Circulating Vascular Cell Adhesion Molecule-1 and Incident Heart Failure: The Multi-Ethnic Study of Atherosclerosis
Ravi B Patel1,2, Laura A Colangelo2, Suzette J Bielinski3
1Division of Cardiology Department of Medicine Northwestern University Feinberg School of Medicine Chicago IL.
Insights
Serum levels of vascular cell adhesion molecule-1 (VCAM-1) indicate endothelial activation. Higher VCAM-1 levels are linked to increased risk of developing heart failure (HF), particularly HF with preserved ejection fraction (HFpEF).
Area of Science:
- Cardiovascular Disease Epidemiology
- Biomarkers of Endothelial Dysfunction
- Heart Failure Pathogenesis
Background:
- Serum vascular cell adhesion molecule-1 (VCAM-1) reflects endothelial activation.
- VCAM-1 is implicated in heart failure with preserved ejection fraction (HFpEF) pathogenesis.
- The prospective association of VCAM-1 with incident heart failure (HF) across ejection fraction categories is not well-established.
Purpose of the Study:
- To evaluate the association between VCAM-1 levels and the development of incident HF.
- To investigate if this association differs between HFpEF and HF with reduced ejection fraction (HFrEF).
- To explore the role of endothelial activation in HF development within a multiethnic cohort.
Main Methods:
- Utilized data from the Multi-Ethnic Study of Atherosclerosis (MESA) cohort.
- Assessed VCAM-1 levels at examination 2 (2002-2004) in 2297 participants.
- Tracked incident HF (HFpEF and HFrEF) adjudicated as first symptomatic HF hospitalization over a median of 14.4 years, adjusting for cardiovascular risk factors.
Main Results:
- Higher VCAM-1 levels were associated with being White, higher blood pressure, and lower kidney function.
- Each doubling of VCAM-1 was independently associated with a 94% increased risk of incident HF (HR, 1.94; P=0.01).
- VCAM-1 was significantly associated with incident HFpEF (HR, 1.97; P=0.04) but not significantly with HFrEF (HR, 1.82; P=0.16).
Conclusions:
- VCAM-1 is a significant predictor of incident HF in a multiethnic population over long-term follow-up.
- Findings suggest endothelial activation contributes to clinical HF, especially HFpEF.
- Therapies targeting endothelial activation may offer a strategy to prevent HF development from cardiovascular risk factors.
Abstract:
Background Serum levels of vascular cell adhesion molecule-1 (VCAM-1) are reflective of endothelial activation. Although VCAM-1 has been implicated in the pathogenesis of heart failure with preserved ejection fraction (HFpEF), the prospective association of VCAM-1 with development of clinically overt heart failure (HF) across ejection fraction categories is unclear. Methods and Results In MESA (the Multi-Ethnic Study of Atherosclerosis), we evaluated the association of VCAM-1 at examination 2 (2002-2004) with incident HF (HFpEF and HF with reduced ejection fraction) after adjustment for cardiovascular risk factors. Incident HF was independently adjudicated as first hospitalization for symptomatic HF. Among 2297 participants (mean age, 63 years; women, 53%), those with higher VCAM-1 were more likely to be White race, had higher blood pressure, and had lower kidney function. Over a median of 14.4 years, there were 102 HF events (HFpEF=65; HF with reduced ejection fraction=37). After covariate adjustment, each doubling of VCAM-1 was associated with incident HF (hazard ratio [HR], 1.94; 95% CI, 1.17-3.23; P=0.01). This association appeared stronger among current/former smokers compared with never smokers. On evaluation of HF subtypes, VCAM-1 was associated with incident HFpEF (HR, 1.97; 95% CI, 1.04-3.72; P=0.04) but not with incident HF with reduced ejection fraction, although risk estimates were consistent (HR, 1.82; 95% CI, 0.79-4.21; P=0.16). Conclusions In a multiethnic cohort, VCAM-1 was significantly associated with incident HF over long-term follow-up. These findings suggest a potential role for endothelial activation in driving clinical HF, and specifically HFpEF. Therapies that decrease endothelial activation may prevent the progression from cardiovascular risk factors to clinical HF.
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