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Vasoactive Biomarkers Associated With Long-Term Incidence of Symptomatic Peripheral Arterial Disease and Mortality
Ardwan Dakhel1,2, Gunnar Engström1, Olle Melander1,3
1Department of Clinical Sciences, Malmö, 5193Lund University, Sweden.
Insights
Plasma biomarkers like CT-proET-1, NT-proSST, and MR-proANP predict peripheral arterial disease (PAD) risk. All tested vasoactive biomarkers are associated with increased mortality risk in longitudinal studies.
Area of Science:
- Cardiovascular Medicine
- Biomarker Discovery
- Epidemiology
Background:
- Peripheral arterial disease (PAD) and mortality are significant health concerns.
- Early prediction of PAD and mortality is crucial for timely intervention.
- Plasma biomarkers offer a potential avenue for risk stratification.
Purpose of the Study:
- To evaluate the predictive value of specific plasma biomarkers for incident PAD and mortality.
- To assess the association of C-terminal endothelin-1 (CT-proET-1), N-Terminal prosomatostatin (NT-proSST), midregional proatrial natriuretic peptide (MR-proANP), procalcitonin (PCT), and copeptin with PAD and mortality.
Main Methods:
- Longitudinal cohort study including men and women from the Malmö Preventive Project.
- Analysis of five plasma biomarkers: CT-proET-1, NT-proSST, MR-proANP, PCT, and copeptin.
- Follow-up for incident PAD and mortality until December 31, 2016, using Cox proportional hazards regression models.
Main Results:
- Higher levels of CT-proET-1, NT-proSST, and MR-proANP were independently associated with incident PAD.
- All tested biomarkers (CT-proET-1, NT-proSST, MR-proANP, PCT, and copeptin) were independently associated with mortality.
- Cumulative incidence of PAD was 4.3% over a median follow-up of 11.2 years.
Conclusions:
- CT-proET-1, NT-proSST, and MR-proANP are valuable predictors of incident PAD.
- All evaluated vasoactive biomarkers serve as independent predictors of mortality.
- These biomarkers may aid in identifying individuals at higher risk for PAD and adverse cardiovascular outcomes.
Abstract:
We evaluated if plasma biomarkers can predict incident peripheral arterial disease (PAD) and mortality in a longitudinal cohort study. Men (n = 3618) and women (n = 1542) were included in the Malmö Preventive Project and underwent analysis of: C-terminal endothelin-1 (CT-proET-1), N-Terminal prosomatostatin (NT-proSST), midregional proatrial natriuretic peptide (MR-proANP), procalcitonin (PCT), and copeptin. Participants were followed up for incident PAD and mortality until December 31, 2016. Median follow-up was 11.2 years (interquartile range 9.4-12.2). Cumulative incidence of PAD was 4.3% (221/5160), 4.5% in men (164/3618) and 3.7% in women (57/1542; P = .174). In an adjusted Cox proportional hazards regression model, higher CT-proET-1 (hazard ratio [HR] 1.8; 95% confidence interval [CI] 1.4-2.3), NT-proSST (HR 1.5; 95% CI 1.2-2.0), and MR-proANP (HR 1.7; 95% CI 1.3-2.3) were independently associated with incident PAD, and higher CT-proET-1 (HR 1.3; 95% CI 1.2-1.5), NT-proSST (HR 1.2; 95% CI 1.1-1.3), MR-proANP (HR 1.4; 95% CI 1.3-1.6), PCT (HR 1.1; 95% CI 1.0-1.2), and copeptin (HR 1.2; 95% CI 1.1-1.4) were independently associated with mortality. Increased levels of CT-proET-1, NT-proSST, and MR-proANP were independently associated with incident PAD, whereas all the vasoactive biomarkers were independently associated with mortality during follow-up.
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