Single Nucleotide Variants Associated With Polygenic Hypercholesterolemia in Families Diagnosed Clinically With Familial Hypercholesterolemia

Rev Esp Cardiol (Engl Ed). 2018 May;71(5):351-356. doi: 10.1016/j.rec.2017.07.010. Epub 2017 Sep 14.
[Article in English, Spanish]

Abstract

Introduction and objectives: Approximately 20% to 40% of clinically defined familial hypercholesterolemia cases do not show a causative mutation in candidate genes, and some of them may have a polygenic origin. A cholesterol gene risk score for the diagnosis of polygenic hypercholesterolemia has been demonstrated to be valuable to differentiate polygenic and monogenic hypercholesterolemia. The aim of this study was to determine the contribution to low-density lipoprotein cholesterol (LDL-C) of the single nucleotide variants associated with polygenic hypercholesterolemia in probands with genetic hypercholesterolemia without mutations in candidate genes (nonfamilial hypercholesterolemia genetic hypercholesterolemia) and the genetic score in cascade screening in their family members.

Methods: We recruited 49 nonfamilial hypercholesterolemia genetic hypercholesterolemia families (294 participants) and calculated cholesterol gene scores, derived from single nucleotide variants in SORT1, APOB, ABCG8, APOE and LDLR and lipoprotein(a) plasma concentration.

Results: Risk alleles in SORT1, ABCG8, APOE, and LDLR showed a statistically significantly higher frequency in blood relatives than in the 1000 Genomes Project. However, there were no differences between affected and nonaffected members. The contribution of the cholesterol gene score to LDL-C was significantly higher in affected than in nonaffected participants (P = .048). The percentage of the LDL-C variation explained by the score was 3.1%, and this percentage increased to 6.9% in those families with the highest genetic score in the proband.

Conclusions: Nonfamilial hypercholesterolemia genetic hypercholesterolemia families concentrate risk alleles for high LDL-C. Their contribution varies greatly among families, indicating the complexity and heterogeneity of these forms of hypercholesterolemias. The gene score explains a small percentage of LDL-C, which limits its use in diagnosis.

Keywords: Familial hypercholesterolemia; Hipercolesterolemia familiar; Hipercolesterolemia poligénica; Polygenic hypercholesterolemia; Single nucleotide variants; Variante de un solo nucleótido.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Aged
  • Alleles
  • Cholesterol, LDL / blood*
  • Cohort Studies
  • Female
  • Genetic Predisposition to Disease / epidemiology*
  • Humans
  • Hypercholesterolemia / blood
  • Hypercholesterolemia / diagnosis
  • Hypercholesterolemia / epidemiology
  • Hyperlipoproteinemia Type II / diagnosis
  • Hyperlipoproteinemia Type II / epidemiology
  • Hyperlipoproteinemia Type II / genetics*
  • Incidence
  • Male
  • Middle Aged
  • Mutation
  • Pedigree
  • Polymorphism, Single Nucleotide*
  • Prognosis
  • Proprotein Convertase 9 / genetics*
  • Retrospective Studies

Substances

  • Cholesterol, LDL
  • Proprotein Convertase 9