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The association of lipoprotein(a) with incident heart failure hospitalization: Atherosclerosis Risk in Communities
Anandita Agarwala1, Yashashwi Pokharel2, Anum Saeed3
1Department of Medicine, Baylor College of Medicine, Houston, TX, USA.
Insights
High lipoprotein(a) [Lp(a)] levels increase heart failure hospitalization risk. This association disappeared after excluding myocardial infarction cases, suggesting Lp(a) may not independently predict heart failure.
Area of Science:
- Cardiology
- Vascular Biology
- Epidemiology
Background:
- Lipoprotein(a) [Lp(a)] is a known risk factor for cardiovascular diseases like coronary heart disease and stroke.
- Emerging evidence links Lp(a) to aortic stenosis and heart failure (HF).
Purpose of the Study:
- To investigate the association between Lp(a) levels and incident HF hospitalization.
- To explore arterial stiffness as a potential mechanism linking Lp(a) to HF.
Main Methods:
- Analysis of 14,154 participants from the Atherosclerosis Risk in Communities (ARIC) study without prevalent HF.
- Utilized Cox proportional-hazards models to assess Lp(a) quintiles and incident HF hospitalization.
- Examined arterial stiffness parameters stratified by Lp(a) levels.
Main Results:
- A direct association was observed between higher Lp(a) levels and increased risk of HF hospitalization (HR 1.24, 95% CI 1.09-1.41).
- This association lost statistical significance after excluding participants with prevalent or incident myocardial infarction (HR 1.07, 95% CI 0.91-1.27).
- No significant association was found between Lp(a) levels and arterial stiffness parameters.
Conclusions:
- Elevated Lp(a) levels are associated with an increased risk of HF hospitalization.
- The observed association appears mediated by myocardial infarction, suggesting Lp(a) may not be an independent predictor of HF.
- Lp(a) is not significantly associated with arterial stiffness in this cohort.
Background And Aims:
Lipoprotein(a) [Lp(a)] is a proatherogenic lipoprotein associated with coronary heart disease, ischemic stroke, and more recently aortic stenosis and heart failure (HF). We examined the association of Lp(a) levels with incident HF hospitalization in the Atherosclerosis Risk in Communities (ARIC) study. We also assessed the relationship between Lp(a) levels and arterial stiffness as a potential mechanism for development of HF.
Methods:
Lp(a) was measured in 14,154 ARIC participants without prevalent HF at ARIC visit 1 (1987-1989). The association of Lp(a) quintiles with incident HF hospitalization was assessed using Cox proportional-hazards models. Arterial stiffness parameters were stratified based on Lp(a) quintiles, and p-trend was calculated across ordered groups.
Results:
At a median follow-up of 23.4 years, there were 2605 incident HF hospitalizations. Lp(a) levels were directly associated with incident HF hospitalization in models adjusted for age, race, gender, systolic blood pressure, history of hypertension, diabetes, smoking status, body mass index, heart rate, and high-density lipoprotein cholesterol (quintile 5 vs. quintile 1: hazard ratio [HR] 1.24, 95% confidence interval [CI] 1.09-1.41; p-trend across increasing quintiles <0.01), but not after excluding prevalent and incident myocardial infarction cases (HR 1.07, 95% CI 0.91-1.27; p-trend = 0.70). When adjusted for age, gender, and race, Lp(a) quintiles were not significantly associated with arterial stiffness parameters.
Conclusions:
Increased Lp(a) levels were associated with increased risk of incident HF hospitalization. After excluding prevalent and incident myocardial infarction, the association was no longer significant. Lp(a) levels were not associated with arterial stiffness parameters.
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