Current status of familial hypercholesterolemia in Chinese populations

Curr Opin Lipidol. 2019 Apr;30(2):94-100. doi: 10.1097/MOL.0000000000000580.

Abstract

Purpose of review: Heterozygous familial hypercholesterolemia often went unrecognized in China when population cholesterol levels were low, but rapid economic development has changed the situation. This review will discuss the current position of awareness, diagnosis, and management of familial hypercholesterolemia in Chinese populations.

Recent findings: The phenotype of familial hypercholesterolemia in China and other Chinese populations has become similar to that in Western countries, although it may still be somewhat less severe. The prevalence in Chinese populations is also similar to that in other countries and it has been found in up to 7% of Chinese patients with premature coronary heart disease. Most of the mutations are in the low-density lipoprotein receptor gene but the pattern of mutations differs from that in Whites. Chinese patients may be more responsive to statins than Whites but patients with familial hypercholesterolemia are often undertreated.

Summary: Increasing population cholesterol levels have changed the phenotype of familial hypercholesterolemia in China and Chinese patients now resemble those in Western countries. International initiatives are facilitating increased awareness and identification of cases and more effective management of the condition.

Publication types

  • Review

MeSH terms

  • Anticholesteremic Agents / therapeutic use*
  • Apolipoprotein B-100 / genetics*
  • China / epidemiology
  • Cholesterol, LDL / blood
  • Coronary Disease / diagnosis
  • Coronary Disease / drug therapy
  • Coronary Disease / epidemiology*
  • Coronary Disease / genetics
  • Disease Management
  • Gene Expression
  • Genotype
  • Heterozygote
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors / therapeutic use*
  • Hyperlipoproteinemia Type II / diagnosis
  • Hyperlipoproteinemia Type II / drug therapy
  • Hyperlipoproteinemia Type II / epidemiology*
  • Hyperlipoproteinemia Type II / genetics
  • Mutation*
  • Prevalence
  • Receptors, LDL / genetics*
  • Severity of Illness Index

Substances

  • APOB protein, human
  • Anticholesteremic Agents
  • Apolipoprotein B-100
  • Cholesterol, LDL
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • LDLR protein, human
  • Receptors, LDL