Key result
Microvascular endothelial dysfunction (reactive hyperemia peripheral arterial tonometry index ≤2.0) predicted incident solid-tumor cancer (9.5% vs 3.7%; adjusted HR 2.52, 95% CI 1.17-5.45; p=0.019).
Why the study?
Microvascular endothelial dysfunction predicts cardiovascular adverse events, but its predictive value for the future risk of solid-tumor cancer had not been characterized.
Does microvascular endothelial dysfunction predict the future risk of solid-tumor cancer in patients undergoing peripheral arterial tonometry?
Cohort (n=488)
Does microvascular endothelial dysfunction predict the future risk of solid-tumor cancer in patients undergoing peripheral arterial tonometry?
Microvascular endothelial dysfunction is associated with a greater than two-fold increased risk of future solid-tumor cancer, suggesting its potential utility as a predictive marker beyond cardiovascular disease.
Answers are grounded in this paper and cite their sources.
Microvascular dysfunction may flag higher cancer risk; hypothesis-generating and needs prospective confirmation before clinical use.
Aims Cardiovascular health metrics predict the risk not only of cardiovascular diseases but also of several types of cancers. Microvascular endothelial dysfunction can predict future cardiovascular adverse events, but the predictive value of microvascular endothelial dysfunction for future risk of solid-tumor cancer has not been characterized. Methods A total of 488 patients who underwent microvascular endothelial function assessment using reactive hyperemia peripheral arterial tonometry were included in this study. Microvascular endothelial dysfunction was defined as a reactive hyperemia peripheral arterial tonometry index ≤2.0. Results Of 221 patients with a baseline reactive hyperemia peripheral arterial tonometry index ≤2.0, 21 patients (9.5%) were diagnosed with incident solid-tumor cancer during follow-up, whereas of 267 patients with a baseline reactive hyperemia peripheral arterial tonometry index >2.0, 10 patients (3.7%) were diagnosed with incident solid-tumor cancer during follow-up ( p = 0.009). Patients with a reactive hyperemia peripheral arterial tonometry index ≤2.0 had lower solid-tumor cancer-free survival compared to patients with a reactive hyperemia peripheral arterial tonometry index >2.0 (log-rank p = 0.017) (median follow-up 6.0 (3.0–9.1) years). Cox proportional hazard analyses showed that a reactive hyperemia peripheral arterial tonometry index ≤2.0 predicted the incidence of solid-tumor cancer, with a hazard ratio of 2.52 (95% confidence interval 1.17–5.45; p = 0.019) after adjusting for age, sex, and coronary artery disease, 2.83 (95% confidence interval 1.30–6.17; p = 0.009) after adjusting for diabetes mellitus, hypertension, smoking status, and body mass index >30 kg/m 2 , 2.79 (95% confidence interval 1.21–6.41; p = 0.016) after adjusting for fasting plasma glucose, systolic blood pressure, smoking status (current or former), and body mass index, and 2.43 (95% confidence interval 1.10–5.34; p = 0.028) after adjusting for Framingham risk score. Conclusion Microvascular endothelial dysfunction, as defined by a reactive hyperemia peripheral arterial tonometry index ≤2.0, was associated with a greater than two-fold increased risk of solid-tumor cancer. Microvascular endothelial dysfunction may be a useful marker to predict the future risk of solid-tumor cancer, in addition to its known ability to predict cardiovascular disease. Further research is necessary to develop adequate cancer screening strategies for patients with microvascular endothelial dysfunction.
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Toya et al. (2019) conducted a cohort in Patients undergoing microvascular endothelial function assessment (n=488). Microvascular endothelial dysfunction (reactive hyperemia peripheral arterial tonometry index ≤2.0) vs. Reactive hyperemia peripheral arterial tonometry index >2.0 was evaluated on Incident solid-tumor cancer (HR 2.52, 95% CI 1.17-5.45, p=0.019). Microvascular endothelial dysfunction (reactive hyperemia peripheral arterial tonometry index ≤2.0) predicted incident solid-tumor cancer (9.5% vs 3.7%; adjusted HR 2.52, 95% CI 1.17-5.45; p=0.019).
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