Background: Circulating bile acids (cBAs) function as signaling molecules that activate the farnesoid X receptor (FXR), promoting the secretion of fibroblast growth factor 19 (FGF-19), a gut-derived hormone involved in bile acid (BA) synthesis, glucose metabolism, and insulin sensitivity. However, the relationship between fasting cBAs, FGF-19, and insulin resistance—as estimated by HOMA-IR—remains unclear. This study explored these associations in an elderly population from Northern Italy.
Material and methods: We examined a subsample of 1080 subjects (aged 60–75 years, 1:1 male-to-female ratio) from the RoCAV population-based study (2013–2016). Fasting blood samples were analyzed for 33 cBAs using UHPLC-MS/MS, of which 23 met quality criteria. FGF-19 levels were also measured. After excluding individuals with missing data or fibrate therapy, 1049 participants were included. Associations between cBAs, FGF-19, and HOMA-IR were assessed via linear regression, adjusting for age, sex, BMI, diet, alcohol intake, hypertension, and dyslipidemia. ROC curve analysis evaluated the ability of cBAs and FGF-19 to discriminate T2DM cases.
Results: After excluding participants with missing anthropometric and clinical data or in fibrate treatment, data from 1049 subjects (mean±SD age 68.6±4.5 years, males 49.5%, T2DM 10.6%) were analysed. FGF-19 showed a positive correlation with primary cBAs (Spearman’s ρ=0.33, p<0.001). Adjusted for covariates, both primary and secondary cBAs were positively associated with HOMA-IR (β=0.07, p=5×10-5; β=0.9, p=4×10-7) while FGF-19 was not (β=-0.02, p=0.31). In the mutually-adjusted model - including primary and secondary cBAs, FGF-19, and covariates - the β coefficients for cBAs were attenuated but remained significant (primary: β=0.06, p=0.005; secondary: β=0.07, p=0.0003), and FGF-19 retained an inverse association (β=–0.05, p=0.009). When total cBAs were used in the FGF-19–adjusted model, the association with HOMA-IR was the strongest (β=0.19, p=5×10-19). ROC curve analysis indicated that the inclusion of primary and secondary cBAs and FGF-19 improved model discrimination for T2DM (ΔAUC=0.03, 95% Confidence Interval: 0.01-0.06; Net Reclassification Improvement=0.54; 95%CI: 0.30-0.75).
Conclusions: In this elderly Italian population, primary and secondary cBAs were positively associated with insulin resistance, after adjusting for each other, whereas FGF-19 negatively. These markers may enhance T2DM risk stratification and may give insights on bile acid–glucose metabolism links.
CORE (COnnecting REpositories)
CORE (COnnecting REpositories)