Key result
Discordant low subendocardial myocardial flow reserve is linked to ~41% higher MACE risk.
Why the study?
Although reduced subendocardial flows predict adverse outcomes, the incremental value of subendocardial MFR beyond transmural MFR remained unclear.
Does subendocardial myocardial flow reserve assessment improve risk stratification for major adverse cardiovascular events in patients with normal perfusion and preserved transmural flow reserve?
Cohort (n=6,603)
Yes
Does subendocardial myocardial flow reserve assessment improve risk stratification for major adverse cardiovascular events in patients with normal perfusion and preserved transmural flow reserve?
Layer-specific PET myocardial perfusion analysis identifies a significant subgroup of patients with isolated subendocardial flow impairment who are at 1.4-fold higher risk for adverse cardiovascular events despite conventionally 'normal' transmural flow reserve.
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Subendocardial MFR may refine risk stratification beyond transmural measures; hypothesis-generating and should not yet change practice.
BACKGROUND: Although the prognostic utility of positron emission tomography (PET) myocardial flow reserve (MFR) is well established, emerging data suggest that reduced subendocardial flows also predict adverse outcomes. However, the incremental value of subendocardial MFR (MFR SE ) beyond transmural MFR (MFR TM ) remains unclear. METHODS: We studied patients in a multicenter PET registry with normal perfusion on stress/rest Rb-82 PET, excluding those with a previous history of coronary artery bypass surgery, heart transplantation, or left ventricular ejection fraction <40%. The optimal MFR SE cutoff for predicting major adverse cardiovascular events (MACEs; death, myocardial infarction [MI], revascularization, or heart failure [HF] hospitalization) was determined using Youden’s index. Patients were stratified into 3 groups: concordant-normal (MFR TM ≥2.0; MFR SE ≥2.1), discordant (low-MFR SE , normal MFR TM ), and abnormal MFR TM . Clinical outcomes were compared by MFR groups. RESULTS: Among 6603 patients (normal N=4103; discordant N=885; abnormal N=1615) the mean age was 66.3±12.4 years, and 54% were women. Compared with the concordant-normal group, patients with discordant low-MFR SE were older and more likely to have hypertension, diabetes, peripheral artery disease, and previous percutaneous coronary intervention. The median MFR TM for normal, discordant, and abnormal groups were 2.86, 2.15, and 1.72, respectively. Over a m edian follow-up of 4.9 years, 1661 MACE events occurred. Discordant low-MFR SE patients had a higher risk of MACE (hazard ratio [HR], 1.41; 95% CI, 1.22–1.64) and all-cause mortality (HR, 1.36; 95% CI, 1.14–1.61) compared with concordant-normal patients. The discordant group had an intermediate absolute risk of MACE, with an adjusted annualized event rate of 5.79% (95% CI, 5.10–6.49) compared with 3.99% (95% CI, 3.67–4.30; P <0.001) in the concordant-normal group and 8.35% (95% CI, 7.71–9.00; P <0.001) in the abnormal MFR TM group. CONCLUSIONS: Subendocardial MFR reveals clinically meaningful risk heterogeneity among patients with preserved transmural flow reserve, helping refine risk stratification beyond traditional PET metrics.
Lopez et al. (2026) conducted a cohort in Normal myocardial perfusion without overt obstructive coronary artery disease (n=6,603). Discordant low subendocardial myocardial flow reserve (MFR SE <2.1) vs. Concordant-normal flow reserve (MFR TM ≥2.0 and MFR SE ≥2.1) was evaluated on Major adverse cardiovascular events (MACE: composite of all-cause death, non-fatal MI, heart failure hospitalization, or late coronary revascularization) (HR 1.41, 95% CI 1.22-1.64, p=<0.001). Patients with discordant low subendocardial myocardial flow reserve despite preserved transmural flow had a higher risk of MACE (HR 1.41) compared to those with concordant normal flow.
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