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  Vol. 152 No. 8, August 1998 TABLE OF CONTENTS
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Utility of Direct Measurement of Low-Density Lipoprotein Cholesterol in Dyslipidemic Pediatric Patients

Baruch S. Ticho, MD, PhD; Ellis J. Neufeld, MD, PhD; Jane W. Newburger, MD, MPH; Neil Harris, MD; Annette Baker, RN; Nader Rifai, PhD

Arch Pediatr Adolesc Med. 1998;152:787-791.

Background  Low-density lipoprotein cholesterol (LDL-C) levels are the primary basis for treatment guidelines established for hyperlipidemic children and adolescents. Levels of LDL-C are commonly monitored by means of the Friedewald formula, an indirect calculation that requires an overnight fast. A new method has been developed for the direct measurement of LDL-C (DLDL-C) that does not require fasting. We evaluated the clinical utility of this method.

Design  We determined LDL-C concentrations simultaneously by the DLDL-C method, Friedewald equation, and {beta}-quantification (reference procedure).

Setting  Pediatric dyslipidemia clinic at Children's Hospital, Boston, Mass.

Patients  Ninety-two fasting hyperlipidemic pediatric patients.

Results  At the LDL-C concentration cutoffs commonly used for making therapeutic decisions, the DLDL-C method had a significant negative bias (P<=.05) and misclassified patients into incorrect treatment groups more often than the Friedewald method. The negative predictive value for the DLDL-C method was lower than that for the Friedewald method (P<=.05), and the cost of determining LDL-C level with the new method was 3 times greater.

Conclusions  The misclassification potential for LDL-C, and the assay costs, were greater for the DLDL-C method than for the Friedewald calculation. Despite the apparent advantages of the DLDL-C method, we conclude that for hyperlipidemic children the utility of this new method is not advantageous over the conventional Friedewald method. In some conditions, such as in diabetes or marked hypertriglyceridemia, the DLDL-C method may be useful.


From the Department of Cardiology (Drs Ticho and Newburger and Ms Baker), Division of Hematology (Dr Neufeld) and Laboratory Medicine (Drs Harris and Rifai), Children's Hospital, Dana Farber Cancer Institute, and the Departments of Pediatrics (Drs Ticho, Neufeld, and Newburger) and Pathology (Drs Harris and Rifai), Harvard Medical School, Boston, Mass. Dr Ticho is now with the Division of Pediatric Cardiology, Massachusetts General Hospital, Boston.



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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

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