Pre-diagnostic C-reactive protein concentrations, CRP genetic variation and mortality among individuals with colorectal cancer in Western European populations

Author:

Nimptsch KatharinaORCID,Aleksandrova Krasimira,Fedirko Veronika,Jenab Mazda,Gunter Marc J.,Siersema Peter D.,Wu Kana,Katzke Verena,Kaaks Rudolf,Panico Salvatore,Palli Domenico,May Anne M,Sieri Sabina,Bueno-de-Mesquita Bas,Standahl Karina,Sánchez Maria-Jose,Perez-Cornago Aurora,Olsen Anja,Tjønneland Anne,Bonet Catalina Bonet,Dahm Christina C.,Chirlaque María-Dolores,Fiano Valentina,Tumino Rosario,Gurrea Aurelio Barricarte,Boutron-Ruault Marie-Christine,Menegaux Florence,Severi Gianluca,van Guelpen Bethany,Lee Young-Ae,Pischon Tobias

Abstract

Abstract Background The role of elevated pre-diagnostic C-reactive protein (CRP) concentrations on mortality in individuals with colorectal cancer (CRC) remains unclear. Methods We investigated the association between pre-diagnostic high-sensitivity CRP concentrations and CRP genetic variation associated with circulating CRP and CRC-specific and all-cause mortality based on data from 1,235 individuals with CRC within the European Prospective Investigation into Cancer and Nutrition cohort using multivariable-adjusted Cox proportional hazards regression. Results During a median follow-up of 9.3 years, 455 CRC-specific deaths were recorded, out of 590 deaths from all causes. Pre-diagnostic CRP concentrations were not associated with CRC-specific (hazard ratio, HR highest versus lowest quintile 0.92, 95% confidence interval, CI 0.66, 1.28) or all-cause mortality (HR 0.91, 95% CI 0.68, 1.21). Genetic predisposition to higher CRP (weighted score based on alleles of four CRP SNPs associated with higher circulating CRP) was not significantly associated with CRC-specific mortality (HR per CRP-score unit 0.95, 95% CI 0.86, 1.05) or all-cause mortality (HR 0.98, 95% CI 0.90, 1.07). Among four investigated CRP genetic variants, only SNP rs1205 was significantly associated with CRC-specific (comparing the CT and CC genotypes with TT genotype, HR 0.54, 95% CI 0.35, 0.83 and HR 0.58, 95% CI 0.38, 0.88, respectively) and all-cause mortality (HR 0.58, 95% CI 0.40, 0.85 and 0.64, 95% CI 0.44, 0.92, respectively). Conclusions The results of this prospective cohort study do not support a role of pre-diagnostic CRP concentrations on mortality in individuals with CRC. The observed associations with rs1205 deserve further scientific attention.

Funder

Max-Delbrück-Centrum für Molekulare Medizin in der Helmholtz-Gemeinschaft (MDC)

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics,Oncology

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