risk discrimination was quantified according to the
history of colonoscopy and polypectomy by areas under the
curves (AUCs) and their $95\%$ confidence intervals (CIs).
All statistical tests were 2-sided.AUCs and $95\%$ CIs were
higher among subjects without previous colonoscopy (AUC =
0.622, $95\%$ CI = 0.606 to 0.639) than among those with
previous colonoscopy and polypectomy (AUC = 0.568, $95\%$ CI
= 0.536 to 0.601; difference [Δ AUC] = 0.054, P = .004).
Such differences were consistently seen in sex-specific
groups (women: Δ AUC = 0.073, P = .02; men: Δ AUC = 0.046,
P = .048) and age-specific groups (younger than 70 years: Δ
AUC = 0.052, P = .07; 70 years or older: Δ AUC = 0.049, P =
.045).Predictive performance of PRS may be underestimated in
populations with widespread use of colonoscopy. Future
studies using PRS to develop CRC prediction models should
carefully consider colonoscopy history to provide more
accurate estimates.},
cin = {C070 / C020},
ddc = {610},
cid = {I:(DE-He78)C070-20160331 / 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:33644683},
pmc = {pmc:PMC7898082},
doi = {10.1093/jncics/pkab008},
url = {https://inrepo02.dkfz.de/record/167753},
}