Reliable determination of new lipid peroxidation compounds as potential early Alzheimer Disease biomarkers

Talanta. 2018 Jul 1:184:193-201. doi: 10.1016/j.talanta.2018.03.002. Epub 2018 Mar 6.

Abstract

Lipid peroxidation plays an important role in Alzheimer Disease, so corresponding metabolites found in urine samples could be potential biomarkers. The aim of this work is to develop a reliable ultra-performance liquid chromatography-tandem mass spectrometry analytical method to determine a new set of lipid peroxidation compounds in urine samples. Excellent sensitivity was achieved with limits of detection between 0.08 and 17 nmol L-1, which renders this method suitable to monitor analytes concentrations in real samples. The method's precision was satisfactory with coefficients of variation around 5-17% (intra-day) and 8-19% (inter-day). The accuracy of the method was assessed by analysis of spiked urine samples obtaining recoveries between 70% and 120% for most of the analytes. The utility of the described method was tested by analyzing urine samples from patients early diagnosed with mild cognitive impairment or mild dementia Alzheimer Disease following the clinical standard criteria. As preliminary results, some analytes (17(RS)-10-epi-SC-Δ15-11-dihomo-IsoF, PGE2) and total parameters (Neuroprostanes, Isoprostanes, Isofurans) show differences between the control and the clinical groups. So, these analytes could be potential early Alzheimer Disease biomarkers assessing the patients' pro-oxidant condition.

Keywords: Biomarker; Isofuran; Isoprostane; Lipid peroxidation; Mass spectrometry; Neurological damage; Urine.

MeSH terms

  • Alzheimer Disease / diagnosis
  • Alzheimer Disease / urine*
  • Biomarkers / urine
  • Chromatography, High Pressure Liquid
  • Furans / urine*
  • Humans
  • Isoprostanes / urine*
  • Lipid Peroxidation
  • Neuroprostanes / urine*
  • Receptors, Prostaglandin E, EP2 Subtype / analysis*
  • Tandem Mass Spectrometry

Substances

  • Biomarkers
  • Furans
  • Isoprostanes
  • Neuroprostanes
  • Receptors, Prostaglandin E, EP2 Subtype