Identifying Familial Hypercholesterolemia Using a Blood Donor Screening Program With More Than 1 Million Volunteer

Candace L Jackson1,2, James Z Keeton1, Stephen J Eason3

  • 1University of Texas Southwestern Medical Center, Dallas.

JAMA Cardiology
|May 23, 2019
PubMed

Insights

Familial hypercholesterolemia (FH) affects 1 in 339 blood donors, similar to the general population. Blood donor screening offers a novel strategy for early FH detection and cascade screening, especially in younger individuals.

Area of Science:

  • Cardiovascular Medicine
  • Genetics
  • Public Health

Background:

  • Familial hypercholesterolemia (FH) is an autosomal-dominant disorder leading to premature coronary artery disease.
  • FH is often undiagnosed, despite its significant health implications.

Purpose of the Study:

  • To estimate the prevalence of familial hypercholesterolemia (FH) within a large blood donor population.
  • To explore the potential of blood donor screening as a method for identifying individuals with FH.

Main Methods:

  • Analysis of deidentified data from over 1 million blood donors (2002-2016).
  • Utilized the Make Early Diagnosis to Prevent Early Death (MEDPED) criteria for FH diagnosis based on total nonfasting serum cholesterol levels.
  • Established age-specific cholesterol thresholds for FH identification.

Main Results:

  • Identified 3,473 individuals (1 in 339) meeting FH criteria.
  • Prevalence was higher in younger donors (<30 years: 1:257) and men (1:327).
  • Median total cholesterol in identified FH individuals was 332 mg/dL.

Conclusions:

  • The prevalence of FH in blood donors mirrors that of the general population.
  • Blood donor screening presents a viable, novel strategy for detecting FH, particularly in younger populations.
  • This approach can facilitate early intervention and guide cascade screening efforts for FH.
Abstract

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