Daytime triglyceride variability in men and women with different levels of triglyceridemia

被引:19
作者
Klop, Boudewijn [1 ]
Cohn, Jeffrey S. [2 ]
van Oostrom, Antonie J. H. H. M. [3 ]
van Wijk, Jeroen P. H. [4 ]
Birnie, Erwin
Cabezas, Manuel Castro [1 ]
机构
[1] Sint Franciscus Gasthuis Rotterdam, Dpts Internal Med, Rotterdam, Netherlands
[2] Heart Res Inst, Nutr & Metab Grp, Camperdown, NSW, Australia
[3] Sint Antonius Ziekenhuis Nieuwegein, Dpt Cardiol, Nieuwegein, Netherlands
[4] Univ Med Ctr Utrecht, Dpt Internal Med, Utrecht, Netherlands
关键词
Postprandial lipemia; Gender; Atherosclerosis; Variance; NONFASTING TRIGLYCERIDES; BIOLOGICAL VARIABILITY; POSTPRANDIAL LIPEMIA; LIPIDS; LIPOPROTEINS; APOLIPOPROTEINS; SERUM; HEALTHY; RISK; PROFILES;
D O I
10.1016/j.cca.2011.08.010
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: Triglyceride (TG) levels measured in either the fasting or non-fasting state predict the risk of cardiovascular disease (CVD). Since CVD risk assessment is affected by variability in TG, the aim of the study was to investigate intra-individual variability of non-fasting TG. Methods: Capillary triglyceride (cTG) levels were measured in 246 free-living individuals at six time-points during the day on three separate occasions. Intra-individual variability in cTG was assessed by calculating the standard deviation of three measures at each time-point. Subjects were analyzed by gender and by fasting TG level. Results: In the fasting state, intra-individual variability was similar in males and females (0.28 and 0.35 mmol/l, respectively), but increased significantly in male but not in female subjects during the day, i.e., 0.28 to 0.69, and 0.35 to 0.36 mmol/l, resp. Subjects with higher fasting TG levels had greater absolute variability in both fasting and non-fasting TG. Conclusions: The variability in non-fasting TG is greater in males and in individuals with higher levels of TG. Since greatest variability in non-fasting TG occurs very late in the day, it is unlikely to affect the assessment of CVD risk, which is based on a blood sample taken during daylight hours. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:2183 / 2189
页数:7
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