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Published on: October 12, 2017
Impact of elevated lipoprotein(a) on coronary artery disease phenotype and severity
David M Leistner1,2,3,4,5, Andres Laguna-Fernandez6, Arash Haghikia1,2,3,4
1Department of Cardiology, Campus Benjamin Franklin (CBF), Charité-Universitätsmedizin Berlin, Hindenburgdamm 30, 12203 Berlin, Germany.
Insights
Elevated lipoprotein(a) [Lp(a)] is linked to more severe coronary artery disease (CAD). Monitoring Lp(a) levels can inform clinical management strategies for patients with CAD.
Area of Science:
- Cardiology
- Lipidology
- Atherosclerosis Research
Background:
- A clear understanding of the link between elevated lipoprotein(a) [Lp(a)] and coronary artery disease (CAD) severity is needed.
- Lipoprotein(a) is an independent risk factor for atherosclerotic cardiovascular disease.
Purpose of the Study:
- To quantitatively assess the association between increasing lipoprotein(a) levels and coronary artery disease severity.
- To evaluate Lp(a) levels in a real-world patient population undergoing angiography.
Main Methods:
- A non-interventional, cross-sectional study (LipidCardio) included 975 patients aged ≥21 years undergoing coronary angiography.
- Lipoprotein(a) levels were measured, and coronary artery disease severity was assessed using SYNTAX-I and Gensini scores.
- Patients were stratified based on baseline Lp(a) levels.
Main Results:
- Higher Lp(a) levels (≥150 nmol/L) were associated with a greater prevalence of prior CAD, prior coronary revascularization, and complex coronary lesions.
- Patients with elevated Lp(a) exhibited significantly higher median SYNTAX-I and Gensini scores compared to those with normal Lp(a) levels.
- A higher proportion of patients with elevated Lp(a) had diffusely narrowed vessels or chronic total occlusions.
Conclusions:
- Elevated lipoprotein(a) levels are significantly associated with a more severe presentation of coronary artery disease.
- Measuring Lp(a) levels in patients with CAD may offer valuable insights for clinical decision-making and risk stratification.
Aims:
A thorough characterization of the relationship between elevated lipoprotein(a) [Lp(a)] and coronary artery disease (CAD) is lacking. This study aimed to quantitatively assess the association of increasing Lp(a) levels and CAD severity in a real-world population.
Methods And Results:
This non-interventional, cross-sectional, LipidCardio study included patients aged ≥21 years undergoing angiography (October 2016-March 2018) at a tertiary cardiology centre, who have at least one Lp(a) measurement. The association between Lp(a) and CAD severity was determined by synergy between PCI with taxus and cardiac surgery (SYNTAX)-I and Gensini scores and angiographic characteristics. Overall, 975 patients (mean age: 69.5 years) were included; 70.1% were male, 97.5% had Caucasian ancestry, and 33.2% had a family history of premature atherosclerotic cardiovascular disease. Median baseline Lp(a) level was 19.3 nmol/L. Patients were stratified by baseline Lp(a): 72.9% had < 65 nmol/L, 21.0% had ≥100 nmol/L, 17.2% had ≥125 nmol/L, and 12.9% had ≥150 nmol/L. Compared with the normal (Lp(a) < 65 nmol/L) group, elevated Lp(a) groups (e.g. ≥ 150 nmol/L) had a higher proportion of patients with prior CAD (48.4% vs. 62.7%; P < 0.01), prior coronary revascularization (39.1% vs. 51.6%; P = 0.01), prior coronary artery bypass graft (6.0% vs. 15.1%; P < 0.01), vessel(s) with lesions (68.5% vs. 81.3%; P = 0.03), diffusely narrowed vessels (10.9% vs. 16.5%; P = 0.01) or chronic total occlusion lesions (14.3% vs. 25.2%; P < 0.01), and higher median SYNTAX-I (3.0 vs. 5.5; P = 0.01) and Gensini (10.0 vs. 16.0; P < 0.01) scores.
Conclusion:
Elevated Lp(a) was associated with a more severe presentation of CAD. Awareness of Lp(a) levels in patients with CAD may have implications in their clinical management.
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