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First, clinical settings were different; the previous report was on 13 healthy persons, while our study represents real clinical settings where distinct kinds of medications were concomitantly used.
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The disproportionate increase from year 4 to year 5 can be attributed to the withdrawal from the study of some subjects who had completed the five years of follow-up and who could have proceeded further but did not wish to do so.
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In this study, we have assessed the impact of inherent demographic characteristics in conjunction with coexisting diseases and genetic polymorphisms using a population pharmacokinetic analysis utilizing a nonlinear mixed effect model to identify potential covariates that explain the variability in pharmacokinetic properties of acid and lactone forms of atorvastatin.
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Hjalmarson (cochairs), members of the executive committee, the authors, and one AstraZeneca monitor from each of the 21 participating countries (nonvoting; for names see Kjekshus et al.
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