The pharmacokinetics of caffeine and its dimethylxanthine metabolites in patients with chronic liver disease
- PMID: 2713214
- PMCID: PMC1379781
- DOI: 10.1111/j.1365-2125.1989.tb05352.x
The pharmacokinetics of caffeine and its dimethylxanthine metabolites in patients with chronic liver disease
Abstract
1. Serum and salivary concentrations of caffeine (1,3,7-trimethylxanthine) and its dimethylxanthine metabolites were measured in 10 healthy control subjects and in 19 patients with cirrhosis, for up to 96 h following a 400 mg oral caffeine load. 2. Serum and salivary caffeine concentrations correlated significantly (r = 0.954; P less than 0.001) and no significant differences were observed in the pharmacokinetic data derived from the respective concentration-time curves. 3. In the control subjects, basal salivary caffeine concentrations did not exceed 0.4 mg l-1. The median (range) basal salivary caffeine concentrations in patients with compensated cirrhosis (n = 10), 0.2 (0-0.7) mg l-1 and decompensated cirrhosis (n = 9), 0.7 (0-5.8) mg l-1, were not significantly different from control values, although three patients with decompensated cirrhosis had basal salivary caffeine values above 2.0 mg l-1. 4. In the patients with compensated cirrhosis, the median peak salivary caffeine concentration, 10.9 (8.2-16.5) mg l-1 was significantly greater than in controls, 7.1 (4.7-11.8) mg l-1 (P less than 0.01) and the median apparent volume of distribution was significantly reduced, 0.38 (0.19-0.49) vs 0.41 (0.23-0.63) l kg-1 (P less than 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)
Similar articles
-
[Use of the paraxanthine/caffeine ratio in the saliva of patients with liver cirrhosis].Cas Lek Cesk. 2001 Feb 1;140(2):51-3. Cas Lek Cesk. 2001. PMID: 11262908 Czech.
-
Population pharmacokinetics of caffeine and its metabolites theobromine, paraxanthine and theophylline after inhalation in combination with diacetylmorphine.Basic Clin Pharmacol Toxicol. 2005 Jan;96(1):71-9. doi: 10.1111/j.1742-7843.2005.pto960111.x. Basic Clin Pharmacol Toxicol. 2005. PMID: 15667599 Clinical Trial.
-
A simple useful method for the determination of hepatic function in patients with liver cirrhosis using caffeine and its three major dimethylmetabolites.Int J Clin Pharmacol Ther Toxicol. 1992 Sep;30(9):336-41. Int J Clin Pharmacol Ther Toxicol. 1992. PMID: 1428297
-
The toxicology of cocoa and methylxanthines: a review of the literature.Crit Rev Toxicol. 1982;9(4):275-312. doi: 10.3109/10408448209037495. Crit Rev Toxicol. 1982. PMID: 6765610 Review.
-
Physiologically based pharmacokinetic (PBPK) modeling of caffeine and theophylline in neonates and adults: implications for assessing children's risks from environmental agents.J Toxicol Environ Health A. 2004 Feb 27;67(4):297-329. doi: 10.1080/15287390490273550. J Toxicol Environ Health A. 2004. PMID: 14713563 Review.
Cited by
-
Caffeine promotes global spatial processing in habitual and non-habitual caffeine consumers.Front Hum Neurosci. 2013 Oct 17;7:694. doi: 10.3389/fnhum.2013.00694. eCollection 2013. Front Hum Neurosci. 2013. PMID: 24146646 Free PMC article.
-
Clinically significant pharmacokinetic interactions between dietary caffeine and medications.Clin Pharmacokinet. 2000 Aug;39(2):127-53. doi: 10.2165/00003088-200039020-00004. Clin Pharmacokinet. 2000. PMID: 10976659 Review.
-
Pharmacokinetics of Caffeine: A Systematic Analysis of Reported Data for Application in Metabolic Phenotyping and Liver Function Testing.Front Pharmacol. 2022 Feb 25;12:752826. doi: 10.3389/fphar.2021.752826. eCollection 2021. Front Pharmacol. 2022. PMID: 35280254 Free PMC article. Review.
-
Acute hyperammonaemia induces a sustained decrease in vigilance, which is modulated by caffeine.Metab Brain Dis. 2015 Feb;30(1):143-9. doi: 10.1007/s11011-014-9590-8. Epub 2014 Jul 24. Metab Brain Dis. 2015. PMID: 25052067
-
A Prediction Model of Drug Exposure in Cirrhotic Patients According to Child-Pugh Classification.Clin Pharmacokinet. 2015 Dec;54(12):1245-58. doi: 10.1007/s40262-015-0288-9. Clin Pharmacokinet. 2015. PMID: 26070946
References
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical