Evaluation of caffeine as a test drug for CYPIA2, NAT2 and CYP2E1 phenotyping in man by in vivo versus in vitro correlations

Caffeine is used to phenotype subjects in vivo for the cytochrome P450 isoforms CYP1A2 and CYP2E1, and for N-acetyltransferase type 2 (NAT2), However, how much of the variation in phenotyping parameters may be attributed to variations in CYP1A2 and CYP2E1 activities has not been determined, Therefore, this study intraindividually compared enzyme activities and/or content in liver samples with pharmacokinetic parameters of caffeine in vivo after administration of a test dose in 25 patients undergoing hepatectomy, Parameters measured in vitro were the high affinity components of caffeine 3-demethylation and phenacetin O-deethylation, microsomal CYP1A2 and CYP2E1 immunoreactivity, and cytosolic sulfamethazine N-acetylation. Caffeine parameters in vivo included caffeine clearance from plasma and/or saliva, paraxanthine/caffeine ratios in plasma and saliva, plasma theophylline/caffeine ratio, and several metabolite ratios from spot urine sampled 6 h postdose, Correlations between parameters were determined using weighted linear regression analyses, Caffeine clearance and paraxanthine/caffeine ratios correlated most highly to intrinsic clearance of caffeine 3-demethylation and to CYP1A2 immunoreactivity (r = 0.58-0.82), whereas urinary CYP1A2 ratios correlated less strongly with CYP1A2 parameters in vitro, Assignment of acetylator phenotype by urinary NAT2 ratios was concordant with sulfamethazine N-acetylation in vitro, In contrast to CYP1A2 paramters in vitro, CYP2E1 immunoreactivity was not related to the theophylline/caffeine plasma ratio, CYP1A2 activity, thus, is the major determinant of caffeine clearance and the paraxanthine/caffeine ratios in vivo, of which the saliva ratio 6 h postdose appears as the most advantageous parameter, The results confirm that phenotyping using caffeine provides valid estimates of CYP1A2 and NAT2, activity.