Clinical Chemistry
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Clinical Chemistry 43: 1904-1912, 1997;
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(Clinical Chemistry. 1997;43:1904-1912.)
© 1997 American Association for Clinical Chemistry, Inc.


Articles

Measurement of low-density lipoprotein particle size by high-performance gel-filtration chromatography

Peter G. Scheffer1,a, Stephan J. L. Bakker2, Robert J. Heine2 and Tom Teerlink1

Departments of
1 Clinical Chemistry and
2 Endocrinology, Research Institute for Endocrinology, Reproduction and Metabolism, Academic Hospital Vrije Universiteit, P.O. Box 7057, 1007 MB Amsterdam, The Netherlands.
a Author for correspondence. Fax 31-20-4443895.

We describe a new technique for measuring LDL size by high-performance gel-filtration chromatography (HPGC). LDL was subjected to chromatography, and the column effluent was monitored at 280 nm. The retention time of the LDL peak was used to calculate the LDL diameter. We compared the HPGC method with gradient gel electrophoresis (GGE) on 2–10% nondenaturing polyacrylamide gels. In a group of 60 non-insulin-dependent diabetes mellitus patients, LDL size as measured by HPGC and GGE was highly correlated (r = 0.88, P <0.001). Good reproducibility, high precision, and the possibility of analyzing large series of samples are the main advantages of the automated HPGC method. Within-run and between-run CV for LDL size measured by HPGC were <0.1% and 0.2%, respectively. There was a significant inverse association between LDL size measured by HPGC and the logarithm of plasma triglycerides (r = -0.84, P <0.001), and a significant positive association with the LDL free cholesterol/protein ratio (r = 0.89, P <0.001).




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Combined data from LDL composition and size measurement are compatible with a discoid particle shape
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Copyright © 1997 by the American Association for Clinical Chemistry.