Key result
Metabolic-obesity phenotypes modify SYNTAX II scores and predicted CABG mortality, but not SYNTAX I.
Why the study?
BMI fails to capture underlying cardiometabolic heterogeneity in cardiovascular risk stratification. Whether metabolic–obesity phenotypes are associated with differences in coronary disease complexity and SYNTAX II-based revascularization risk remained incompletely defined.
Are metabolic–obesity phenotypes associated with differences in SYNTAX I, SYNTAX II scores, and predicted 4-year revascularization-related mortality in patients undergoing coronary angiography?
Cohort (n=270)
No
Are metabolic–obesity phenotypes associated with differences in SYNTAX I, SYNTAX II scores, and predicted 4-year revascularization-related mortality in patients undergoing coronary angiography?
Metabolic health status rather than BMI alone drives clinically integrated revascularization risk (SYNTAX II), identifying metabolically unhealthy non-obese patients as a high-risk group with higher predicted PCI- and CABG-related 4-year mortality compared to metabolically healthy non-obese patients.
Background Body mass index (BMI) is widely used for cardiovascular risk stratification, yet it fails to capture underlying cardiometabolic heterogeneity. Whether metabolic–obesity phenotypes are associated with differences in coronary disease complexity and revascularization risk remains incompletely defined. Objectives To evaluate the association between metabolic–obesity phenotypes and SYNTAX I, SYNTAX II scores, and predicted revascularization-related mortality. Methods In this retrospective single-center cohort study, 270 patients undergoing coronary angiography were classified into four metabolic–obesity phenotypes based on BMI (<30 or ≥30 kg/m²) and the presence of hypertension, diabetes mellitus, or dyslipidemia: metabolically healthy non-obese (MHNO), metabolically unhealthy non-obese (MUNO), metabolically healthy obese (MHO), and metabolically unhealthy obese (MUO). Anatomical disease complexity (SYNTAX I), clinically integrated risk assessment (SYNTAX II for PCI and CABG), and predicted 4-year mortality were compared across phenotypes using ANOVA with Tukey-adjusted post-hoc testing. Results Anatomical disease complexity assessed by SYNTAX I did not differ significantly among phenotypes (p=0.13). In contrast, SYNTAX II scores differed significantly for both PCI (p=0.013) and CABG (p=0.043). Predicted 4-year mortality following CABG also varied significantly across metabolic phenotypes (p=0.030), whereas EuroSCORE values were comparable (p=0.44). Tukey-adjusted pairwise analyses demonstrated that MUNO patients exhibited significantly higher SYNTAX II PCI scores and higher predicted PCI- and CABG-related 4-year mortality compared with MHNO patients, while no significant differences were observed among other phenotype pairs. Conclusions Metabolic health status, rather than BMI alone, is a key determinant of clinically integrated revascularization risk. Metabolically unhealthy non-obese patients represent a high-risk phenotype that may be underrecognized by BMI-based stratification. Incorporation of simple comorbidity-defined metabolic status may enhance Heart Team risk assessment and guide revascularization decision-making.
No takes yet. Share an insight, caveat, or question.
Fanne et al. (2026) conducted a cohort in Coronary artery disease undergoing coronary angiography (n=270). Metabolically unhealthy non-obese (MUNO) and other metabolic–obesity phenotypes vs. Metabolically healthy non-obese (MHNO) phenotype was evaluated on SYNTAX I, SYNTAX II scores (for PCI and CABG), and predicted 4-year revascularization-related mortality (p=0.013 for SYNTAX II PCI; 0.043 for SYNTAX II CABG; 0.030 for predicted 4-year CABG mortality). Metabolic–obesity phenotypes significantly modified SYNTAX II scores for PCI (p=0.013) and CABG (p=0.043) and predicted 4-year CABG mortality (p=0.030), but not SYNTAX I (p=0.13).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: