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Lipoprotein(a) and the Early Diagnosis, Complexity, and Extent of Coronary Artery Disease and Myocardial Infarction
Casper F Coerkamp1, Victor A Verpalen2, Kaoutar Bouhbouh1
1Department of Cardiology, Heart Center, Amsterdam University Medical Center, Amsterdam Cardiovascular Sciences, Amsterdam, the Netherlands.
Insights
Very high Lipoprotein(a) [Lp(a)] levels are linked to earlier diagnosis of obstructive coronary artery disease (CAD) and myocardial infarction (MI). Individuals with elevated Lp(a) face a significantly higher risk of recurrent MI.
Area of Science:
- Cardiology
- Lipid Metabolism
- Cardiovascular Risk Factors
Background:
- Lipoprotein(a) [Lp(a)] is a recognized, independent causal risk factor for coronary artery disease (CAD).
- Understanding the clinical implications of elevated Lp(a) is crucial for cardiovascular risk stratification.
Purpose of the Study:
- To investigate the association between very high Lp(a) levels and the diagnosis, clinical presentation, and angiographic features of obstructive CAD.
- To evaluate the impact of Lp(a) on the occurrence of myocardial infarction (MI), including ST-segment elevation MI and recurrent MI.
Main Methods:
- A case-control study involving 446 individuals with very high Lp(a) (>230 nmol/L) and 223 controls with low Lp(a) (≤7 nmol/L).
- Propensity score matching was used to balance groups by age and sex.
- Kaplan-Meier analysis assessed CAD- and MI-free survival; multivariable logistic regression analyzed associations with multivessel disease and SYNergy Between percutaneous coronary intervention with TAXus and Cardiac Surgery-1 (SYNTAX) score.
Main Results:
- Individuals with very high Lp(a) exhibited significantly lower event-free survival for obstructive CAD diagnosis and MI occurrence (P=0.006 and P=0.012, respectively).
- Elevated Lp(a) was associated with multivessel CAD (adjusted OR: 1.43 per 100 nmol/L; P=0.028).
- Very high Lp(a) carriers had a 2.4-fold higher risk of ST-segment elevation MI and a 15.9-fold higher risk of recurrent MI compared to controls.
Conclusions:
- Very high Lp(a) levels are associated with an earlier onset of obstructive CAD and MI, particularly ST-segment elevation MI.
- Individuals with very high Lp(a) demonstrate a substantially elevated risk for recurrent MI, underscoring the need for targeted management strategies.
Background:
Lipoprotein(a) [Lp(a)] is a potent, independent causal risk factor for coronary artery disease (CAD).
Objectives:
This study aimed to assess the association between Lp(a) and the diagnosis, clinical presentation, and angiographic characteristics of obstructive CAD and occurrence of myocardial infarction (MI).
Methods:
We included 446 individuals with very high Lp(a) (>230 nmol/L) who underwent routine lipid profiling, matched 2:1 by age and sex using nearest-neighbor propensity matching to 223 controls with low Lp(a) (≤7 nmol/L). Kaplan-Meier analysis was used to assess CAD- and MI-free survival. Multivariable ORs were calculated for multivessel disease and the SYNergy Between percutaneous coronary intervention with TAXus and Cardiac Surgery-1 score.
Results:
Median follow-up time, defined by age at last follow-up, was 60 years (Q1-Q3: 50-71). Individuals with very high Lp(a) had significantly lower event-free survival time for the diagnosis of obstructive CAD and occurrence of MI (P = 0.006 and P = 0.012, respectively). In multivariable analysis, Lp(a) was associated with multivessel CAD (adjusted OR: 1.43 [per 100 nmol/L]; 95% CI: 1.04-1.96; P = 0.028), but not with an intermediate or high SYNergy Between percutaneous coronary intervention with TAXus and Cardiac Surgery-1 score (adjusted OR: 1.28 [per 100 nmol/L]; 95% CI: 0.82-1.99, P = 0.279). Individuals with very high Lp(a) levels had a 2.4-fold higher risk of ST-segment elevation MI and a 15.9-fold higher risk of recurrent MI compared to those with low Lp(a).
Conclusions:
Very high Lp(a) is associated with earlier diagnosis of obstructive CAD and MI, predominantly ST-segment elevation MI. In addition, individuals with very high Lp(a) levels seem at a particular high risk of recurrent MI.
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