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A High-Throughput NMR Method for Lipoprotein-X Quantification.

Erwin GarciaIrina ShalaurovaSteven P MatyusLita A FreemanEdward B NeufeldMaureen L SampsonRafael ZubiránAnna WolskaAlan T RemaleyJames D OtvosMargery A Connelly
Published in: Molecules (Basel, Switzerland) (2024)
Lipoprotein X (LP-X) is an abnormal cholesterol-rich lipoprotein particle that accumulates in patients with cholestatic liver disease and familial lecithin-cholesterol acyltransferase deficiency (FLD). Because there are no high-throughput diagnostic tests for its detection, a proton nuclear magnetic resonance (NMR) spectroscopy-based method was developed for use on a clinical NMR analyzer commonly used for the quantification of lipoproteins and other cardiovascular biomarkers. The LP-X assay was linear from 89 to 1615 mg/dL (cholesterol units) and had a functional sensitivity of 44 mg/dL. The intra-assay coefficient of variation (CV) varied between 1.8 and 11.8%, depending on the value of LP-X, whereas the inter-assay CV varied between 1.5 and 15.4%. The assay showed no interference with bilirubin levels up to 317 mg/dL and was also unaffected by hemolysis for hemoglobin values up to 216 mg/dL. Samples were stable when stored for up to 6 days at 4 °C but were not stable when frozen. In a large general population cohort ( n = 277,000), LP-X was detected in only 50 subjects. The majority of LP-X positive cases had liver disease (64%), and in seven cases, had genetic FLD (14%). In summary, we describe a new NMR-based assay for LP-X, which can be readily implemented for routine clinical laboratory testing.
Keyphrases
  • high throughput
  • magnetic resonance
  • low density lipoprotein
  • single cell
  • magnetic resonance imaging
  • genome wide
  • computed tomography
  • mass spectrometry
  • dna methylation
  • liver injury