Biological variation of β-sitosterol, campesterol, and lathosterol as cholesterol absorption and synthesis biomarkers

被引:18
|
作者
Wu, Alan H. B. [1 ]
Ruan, Weiming [1 ]
Todd, John [2 ]
Lynch, Kara L. [1 ]
机构
[1] Univ Calif San Francisco, San Francisco Gen Hosp, Dept Lab Med, Clin Chem Lab, San Francisco, CA 94143 USA
[2] Singluex Inc, Alameda, CA USA
关键词
beta-Sitosterol; Campesterol; Lathosterol; Biological variation; STATIN THERAPY; EZETIMIBE; EFFICACY; MARKERS; SAFETY;
D O I
10.1016/j.cca.2013.12.040
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Background: The analysis of blood for beta-sitosterol and campesterol is the measures of cholesterol absorption while lathosterol is a measure of cholesterol synthesis. Methods: The biological variability of beta-sitosterol, campesterol, and lathosterol was measured using liquid-chromatography tandem mass spectrometry from a cohort of 25 apparently healthy subjects, where blood was taken once every weeks for 6 weeks. The analytical, intra-individual, and group inter-individual variations (CVA, CV1, and CVG, respectively) were calculated. Results: Using absolute values, the CV1 for beta-sitosterol, campesterol, and lathosterol was 11.8%, 11.8%, and 22.5%, respectively, and the CVG was 28.5%, 28.8%, and 52.0%, respectively. This produced reference change values of about 24-36% for declining values and 32-47% for increasing values. The index of individuality was between 0.41 and 0.58, indicating that population based reference values are of little use for these biomarkers. The number of points needed for a homeostatic setpoint was 5 samples for beta-sitosterol and campesterol, and 19 samples for lathosterol. Similar findings were observed for values when normalized to total cholesterol. These results were higher than the biological variation for total, low density and high density cholesterol obtained from the literature. Results were essentially identical when sterol values were corrected to their respective total cholesterol concentration. Conclusions: The establishment of the biological variation for these biomarkers enables their use in the interpretation of results from clinical trials and lipid lowering treatment of patients at risk for cardiovascular disease in clinical practice. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:43 / 47
页数:5
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