Key result
Accelerated physiologic aging linked to ~372% higher MACE risk in patients with abnormal endothelial function.
Why the study?
An AI algorithm detecting age from the 12-lead ECG may reflect physiologic age, but its association with vascular aging assessed by peripheral microvascular endothelial function remained to be investigated.
Is accelerated physiologic aging assessed by ECG-derived artificial intelligence associated with peripheral endothelial dysfunction and increased risk of major adverse cardiovascular events?
Observational (n=531)
Is accelerated physiologic aging assessed by ECG-derived artificial intelligence associated with peripheral endothelial dysfunction and increased risk of major adverse cardiovascular events?
Effect estimate: HR 4.72 (95% CI 1.24–17.91)
p-value: p=0.02
Accelerated physiologic aging assessed by an AI-ECG algorithm, combined with peripheral endothelial dysfunction, identifies patients at a markedly increased risk for major adverse cardiovascular events.
May aid identification of high-risk patients with endothelial dysfunction; leaves open prospective validation of AI-ECG aging.
Background An artificial intelligence algorithm that detects age using the 12‐lead ECG has been suggested to signal “physiologic age.” This study aimed to investigate the association of peripheral microvascular endothelial function (PMEF) as an index of vascular aging, with accelerated physiologic aging gauged by ECG‐derived artificial intelligence–estimated age. Methods and Results This study included 531 patients who underwent ECG and a noninvasive PMEF assessment using reactive hyperemia peripheral arterial tonometry. Abnormal PMEF was defined as reactive hyperemia peripheral arterial tonometry index ≤2.0. Accelerated or delayed physiologic aging was calculated by the Δ age (ECG‐derived artificial intelligence–estimated age minus chronological age), and the association between Δ age and PMEF as well as its impact on composite major adverse cardiovascular events were investigated. Δ age was higher in patients with abnormal PMEF than in patients with normal PMEF (2.3±7.8 versus 0.5±7.7 years; P =0.01). Reactive hyperemia peripheral arterial tonometry index was negatively associated with Δ age after adjustment for cardiovascular risk factors (standardized β coefficient, –0.08; P =0.048). The highest quartile of Δ age was associated with an increased risk of major adverse cardiovascular events compared with the first quartile of Δ age in patients with abnormal PMEF, even after adjustment for cardiovascular risk factors (hazard ratio, 4.72; 95% CI, 1.24–17.91; P =0.02). Conclusions Vascular aging detected by endothelial function is associated with accelerated physiologic aging, as assessed by the artificial intelligence–ECG Δ age. Patients with endothelial dysfunction and the highest quartile of accelerated physiologic aging have a marked increase in risk for cardiovascular events.
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Toya et al. (2021) conducted an observational in Patients undergoing ECG and peripheral microvascular endothelial function assessment (n=531). Accelerated physiologic aging (highest quartile of Δ age) and abnormal endothelial function vs. Lowest quartile of Δ age and normal endothelial function was evaluated on Composite major adverse cardiovascular events (MACE) (HR 4.72, 95% CI 1.24–17.91, p=0.02). Accelerated physiologic aging (highest vs lowest quartile) increased the risk of major adverse cardiovascular events in patients with abnormal endothelial function (HR 4.72; 95% CI 1.24–17.91; P=0.02).
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