Threshold effect analysis of TS on mortality.

BackgroundTransferrin saturation (TS) is associated with mortality across populations, but its nonlinear relationship with all-cause mortality in coronary artery disease (CAD) and the role of systemic inflammation remain unclear. This study explored the association between TS and mortality in CAD patients, focusing on systemic inflammation as a potential mediator.MethodsData from National Health and Nutrition Examination Survey (NHANES) 1999–2006 included 769 CAD patients (>18 years) with available TS and mortality records. Systemic inflammation markers, such as the systemic immune-inflammation index (SII) and systemic inflammation response index (SIRI), were analyzed. Kaplan–Meier curves, Cox proportional hazards models, and mediation analyses examined the interactions between TS, inflammation, and mortality.ResultsA U-shaped relationship between TS and all-cause mortality was observed, with an inflection point at 30.5%. TS levels ≤30.5% were inversely associated with mortality (HR = 0.98; 95% CI, 0.96–0.99; P 30.5% increased mortality risk (HR = 1.05; 95% CI, 1.02–1.08; P 30.5%.ConclusionsTS demonstrates a U-shaped relationship with all-cause mortality in CAD patients. Systemic inflammation is linked to both TS and mortality outcomes, suggesting potential mechanistic interplay. Maintaining TS within 20–30% and addressing inflammation may reduce mortality risk.