Int. Journal of Clinical Pharmacology and Therapeutics, Volume 38 - May (235 - 244)

Variation of CYP1A2-dependent caffeine metabolism during menstrual cycle in healthy women
M. Zaigler1,2, S. Rietbrock1,2, J. Szymanski2, J.S.E. Dericks-Tan3, A.H. Staib2, U. Fuhr1,2
1 Institute for Pharmacology, Clinical Pharmacology, Universität zu Köln, 2 Institute for Clinical Pharmacology, and 3 Department of Gynaecological Endocrinology, Centre for Gynaecology and Obstetrics, University Hospital, Frankfurt am Main, Germany

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DOI 10.5414/CPP38235

Abstract

Background and objectives: The activity of the human cytochrome P450 CYP1A2 is decreased by female sex hormones during pregnancy or treatment with oral contraceptives. However, the influence of menstrual cycle on CYP1A2 activity is not clear. Methods: CYP1A2 activity was monitored in 15 women (13 with confirmed ovulatory cycles, 2 smokers, age (mean ± SD) 27.8 ± 3.8 years, body mass index 23.8 ± 3.8 kg × m–2) using the specific substrate caffeine (mean doses 149 mg). After a run-in period started one week prior to expected onset of menses, daily saliva samples were taken 7.3 ± 0.7 hours after caffeine intake throughout the cycle, and caffeine clearance was estimated from the paraxanthine to caffeine ratio therein. Ovulation was confirmed by progesterone serum concentration above 3 ng/ml in the second half of the cycle. Results: Initial (day 2) caffeine clearance (n = 15, geometric mean) was 1.37 ml/min/kg body weight (coefficient of variation (CV) 48%). The ratio of caffeine clearance for the luteal (day –9 to –4 prior to onset of the next menses) to the follicular phase (days 5 – 10) was (n = 13, point estimate) 1.03 (90% CI 0.95 – 1.12), indicating that there was no difference in CYP1A2 activity between these cycle phases. The median intraindividual CV in ovulatory cycles (n = 13) was 23% (range 11% to 39%). As an additional finding, there was evidence for long-term fluctuations of CYP1A2 activity in most individuals. Conclusions: A dose adaptation according to the phase of menstrual cycle based on pharmacokinetics is not required for CYP1A2 substrates.

Author Details

Authors

Departments

  • 1 Institute for Pharmacology, Clinical Pharmacology, Universität zu Köln,
  • 2 Institute for Clinical Pharmacology, and
  • 3 Department of Gynaecological Endocrinology, Centre for Gynaecology and Obstetrics, University Hospital, Frankfurt am Main, Germany

Address

Prof. Dr. med. U. Fuhr; Institute for Pharmacology, Clinical Pharmacology, Universität zu Köln, Gleueler Straße 24, D-50931 Köln, Germany

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Citation

M. Zaigler, S. Rietbrock, J. Szymanski, J.S.E. Dericks-Tan, A.H. Staib and U. Fuhr. Variation of CYP1A2-dependent caffeine metabolism during menstrual cycle in healthy women. 2000; 38: 235-244. doi: 10.5414/CPP38235.

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