Measuring the contribution of Lp(a) cholesterol towards LDL-C interpretation

Clin Biochem. 2020 Dec:86:45-51. doi: 10.1016/j.clinbiochem.2020.09.007. Epub 2020 Sep 28.

Abstract

Background: Lipoprotein(a) [Lp(a)] is a pro-atherogenic and pro-thrombotic LDL-like particle recognized as an independent risk factor for cardiovascular disease (CVD). The cholesterol within Lp(a) (Lp(a)-C) contributes to the reported LDL-cholesterol (LDL-C) concentration by nearly all available methods. Accurate LDL-C measurements are critical for identification of genetic dyslipidemias such as familial hypercholesterolemia (FH). FH diagnostic criteria, such as the Dutch Lipid Clinic Network (DLCN) criteria, utilize LDL-C concentration cut-offs to assess the likelihood of FH. Therefore, failure to adjust for Lp(a)-C can impact accurate FH diagnosis and classification, appropriate follow-up testing and treatments, and interpretation of cholesterol-lowering treatment efficacy.

Objective: In this study, we use direct Lp(a)-C measurements to assess the potential misclassification of FH from contributions of Lp(a)-C to reported LDL-C in patient samples submitted for advanced lipoprotein profiling.

Methods: A total of 31,215 samples submitted for lipoprotein profiling were included. LDL-C was measured by beta quantification or calculated by one of three equations. Lp(a)-C was measured by quantitative lipoprotein electrophoresis. DLCN LDL-C cut-offs were applied to LDL-C results before and after accounting for Lp(a)-C contribution.

Results: Lp(a)-C was detected in 8665 (28%) samples. A total of 940 subjects were reclassified to a lower DLCN LDL-C categories; this represents 3% of the total patient series or 11% of subjects with measurable Lp(a)-C.

Conclusion: Lp(a)-C is present in a significant portion of samples submitted for advanced lipid testing and could cause patient misclassification when using FH diagnostic criteria. These misclassifications could trigger inappropriate follow-up, treatment, and cascade testing for suspected FH.

Keywords: Familial hypercholesterolemia; Lipid phenotyping; Lipoprotein(a); Low-density lipoprotein cholesterol; Risk classification.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Cholesterol, LDL / blood*
  • Databases, Factual
  • False Positive Reactions
  • Female
  • Humans
  • Hyperlipoproteinemia Type II / blood*
  • Hyperlipoproteinemia Type II / diagnosis*
  • Lipoprotein(a) / blood*
  • Lipoprotein(a) / chemistry*
  • Male
  • Middle Aged
  • Young Adult

Substances

  • Cholesterol, LDL
  • Lipoprotein(a)