Characterization of familial hypercholesterolemia in Taiwanese ischemic stroke patients

Aging (Albany NY). 2021 Jul 27;13(15):19339-19351. doi: 10.18632/aging.203320. Epub 2021 Jul 27.

Abstract

Familial hypercholesterolemia (FH) is a common genetic disorder characterized by a lifelong elevated low-density lipoprotein cholesterol (LDL-C) level. The relationship between FH and ischemic stroke is still controversial. We enrolled ischemic stroke patients prospectively in our neurological ward, and divided them into two groups according to LDL-C levels with a threshold of 130 mg/dl. Targeted sequencing was performed in all stroke patients for LDLR, APOB, and PCSK9 genes. The fifty-eight high-LDL subjects were older, prevalence of previous myocardial infarction/stroke history was lower, and the first stroke age was older compared with values in the sixty-three low-LDL cases. The prevalence of FH in Han-Chinese stroke patients was 5.0%, and was 10.3% in those with a higher LDL-C level. We identified six carriers, who had higher percentages of large vessel stroke subtype (66.7% vs. 15.4%) and transient ischemic attack (33.3% vs. 3.8%), previous myocardial infarction/stroke history (50.0% vs. 11.5%), statin use (50.0% vs. 11.5%), and increased carotid intima-media thickness (IMT) (0.9-1.2mm vs.0.7-9.0mm) compared with the other hypercholesterolemic patients without pathogenic variants. Ischemic stroke patients carrying FH pathogenic variants seemed to have a higher risk for large artery stroke and transient ischemic attack. The IMT exam could be useful to screen for FH in hypercholesterolemic stroke patients.

Keywords: atherosclerosis; carotid intima-media thickness; familial hypercholesterolemia; ischemic stroke; low-density lipoprotein cholesterol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Apolipoprotein B-100 / genetics
  • Carotid Intima-Media Thickness
  • Cholesterol, LDL / blood*
  • Female
  • Heterozygote
  • Humans
  • Hyperlipoproteinemia Type II / blood*
  • Hyperlipoproteinemia Type II / diagnosis
  • Hyperlipoproteinemia Type II / epidemiology
  • Hyperlipoproteinemia Type II / genetics*
  • Ischemic Stroke / complications*
  • Male
  • Middle Aged
  • Mutation
  • Phenotype
  • Proprotein Convertase 9 / genetics
  • Receptors, LDL / genetics
  • Risk Factors
  • Taiwan / epidemiology

Substances

  • APOB protein, human
  • Apolipoprotein B-100
  • Cholesterol, LDL
  • LDLR protein, human
  • Receptors, LDL
  • PCSK9 protein, human
  • Proprotein Convertase 9