TY - JOUR
AU - Hua, Xinwei
AU - Dai, James Y
AU - Lindström, Sara
AU - Harrison, Tabitha A
AU - Lin, Yi
AU - Alberts, Steven R
AU - Alwers, Elizabeth
AU - Berndt, Sonja I
AU - Brenner, Hermann
AU - Buchanan, Daniel D
AU - Campbell, Peter T
AU - Casey, Graham
AU - Chang-Claude, Jenny
AU - Gallinger, Steven
AU - Giles, Graham G
AU - Goldberg, Richard M
AU - Gunter, Marc J
AU - Hoffmeister, Michael
AU - Jenkins, Mark A
AU - Joshi, Amit D
AU - Ma, Wenjie
AU - Milne, Roger L
AU - Murphy, Neil
AU - Pai, Rish K
AU - Sakoda, Lori C
AU - Schoen, Robert E
AU - Shi, Qian
AU - Slattery, Martha L
AU - Song, Mingyang
AU - White, Emily
AU - Le Marchand, Loic
AU - Chan, Andrew T
AU - Peters, Ulrike
AU - Newcomb, Polly A
TI - Genetically predicted circulating C-reactive protein concentration and colorectal cancer survival: A Mendelian randomization consortium study.
JO - Cancer epidemiology, biomarkers & prevention
VL - 30
IS - 7
SN - 1538-7755
CY - Philadelphia, Pa.
PB - AACR
M1 - DKFZ-2021-01065
SP - 1349-1358
PY - 2021
N1 - 2021 Jul;30(7):1349-1358
AB - A positive association between circulating C-reactive protein (CRP) and colorectal cancer (CRC) survival was reported in observational studies, which are susceptible to unmeasured confounding and reverse causality. We used a Mendelian randomization approach to evaluate the association between genetically-predicted CRP concentrations and CRC-specific survival.We used individual-level data for 16,918 eligible CRC cases of European ancestry from 15 studies within the International Survival Analysis of Colorectal Cancer Consortium. We calculated a genetic risk score based on 52 CRP-associated genetic variants identified from genome-wide association studies. Due to the non-collapsibility of hazard ratios from Cox proportional hazards models, we used the additive hazards model to calculate hazard differences (HD) and 95
LB - PUB:(DE-HGF)16
C6 - pmid:33972368
DO - DOI:10.1158/1055-9965.EPI-20-1848
UR - https://inrepo02.dkfz.de/record/168784
ER -