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Clinical Chemistry 40: 227-232, 1994;
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Clinical Chemistry, Vol 40, 227-232, Copyright © 1994 by American Association for Clinical Chemistry

Estimating and minimizing effects of biologic sources of variation by relative range when measuring the mean of serum lipids and lipoproteins

GR Cooper, SJ Smith, GL Myers, EJ Sampson and E Magid
Centers for Disease Control and Prevention, National Center for Environmental Health, Atlanta, GA 30341-3724.

Biologic intraindividual variation (CVb) is a major source of inaccuracy in current lipid and lipoprotein measurements. Metaanalysis has been used to estimate the average CVb of serum total cholesterol (TC), high-density lipoprotein cholesterol (HDLC), low-density lipoprotein cholesterol (LDLC), and triglyceride (TG). These CVb values are larger than the National Cholesterol Education Program-accepted and -proposed analytic (CVa) goals. Measuring serial specimens reduces the error in determination of the mean concentration used in classification of the patient by cutoff points. We show (a) a convenient technique, based on the relative range, to qualitatively estimate and interpret biologic variation of TC, HDLC, LDLC, and TG, and (b) the number of serial specimens required to meet a total variation goal for measurements of mean lipid and lipoprotein values. A total variation goal has been selected that can be met by two serial specimens for a majority of individuals.


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