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@ARTICLE{Murphy:182833,
author = {N. Murphy and C. C. Newton and M. Song and N. Papadimitriou
and M. Hoffmeister$^*$ and A. I. Phipps and T. A. Harrison
and P. A. Newcomb and E. K. Aglago and S. I. Berndt and H.
Brenner$^*$ and D. D. Buchanan and Y. Cao and A. T. Chan and
X. Chen$^*$ and I. Cheng and J. Chang-Claude$^*$ and N.
Dimou and D. Drew and A. B. Farris and A. J. French and S.
Gallinger and P. Georgeson and M. Giannakis and G. G. Giles
and S. B. Gruber and S. Harlid and L. Hsu and W.-Y. Huang
and M. A. Jenkins and R. S. Laskar and L. Le Marchand and P.
Limburg and Y. Lin and M. Mandic$^*$ and J. A. Nowak and M.
Obón-Santacana and S. Ogino and C. Qu and L. C. Sakoda and
R. E. Schoen and M. C. Southey and Z. K. Stadler and R. S.
Steinfelder and W. Sun and S. N. Thibodeau and A. E. Toland
and Q. M. Trinh and K. K. Tsilidis and T. Ugai and B. Van
Guelpen and X. Wang and M. O. Woods and S. H. Zaidi and M.
J. Gunter and U. Peters and P. T. Campbell},
title = {{B}ody {M}ass {I}ndex and {M}olecular {S}ubtypes of
{C}olorectal {C}ancer.},
journal = {Journal of the National Cancer Institute},
volume = {115},
number = {2},
issn = {0027-8874},
address = {Oxford},
publisher = {Oxford Univ. Press},
reportid = {DKFZ-2022-02960},
pages = {165-173},
year = {2023},
note = {2023 Feb 8;115(2):165-173},
abstract = {Obesity is an established risk factor for colorectal cancer
(CRC); but the evidence for the association is inconsistent
across molecular subtypes of the disease.We pooled data on
BMI, tumor microsatellite instability (MSI) status, CpG
island methylator phenotype (CIMP) status, BRAF and KRAS
mutations, and Jass classification types for 11,872 CRC
cases and 11,013 controls from 11 observational studies. We
used multinomial logistic regression to estimate odds ratio
(OR) and $95\%$ confidence intervals (CI) adjusted for
covariables.Higher BMI was associated with increased CRC
risk (OR per 5 kg/m2, 1.18, $95\%CI:$ 1.15-1.22). The
positive association was stronger for men than women, but
similar across tumor subtypes defined by individual
molecular markers. In analyses by Jass type, higher BMI was
associated with elevated CRC risk for types 1-4 cases but
not for type 5 CRC cases (considered familial-like/Lynch
syndrome MSI-H, CIMP-low/negative, BRAF-wildtype,
KRAS-wildtype, OR, 1.04, $95\%CI:$ 0.90-1.20). This pattern
of associations for BMI and Jass types was consistent by sex
and design of contributing studies (cohort or
case-control).In contrast to previous reports with fewer
study participants, we found limited evidence of
heterogeneity for the association between BMI and CRC risk
according to molecular subtype, suggesting that obesity
influences nearly all major pathways involved in colorectal
carcinogenesis. The null association observed for the Jass
type 5 suggests that BMI is not a risk factor for the
development of CRC for individuals with Lynch syndrome.},
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:36445035},
doi = {10.1093/jnci/djac215},
url = {https://inrepo02.dkfz.de/record/182833},
}