In a cross-sectional study, we measured fasting levels of glucose, insulin, hemoglobin A1c, and C-peptide and calculated homeostatic model assessment (HOMA) values (used to quantify insulin resistance) for 19,361 asymptomatic South Korean subjects who underwent colonoscopy examinations from January 2006 to June 2009. Participants completed a standardized self-administered health questionnaire and a validated semiquantitative food frequency questionnaire. Blood samples were collected on the day of the colonoscopy; fasting blood samples were also collected. Robust Poisson regression was used to model the associations of glucose markers with the prevalence of any adenoma.
Using detailed multivariable-adjusted dose-response models, the prevalence ratios (aPR, 95% confidence interval [CI]) for any adenoma, comparing the 90th with the 10th percentile, were 1.08 (1.00–1.16; P = .04) for fasting glucose, 1.07 (0.99–1.15; P = .10) for insulin, 1.09 (1.02–1.18, P = .02) for HOMA, 1.09 (1.01–1.17; P = .02) for hemoglobin A1c, and 1.14 (1.05–1.24; P = .002) for C-peptide. The corresponding ratios for nonadvanced adenomas were 1.11 (0.99–1.25; P = .08), 1.10 (0.98–1.24; P = .12), 1.15 (1.02–1.29; P = .02), 1.14 (1.01–1.28; P = .03), and 1.20 (1.05–1.37; P = .007), respectively. The corresponding ratios for advanced adenomas were 1.32 (0.94–1.84; P = .11), 1.23 (0.87–1.75; P = .24), 1.30 (0.92–1.85; P = .14), 1.13 (0.79–1.61; P = .50), and 1.67 (1.15–2.42; P = .007), respectively. Metabolic syndrome was associated with the prevalence of any adenoma (aPR, 1.18; 95% CI, 1.13–1.24; P < .001), nonadvanced adenoma (aPR, 1.30; 95% CI, 1.20–1.40; P < .001), and advanced adenoma (aPR, 1.42; 95% CI, 1.14–1.78; P = .002). Associations were similar for adenomas located in the distal versus proximal colon.
Increasing levels of glucose, HOMA values, levels of hemoglobin A1c and C-peptide, and metabolic syndrome are significantly associated with the prevalence of adenomas. Adenomas should be added to the list of consequences of altered glucose metabolism.