The Association between Genetically Predicted C-Reactive Protein Levels and Risk of Colorectal Cancer in an East Asian Population: Two-Sample Mendelian Randomization.
[BACKGROUND] C-reactive protein (CRP) is a widely used inflammatory biomarker that has been related to colorectal cancer risk.
APA
Choi CK, Yang JH, et al. (2026). The Association between Genetically Predicted C-Reactive Protein Levels and Risk of Colorectal Cancer in an East Asian Population: Two-Sample Mendelian Randomization.. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 35(2), 348-350. https://doi.org/10.1158/1055-9965.EPI-25-1230
MLA
Choi CK, et al.. "The Association between Genetically Predicted C-Reactive Protein Levels and Risk of Colorectal Cancer in an East Asian Population: Two-Sample Mendelian Randomization.." Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, vol. 35, no. 2, 2026, pp. 348-350.
PMID
41236733
Abstract
[BACKGROUND] C-reactive protein (CRP) is a widely used inflammatory biomarker that has been related to colorectal cancer risk. However, observational studies are prone to confounding and reverse causality.
[METHODS] We conducted a two-sample Mendelian randomization using CRP genome-wide association study (GWAS) data from 59,605 Korean individuals and colorectal cancer GWAS data from 23,572 cases and 48,700 controls from an East Asia population. The analysis had 80% power to detect an OR of 1.12 for colorectal cancer risk per twofold increase in CRP levels.
[RESULTS] Genetically predicted serum CRP levels (per twofold increase) were not significantly associated with colorectal cancer risk (inverse-variance weighted OR, 0.995; 95% confidence interval, 0.893-1.109; P value, 0.929). Null findings remained consistent in sensitivity analyses excluding the horizontally pleiotropic effect.
[CONCLUSIONS] Despite sufficient statistical power, little evidence supported a causal association between CRP and colorectal cancer risk in East Asians.
[IMPACT] Our findings suggest that CRP is unlikely to be a key determinant of colorectal carcinogenesis, aligning with prior studies in European populations.
[METHODS] We conducted a two-sample Mendelian randomization using CRP genome-wide association study (GWAS) data from 59,605 Korean individuals and colorectal cancer GWAS data from 23,572 cases and 48,700 controls from an East Asia population. The analysis had 80% power to detect an OR of 1.12 for colorectal cancer risk per twofold increase in CRP levels.
[RESULTS] Genetically predicted serum CRP levels (per twofold increase) were not significantly associated with colorectal cancer risk (inverse-variance weighted OR, 0.995; 95% confidence interval, 0.893-1.109; P value, 0.929). Null findings remained consistent in sensitivity analyses excluding the horizontally pleiotropic effect.
[CONCLUSIONS] Despite sufficient statistical power, little evidence supported a causal association between CRP and colorectal cancer risk in East Asians.
[IMPACT] Our findings suggest that CRP is unlikely to be a key determinant of colorectal carcinogenesis, aligning with prior studies in European populations.
MeSH Terms
Humans; Colorectal Neoplasms; C-Reactive Protein; Mendelian Randomization Analysis; Genome-Wide Association Study; Risk Factors; Male; Female; Asian People; Case-Control Studies; Republic of Korea; Asia, Eastern; Biomarkers, Tumor; Polymorphism, Single Nucleotide; East Asian People