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Clinical Chemistry 45: 1981-1987, 1999;
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(Clinical Chemistry. 1999;45:1981-1987.)
© 1999 American Association for Clinical Chemistry, Inc.


Articles

Ratio of Remnant-like Particle-Cholesterol to Serum Total Triglycerides Is an Effective Alternative to Ultracentrifugal and Electrophoretic Methods in the Diagnosis of Familial Type III Hyperlipoproteinemia

Tao Wang1,a, Katsuyuki Nakajima1, Elizabeth Teng Leary2, G. Russ Warnick2, Jeffrey S. Cohn3, Paul N. Hopkins4, Lily L. Wu4, Donald D. Cilla1, Jianhua Zhong1 and Richard J. Havel5

1 Otsuka America Pharmaceutical, Inc., 2440 Research Blvd., Rockville, MD 20850.

2 Pacific Biometrics, Inc. Seattle, WA 98119.

3 Clinical Research Institute of Montreal, Montreal, Quebec, Canada H2W 1R7.

4 University of Utah, Salt Lake City, UT 84108.

5 Cardiovascular Research Institute, University of California, San Francisco, CA 94143.

6 All results are presented in SI units. To convert from SI units to "mg/dL", multiply the values by the following conversion factors: 38.61 for cholesterol, 88.50 for triglyceride, and 0.436 for the cholesterol (VLDL-C or RLP-C)-to-total triglyceride ratio. The upper limits of the reference intervals for the ratios of VLDL-C and RLP-C to total triglyceride are 0.69 and 0.23, respectively, for the SI values (or 0.30 and 0.10, respectively, for mg/dL).
a Author for correspondence. Fax 301-721-7213; e-mail TAOW{at}MOCR.OAPI.com

Background: Familial type III hyperlipoproteinemia (HLP) is characterized by the presence of ß-migrating VLDL (ß-VLDL) and increased risk of cardiovascular disease. Assessment of plasma ß-VLDL is achieved by measuring the ratio of VLDL-cholesterol (VLDL-C) to total plasma triglycerides (TGs) or by detecting ß-VLDL in total VLDL. The objective of this study was to compare the clinical utility of the ratio of remnant-like particle-cholesterol (RLP-C) to total TGs with that of the current methods for diagnosing type III HLP.

Methods: Detection of ß-VLDL by electrophoresis of VLDL was used to define type III HLP. Twenty-eight patients with type III HLP and 43 subjects lacking ß-VLDL were investigated. Fasting TG concentrations were >2.26 mmol/L in all subjects. Subjects were separated into three groups: group 1, serum total cholesterol <=5.18 mmol/L (n = 11); group 2, total cholesterol >5.18 mmol/L and TGs between 2.26 and 9.04 mmol/L (n = 51); and group 3, TGs >9.04 mmol/L (n = 9).

Results: In group 2, a RLP-C-to-total TG molar ratio >=0.23 (>=0.10 when using mg/dL) and a VLDL-C-to-total TG molar ratio >=0.69 (>=0.30 when using mg/dL) correctly classified 94% and 90% of the subjects, respectively. The utility of the RLP-C-to-total TG ratio in diagnosing type III HLP decreased in patients in the other two groups.

Conclusion: When used in an appropriate target population, the RLP-C-to-total TG ratio is a convenient and effective alternative to ultracentrifugal and electrophoretic methods for diagnosing type III HLP.




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