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Lipids and Lipoproteins |
1
Minase Research Institute, Ono Pharmaceutical Company Ltd., 3-1-1 Sakurai, Shimamoto-cho, Osaka 618-8585, Japan.
2
Third Department of Medicine, Siga University of Medical
Science, Otsu 520-2152, Japan.
3
Department of Health Science, Siga University of Medical
Science, Otsu 520-2152, Japan.
4
Department of Laboratory Medicine, Hamamatsu University
School of Medicine, Hamamatsu 431-3124, Japan.
a Author for correspondence. Fax 8175-962-9314.
We have developed an enzyme immunoassay for mevalonic acid (MVA), using a specific monoclonal antibody. The intra- and interassay coefficients of variation calculated on two urine samples were 3.3% and 3.4%, respectively, in the intraassay precision test and 3.5% and 6.9% in the interassay evaluation. Pravastatin, a 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase inhibitor, was administered to nine healthy men, and in all cases, their MVA excretion rates then decreased. The more MVA that was excreted in the urine before the pravastatin administration, the greater a reduction of MVA excretion was observed. The daily MVA excretions in healthy men (n = 120) and women (n = 105) were 2.32 µmol/day (SD, 0.82 µmol/day) and 1.85 µmol/day (SD, 0.47 µmol/day), respectively. In streptozotocin-induced diabetic rats (n = 14), the plasma cholesterol concentrations and MVA excretion rates were increased, and a positive correlation was observed between the plasma cholesterol and the urinary MVA concentrations.
The following articles in journals at HighWire Press have cited this article:
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G. S. Saini, T. A. Wani, A. Gautam, B. Varshney, T. Ahmed, K. S. Rajan, K. K. Pillai, and J. K. Paliwal Validation of the LC-MS/MS method for the quantification of mevalonic acid in human plasma and determination of the matrix effect J. Lipid Res., October 1, 2006; 47(10): 2340 - 2345. [Abstract] [Full Text] [PDF] |
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