Key result
Sepsis-induced myocardial dysfunction in septic shock is linked to markedly higher myocardial glucose uptake.
Why the study?
Sepsis-induced myocardial dysfunction is common in septic shock, but its cardiac energy profile during contractile impairment remains poorly understood due to limited, largely invasive evidence.
Does sequential cardiac PET imaging reveal altered myocardial energy profiles in patients with sepsis-induced myocardial dysfunction compared to those without?
Cohort (n=24)
Unblinded
No
Does sequential cardiac PET imaging reveal altered myocardial energy profiles in patients with sepsis-induced myocardial dysfunction compared to those without?
Absolute Event Rate: 19.1% vs 1.3%
p-value: p=0.0071
In early septic shock, hearts with sepsis-induced myocardial dysfunction exhibit a metabolic shift characterized by increased glucose uptake and altered fatty acid utilization, which correlates with impaired myocardial efficiency.
Increased myocardial glucose uptake in SIMD may signal altered metabolism in septic shock; leaves open whether metabolic modulation affects outcomes in prospective trials.
Purpose Sepsis-induced myocardial dysfunction (SIMD) is common in septic shock (SS), but its cardiac energy profile in the context of contractile impairment remains poorly understood. Previous evidence is limited and largely based on invasive methods, suggesting reduced myocardial fatty acid and glucose utilization. Methods In this pilot, single-center, prospective observational study, patients were recruited within 48 hours of admission for circulatory shock and/or heart failure, and classified into three groups based on clinical history and early echocardiography: (i) SS with SIMD, (ii) SS without SIMD, and (iii) acute heart failure with reduced ejection fraction (AHFrEF) without SS. Sequential cardiac PET imaging was performed using three tracers (acetate, palmitate, and fluorodeoxyglucose [FDG]). The primary objective as a pilot study was to assess feasibility in generating preliminary signals of changing myocardial energy profiles between groups; secondary objectives included assessing cross-compensation of glucose and fatty acids in SS with SIMD and its association with contractile impairment. Results Twenty-four patients underwent PET imaging with kinetic analyses. Myocardial glucose uptake was significantly higher in SS with SIMD than without (median [IQR]: 19.1 [11.3–31.8] vs. 1.3 [0.1–4.0] μmol/100 g/min; p = 0.0071), and the uptake gap between fatty acids and glucose was narrowed in SS with SIMD compared with AHFrEF (p = 0.0168). Increased cardiac fatty acid esterification tended to correlate with low left ventricular ejection fraction (LVEF) in SS (Spearman’s rank r = −0.5189 (95%CI −0.8285- 0.0335); two-tailed p = 0.0597, n = 14). Myocardial oxygen consumption (MVO₂) was elevated in SS, and lower LVEF was associated with reduced myocardial efficiency (MEE) (r = 0.6221 [95%CI 0.1671–0.8586, p = 0.0118, n = 16). Conclusion In septic shock, hearts with contractile dysfunction increase glucose uptake/trapping and fatty acids are diverted toward a higher esterification fraction. This metabolic shift is associated with impaired myocardial efficiency, reflecting an imbalance between cardiac work and energy consumption. Trial registration This eMESH trial (NCT05202938) was prospectively registered at ClinicalTrials.gov on January 10th, 2022 prior to first patient inclusion.
No takes yet. Share an insight, caveat, or question.
Lesur et al. (2026) conducted a cohort in Septic shock with sepsis-induced myocardial dysfunction (n=24). Sepsis-induced myocardial dysfunction (SIMD) vs. Septic shock without SIMD was evaluated on Myocardial glucose uptake (μmol/100 g/min) (p=0.0071). Sepsis-induced myocardial dysfunction in septic shock patients was associated with significantly higher myocardial glucose uptake compared to septic shock without myocardial dysfunction (19.1 vs. 1.3 μmol/100 g/min, p=0.0071).
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: