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.
Abstract

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