To denoise and handle censoring, we applied Principal Component Pursuit with LOD adjustment (PCP-LOD), decomposing the exposure matrix into a non-negative low-rank component (population co-exposure profiles) and a sparse component (individual spikes), and then used Bayesian Kernel Machine Regression (BKMR) to estimate nonlinear and interactive associations with AST, ALT, GGT, ALP, total bilirubin, and the Fatty Liver Index (FLI), retaining analytes with ≥50% detection. This evidence concerns the gene GPT and fatty liver disease.