Use of circulating microRNAs to identify high-risk adenomas among FIT+ patients undergoing screening colonoscopy.

BACKGROUND

Colonoscopy prevents colorectal cancer (CRC) but is invasive and resource intensive. Circulating microRNAs (miRNAs) may improve risk stratification of fecal immunochemical test (FIT)-positive individuals by identifying high-risk adenomas (HRAs). We evaluated the association of circulating miRNAs with HRAs and their contribution to risk prediction models (RPMs).

METHODS

We analyzed 398 FIT-positive participants from a Canadian screening cohort (160 HRAs; 238 controls). Plasma miRNAs were quantified using NanoString nCounter. Differential expression was assessed using two-tailed t-tests with Bonferroni correction, and LASSO regression identified predictive miRNAs. Five RPMs were developed (Baseline, Bonferroni, Bonferroni+Baseline, LASSO, LASSO+Baseline) and evaluated using AUCs, DeLong's test, calibration, bootstrap validation, and decision curve analysis.

RESULTS

Eleven miRNAs were Bonferroni-significant, and LASSO retained 8 predictors. The Baseline model had an optimism-corrected AUC of 0.61, increasing to 0.80 with these miRNAs and 0.82 with baseline variables added; the LASSO+Baseline model achieved an AUC of 0.82 with good calibration. All miRNA-enhanced models outperformed Baseline (P<0.001) and showed greater net benefit on decision curve analysis. At a 20% threshold, the LASSO+Baseline model achieved 95.0% sensitivity and 56.7% PPV. Conclusions Circulating miRNAs substantially improved identification of HRAs among FIT-positive individuals with clinical utility.

IMPACT: These data support further evaluation of miRNA-informed RPMs to refine CRC screening.