Analysis of sterols by high-performance liquid chromatography/mass spectrometry combined with chemometrics

被引:25
作者
Kornel Nagy
Jakab, Annamaria
Ferenc Pollreisz
Bongiorno, David
Ceraulo, Leopoldo
Averna, Maurizio R.
Noto, Davide
Karoly Vekey
机构
[1] Hungarian Acad Sci, Chem Res Ctr, Dept Mass Spectrometry, Inst Struct Chem, H-1025 Budapest, Hungary
[2] Univ Palermo, Dept Chem & Pharmaceut Technol, I-90123 Palermo, Italy
[3] Univ Palermo, Dept Clin Med & Emerging Dis, I-90145 Palermo, Italy
关键词
D O I
10.1002/rcm.2606
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A newly developed high-performance liquid chromatography/mass spectrometry (HPLC/MS) method has been successfully used to analyze plasma concentrations of various phytosterols (cholestanol and beta-sitosterol) and cholesterol metabolites (desmosterol and lathosterol). This was based on an unusual solvent combination of water/methanol vs. methanol/acetone/n-hexane applied on a Purospher Star RP-18e (125 x 2 mm, 3 mu m) column, which proved excellent for the separation, identification and quantification of plasma sterols. Simple solid-phase extraction preparation of plasma samples was performed, followed by the developed fast and robust HPLC separation. Results on four groups of people were compared, those with low, normal and high plasma cholesterol levels and those with high cholesterol levels on statin therapy, and the results were evaluated using linear discriminant analysis (LDA). Variable selection for LDA was achieved using backward removal selection. Highly discriminatory variables were the ratios of desmosterol to sitosterol and of lathosterol to total plasma cholesterol. The latter ratio was also excellent for distinguishing subjects on statin therapy. The success rate of classification was 100%. The present pilot study shows the potential of HPLC/MS analysis and chemometrics for studying cholesterol-related disorders and warrants future full-scale medical study. Copyright (c) 2006 John Wiley & Sons, Ltd.
引用
收藏
页码:2433 / 2440
页数:8
相关论文
共 27 条
[1]   Comparative study of cardiovascular markers data by various techniques of multivariate analysis [J].
Balla, B ;
Mocak, J ;
Pivovarnikova, H ;
Balla, J .
CHEMOMETRICS AND INTELLIGENT LABORATORY SYSTEMS, 2004, 72 (02) :259-267
[2]   Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters [J].
Berge, KE ;
Tian, H ;
Graf, GA ;
Yu, LQ ;
Grishin, NV ;
Schultz, J ;
Kwiterovich, P ;
Shan, B ;
Barnes, R ;
Hobbs, HH .
SCIENCE, 2000, 290 (5497) :1771-1775
[3]   Oxysterols and atherosclerosis [J].
Brown, AJ ;
Jessup, W .
ATHEROSCLEROSIS, 1999, 142 (01) :1-28
[4]   Determination of 24S-and 27-hydroxycholesterol in plasma by high-performance liquid chromatography-mass spectrometry [J].
Burkard, I ;
Rentsch, KM ;
von Eckardstein, A .
JOURNAL OF LIPID RESEARCH, 2004, 45 (04) :776-781
[5]  
Byrdwell W. C., 2003, ADV LIPID METHODOLOG, P171
[6]   The bottom-up solution to the triacylglycerol lipidome using atmospheric pressure chemical ionization mass spectrometry [J].
Byrdwell, WC .
LIPIDS, 2005, 40 (04) :383-417
[7]   Atmospheric pressure chemical ionization mass spectrometry for analysis of lipids [J].
Byrdwell, WC .
LIPIDS, 2001, 36 (04) :327-346
[8]   The use and misuse of chemometrics for treating classification problems [J].
Defernez, M ;
Kemsley, EK .
TRAC-TRENDS IN ANALYTICAL CHEMISTRY, 1997, 16 (04) :216-221
[9]   Comparison of the intestinal uptake of cholesterol, plant sterols, and stanols in mice [J].
Igel, M ;
Giesa, U ;
Lütjohann, D ;
von Bergmann, K .
JOURNAL OF LIPID RESEARCH, 2003, 44 (03) :533-538
[10]  
Johnson DW, 2001, J LIPID RES, V42, P1699