Letters to the Editor |
University of British Columbia, Vancouver, Canada
McGill University, Quebec, Canada
To the Editor:
In the last paragraph of this editorial (Arterioscler Thromb Vasc Biol. 2001;21:469470), Dr Eckel mentions that assays for apo B remain less than optimal and quotes our article that deals with standardization of the DAIS Study.1 In fact, after the decision was made on a common International Federation of Clinical Chemistry/World Health Organization standard for the 2 laboratories involved in DAIS, there was very little bias in the apo B values (see Figure 5A of our article). Apo B assays have been standardized2,3 and reference values established in both the United States and Canada (for a review, see Bhatnagar et al4).
Plasma apo B concentration, a measure of LDL particle number, has been shown in both epidemiological studies and prospective, double-blind, placebo controlled clinical trials to be related to clinical outcomes.57 In the Quebec Cardiovascular Study,5 apo B was the single most important lipid parameter that predicted cardiovascular events. Similarly, data from AFCAPS/TEXCAPS6 have demonstrated that although LDL cholesterol, HDL cholesterol, and apo B predict cardiac outcomes before therapy is initiated, the lipid levels and their ratios did not predict outcome on treatment, whereas apo B and the ratio of apo B to apo A1 did. Similarly, on treatment, apo B and apo A1 were the significant predictors in a secondary prevention study of van Lennep et al.7 This also fits well with observational data by Moss and colleagues8 in 1045 postinfarction patients. Target values have been established and accepted by the Canadian Cardiovascular Society.9
Although apo
Department of Medicine, Physiology, and Biophysics, University of Colorado Health Sciences Center, Denver, Colorado
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