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Updated: May 3, 2026

High-Density Lipoprotein-Specific Phospholipid Efflux Assay
Published on: September 30, 2025
Lipoprotein(a) cascade screening in coronary artery disease
Karin Littmann1, Daniel Eriksson Hogling1, Mustafa Suhel1
1Department of Medicine Huddinge, Karolinska Institutet, Department of Endocrinology Karolinska University Hospital, Stockholm, Sweden.
Insights
Cascade screening for elevated lipoprotein(a) [Lp(a)] in coronary artery disease (CAD) patients’ relatives is feasible. This approach is significantly more effective when initiated from individuals with high Lp(a) levels.
Area of Science:
- Cardiovascular Medicine
- Genetics
- Public Health Screening
Background:
- Elevated lipoprotein(a) [Lp(a)] is a significant risk factor for coronary artery disease (CAD).
- Cascade screening offers a potential strategy to identify individuals at genetic risk for CAD.
- Understanding the effectiveness of Lp(a)-based cascade screening is crucial for clinical implementation.
Purpose of the Study:
- To evaluate the effectiveness of cascade screening for elevated Lp(a) in relatives of patients with CAD.
- To determine the yield of identifying elevated Lp(a) in first-degree relatives (FDR) and second-degree relatives (SDR) based on the index patient's Lp(a) level.
Main Methods:
- Cascade screening was performed in FDR and SDR of index patients with CAD.
- Index patients were stratified into low, moderately elevated, and elevated Lp(a) groups.
- The proportion of relatives with elevated Lp(a) and participation rates were analyzed within each stratum.
Main Results:
- Out of 1120 invited relatives, 764 (68.2%) were screened.
- Elevated Lp(a) was found in 30.2% of FDR and 19.4% of SDR from index patients with elevated Lp(a), versus 6.2% and 5.6% from those with low Lp(a), respectively.
- Screening was more efficient when initiated from index patients with elevated Lp(a), requiring fewer relatives to be screened to identify one affected individual.
Conclusions:
- Cascade screening for elevated Lp(a) is a feasible strategy in a real-world setting for relatives of CAD patients.
- The effectiveness of cascade screening is significantly higher when the index patient has elevated Lp(a).
- This approach can efficiently identify at-risk relatives for further cardiovascular risk management.
Background And Aim:
Elevated lipoprotein(a) [Lp(a)] contributes to coronary artery disease (CAD). This study aimed to determine the effectiveness of cascade screening for elevated Lp(a) in patients with CAD.
Methods:
Lp(a)-based cascade screening in first-degree relatives (FDR) and second-degree relatives (SDR) of index patients with CAD was performed. Index patients were recruited into pre-defined Lp(a) strata: low (<70 nmol/L), moderately elevated (70-169 nmol/L), and elevated (≥170 nmol/L). Proportions of elevated Lp(a) in relatives were determined within each index stratum, and participation rate was evaluated.
Results:
735 index patients (mean age 66.5 years, 76.9% male) participated, with 333, 149, and 253 in the low, moderately elevated, and elevated Lp(a) strata, respectively. Of 1120 invited relatives, 764 relatives (68.2%) were screened. Lp(a) was elevated in 30.2% of FDR and 19.4% of SDR of index patients with elevated Lp(a) compared with 6.2% in FDR (p < 0.001) and 5.6% in SDR (p = 0.007) of index patients with low Lp(a). The number (95%CI) of FDR needed to be screened to identify one individual with elevated Lp(a) was 3.3 (2.7-4.2) when the index patient had elevated Lp(a), compared with 16.1 (10.0-30.8) for low Lp(a) (p < 0.001). Corresponding numbers for SDR were 5.1 (3.4-8.8) and 17.8 (9.3-45.2) (p = 0.006).
Conclusions:
Cascade screening for elevated Lp(a) in relatives of patients with CAD is feasible in a real-world setting. Screening was up to five times more effective when initiated from patients with elevated Lp(a) than with low.
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