Abstract

Serum concentrations of lathosterol, the plant sterols campesterol and sitosterol and the cholesterol metabolite 5α-cholestanol are widely used as surrogate markers of cholesterol synthesis and absorption, respectively. Increasing numbers of laboratories utilize a broad spectrum of well-established and recently developed methods for the determination of cholesterol and non-cholesterol sterols (NCS). In order to evaluate the quality of these measurements and to identify possible sources of analytical errors our group initiated the first international survey for cholesterol and NCS. The cholesterol and NCS survey was structured as a two-part survey which took place in the years 2013 and 2014. The first survey part was designed as descriptive, providing information about the variation of reported results from different laboratories. A set of two lyophilized pooled sera (A and B) was sent to twenty laboratories specialized in chromatographic lipid analysis. The different sterols were quantified either by gas chromatography-flame ionization detection, gas chromatography- or liquid chromatography-mass selective detection. The participants were requested to determine cholesterol and NCS concentrations in the provided samples as part of their normal laboratory routine. The second part was designed as interventional survey. Twenty-two laboratories agreed to participate and received again two different lyophilized pooled sera (C and D). In contrast to the first international survey, each participant received standard stock solutions with defined concentrations of cholesterol and NCS. The participants were requested to use diluted calibration solutions from the provided standard stock solutions for quantification of cholesterol and NCS. In both surveys, each laboratory used its own internal standard (5α-cholestane, epicoprostanol or deuterium labelled sterols).Main outcome of the survey was, that unacceptably high interlaboratory variations for cholesterol and NCS concentrations are reported, even when the individual laboratories used the same calibration material. We discuss different sources of errors and recommend all laboratories analysing cholesterol and NCS to participate in regular quality control programs.

Highlights

  • Serum or plasma concentrations of the cholesterol precursors lanosterol, lathosterol, and desmosterol are widely used as surrogate markers of endogenous cholesterol synthesis [1]

  • These non-cholesterol sterols (NCS) show even stronger correlations with cholesterol absorption and synthesis when expressed as ratios to total cholesterol, which standardizes for variations in sterol transport protein concentrations [4]

  • The first part of the cholesterol and NCS survey was initiated in the year 2013 under the expertise of the German Reference Institute for Bioanalytics (RfB) and the Laboratory for Specialized Lipid Diagnostic of the University Hospital, both located in Bonn, Germany

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Summary

Introduction

Serum or plasma concentrations of the cholesterol precursors lanosterol, lathosterol, and desmosterol are widely used as surrogate markers of endogenous cholesterol synthesis [1]. The cholesterol metabolite 5α-cholestanol and the plant sterols campesterol and sitosterol are used as markers of cholesterol absorption [2,3] These non-cholesterol sterols (NCS) show even stronger correlations with cholesterol absorption and synthesis when expressed as ratios to total cholesterol, which standardizes for variations in sterol transport protein concentrations [4]. The interest in surrogate markers of cholesterol metabolism is recently increasing and more laboratories develop new methods for the determination of cholesterol and NCS using different chromatographic separation and mass spectrometric detection methods. We reflect the comparability of cholesterol and NCS concentrations determined by different separation and detection methods and discuss the suitability of different compounds used as internal standards for sterol quantification. The focus was on the influence of the utilized calibration solutions and the participants were requested to use provided stock solutions for the quantification of the sample material

Materials and methods
The first international cholesterol and NCS survey
The second international cholesterol and NCS survey
Statistical analysis
Participants total cholesterol
Participants
Cholesterol
Lathosterol
Campesterol
Sitosterol
Common discussion
Conclusions
Full Text
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