Key result
Higher TyG index is linked to an ~4-fold higher risk of post-STEMI coronary microvascular dysfunction.
Why the study?
Metabolic dysfunction and inflammation may jointly contribute to coronary microvascular injury and adverse outcomes after PPCI for STEMI, but their independent and combined associations with AMR-defined CMD and 12-month MACE remain unclear.
Cohort (n=318)
No
May aid post-STEMI risk stratification; leaves open prospective validation before clinical adoption.
Background: Metabolic dysfunction and inflammation may jointly contribute to coronary microvascular injury and adverse outcomes after primary percutaneous coronary intervention (PPCI) for ST-segment elevation myocardial infarction (STEMI). We examined the independent and combined associations of the triglyceride-glucose (TyG) index and inflammatory burden index (IBI) with angiographic microvascular resistance (AMR)-defined coronary microvascular dysfunction (CMD), their incremental value beyond conventional factors, and their associations with 12-month major adverse cardiovascular events (MACE). Methods: In this retrospective cohort study conducted at a single center, 318 STEMI patients who underwent PPCI and achieved a TIMI grade 3 flow post-procedure were enrolled. AMR was derived from the final post-PPCI angiogram of the culprit vessel, and CMD was defined as AMR >26.6 mmHg·s/dm. Multivariable models assessed associations with CMD and MACE. Sequential models evaluated the incremental performance of TyG and IBI with 1,000-resample bootstrap internal validation. Results: CMD was present in 102/318 (32.1%). TyG (OR per 1-unit, 3.83; 95% CI, 2.04-7.21; P<0.001) and IBI (OR per 10-units, 1.13; 95% CI, 1.07-1.20; P<0.001) were independently associated with CMD. The TyG-IBI model showed an AUC of 0.773 for CMD; adding both to a clinical/procedural model improved the AUC from 0.904 to 0.939 (bootstrap-validated, 0.920; ΔAUC, 0.036; P = 0.001). Over 12 months, 69 (21.7%) patients had MACE. TyG (HR, 1.97; 95% CI, 1.30-2.98; P = 0.001) and IBI (HR per 10-units, 1.02; 95% CI, 1.00-1.05; P = 0.022) remained independent predictors of MACE, with the highest risk in those with both markers elevated. Conclusion: TyG and IBI were independently associated with AMR-defined CMD and 12-month MACE after STEMI. Adding TyG and IBI to conventional clinical and procedural factors improved model discrimination for CMD, although prospective multicenter validation is required before clinical application.
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Yang et al. (2026) conducted a cohort in ST-segment elevation myocardial infarction (STEMI) (n=318). Triglyceride-glucose (TyG) index and Inflammatory burden index (IBI) vs. Lower TyG index and IBI levels was evaluated on Coronary microvascular dysfunction (CMD) defined by angiographic microvascular resistance (AMR > 26.6 mmHg·s/dm) (OR 3.83, 95% CI 2.04-7.21, p=<0.001). Elevated TyG index (OR 3.83 per 1-unit increase) and inflammatory burden index (OR 1.13 per 10-unit increase) were independently associated with AMR-defined coronary microvascular dysfunction after STEMI.
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