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Isolation and Analysis of Plasma Lipoproteins by Ultracentrifugation
Published on: January 28, 2021
Identification and characterization of severe familial hypercholesterolemia in patients presenting for cardiac
Barak Zafrir1, Chen Shapira2, Gil Lavie3
1Department of Cardiology, Lady Davis Carmel Medical Center, Haifa, Israel; Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
Insights
Identifying severe familial hypercholesterolemia (FH) is crucial. Screening cardiac catheterization databases found FH patients with high LDL-C, often undiagnosed and undertreated, highlighting the need for proactive management.
Area of Science:
- Cardiology
- Genetics
- Metabolic Disorders
Background:
- Severe familial hypercholesterolemia (FH) patients are frequently undiagnosed.
- Emerging PCSK9 inhibitors necessitate better identification of severe FH.
- Early identification is key for effective FH management.
Purpose of the Study:
- To identify, characterize, and manage severe FH patients.
- To screen cardiac catheterization (CC) databases for severe FH.
- To evaluate lipid levels and treatment in severe FH.
Main Methods:
- Retrospective analysis of CC database (2002-2015) for LDL-C ≥130 mg/dL.
- Severe FH diagnosis: prior LDL-C ≥280 mg/dL, excluding secondary causes.
- Screening for relatives using identifying data and age-dependent LDL-C cutoffs.
Main Results:
- 54 severe FH patients identified from 2382 CC patients.
- Mean age at cardiovascular disease diagnosis: 45 years; peak LDL-C median: 322 mg/dL.
- 161 additional possible FH individuals identified; 58% untreated.
Conclusions:
- A screening algorithm identified severe FH patients with early coronary disease.
- Many severe FH patients have suboptimal cholesterol treatment.
- Screening cardiovascular databases aids FH identification and family management.
Background:
Patients with severe familial hypercholesterolemia (FH) are often unrecognized despite typical presentation. The introduction of PCSK9 inhibitors opens new therapeutic options and emphasizes the need for identification of severe FH patients.
Objectives:
The objective was identification, characterization, and management of severe FH patients by screening of cardiac catheterization (CC) database.
Methods:
Retrospective analysis of CC database from 2002 to mid-2015 was performed for low-density lipoprotein cholesterol (LDL-C) ≥130 mg/dL (n = 2383). Severe FH was diagnosed if any prior LDL-C was ≥280 mg/dL, excluding secondary causes. Peak/current LDL-C levels and lipid-lowering therapies were evaluated. Initial attempt was made to detect relatives with FH according to identifying data and age-dependent LDL-C cutoffs.
Results:
Severe FH was identified in 54 of initial 2382 patients with CC LDL-C ≥130 mg/dL. Mean age at cardiovascular disease diagnosis was 45 years. Peak LDL-C was 280 to 464 mg/dL (median, 322). Coronary artery bypass graft surgery was performed in 26 patients (48%) and redo coronary artery bypass graft surgery in 5 patients (9%). Risk factors included obesity (33%), hypertension (59%), smoking (33%), and diabetes (24%). LDL-C reduction ≥50% of peak value was achieved in 56%, LDL-C <130 mg/dL in 32%, and LDL-C <100 mg/dL in 17% of patients. High-intensity statin plus ezetimibe was prescribed for 67%, high-intensity statin alone for 24%, and other lipid-lowering therapies for 9% of patients. Treatment intensity was directly associated with attainment of LDL-C goals. Matching probands' surnames and place of residency with district health maintenance organization database has identified 161 additional individuals with possible FH; 58% were not treated with lipid-lowering drugs.
Conclusions:
A simple algorithm for identification of patients with severe FH was implemented based on large catheterization and health maintenance organization databases and revealed patients with severe FH and coronary disease at a young age, with low attainment of cholesterol treatment goals. Screening existing cardiovascular databases of populations at risk will promote identification and management of severe FH patients and their affected family members.
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